Machine perfusion

Machine perfusion (MP) is a technique used in organ transplantation as a means of preserving the organs which are to be transplanted. To some degree, it emulates natural perfusion. So far it has mainly been used in kidney transplantation. It is an alternative to cold storage (CS). Its clinical and cost-effectiveness are still subject to research.[1]

Hypothermic perfusion has given the longest storage time for canine kidneys with the best result being 8 day storage.[2] This experimental model used a storage temperature of 8 °C and a Plasma Protein Fraction (PPF) based perfusate.[3] The octanoic acid content of PPF was found to influence the results of preservation in five-day storage.[4] Both octanoic acid and oleic acid stimulated oxygen consumption to a similar degree during hypothermic perfusion[5] suggesting that the detrimental effect of octanoic acid was due to direct metabolic stimulation rather than uncoupling of oxidatative phosphorylation.[6]

History of kidney preservation techniques

An essential preliminary to the development of kidney storage and transplantation was the work of Carrel in developing methods for vascular anastomosis.[7] Carrel went on to describe the first kidney transplants, which were performed in dogs in 1902; Ullman[8] independently described similar experiments in the same year. In these experiments kidneys were transplanted without there being any attempt at storage.

The crucial step in making in vitro storage of kidneys possible, was the demonstration by Fuhrman in 1943,[9] of a reversible effect of hypothermia on the metabolic processes of isolated tissues. Prior to this, kidneys had been stored at normal body temperatures using blood or diluted blood perfusates,[10][11] but no successful reimplantations had been made. Fuhrman showed that slices of rat kidney cortex and brain withstood cooling to 0.2 °C for one hour at which temperature their oxygen consumption was minimal. When the slices were rewarmed to 37 °C their oxygen consumption recovered to normal.

The beneficial effect of hypothermia on ischaemic intact kidneys was demonstrated by Owens in 1955 [12] when he showed that, if dogs were cooled to 23-26 °C, and their thoracic aortas were occluded for 2 hours, their kidneys showed no apparent damage when the dogs were rewarmed. This protective effect of hypothermia on renal ischaemic damage was confirmed by Bogardus [13] who showed a protective effect from surface cooling of dog kidneys whose renal pedicles were clamped in situ for 2 hours. Moyer [14] demonstrated the applicability of these dog experiments to the human, by showing the same effect on dog and human kidney function from the same periods of hypothermic ischaemia.

It was not until 1958 that it was shown that intact dog kidneys would survive ischaemia even better if they were cooled to lower temperatures. Stueber [15] showed that kidneys would survive in situ clamping of the renal pedicle for 6 hours if the kidneys were cooled to 0-5 °C by being placed in a cooling jacket, and Schloerb [16] showed that a similar technique with cooling of heparinised dog kidneys to 2-4 °C gave protection for 8 hours but not 12 hours. Schloerb also attempted in vitro storage and auto-transplantation of cooled kidneys, and had one long term survivor after 4 hours kidney storage followed by reimplantation and immediate contralateral nephrectomy. He also had a near survivor, after 24-hour kidney storage and delayed contralateral nephrectomy, in a dog that developed a late arterial thrombosis in the kidney.

These methods of surface cooling were improved by the introduction of techniques in which the kidney's vascular system was flushed out with cold fluid prior to storage. This had the effect of increasing the speed of cooling of the kidney and removed red cells from the vascular system. Kiser [17] used this technique to achieve successful 7 hours in vitro storage of a dog kidney, when the kidney had been flushed at 5 °C with a mixture of dextran and diluted blood prior to storage. In 1960 Lapchinsky [18] confirmed that similar storage periods were possible, when he reported 8 dogs surviving after their kidneys had been stored at 2-4 °C for 28 hours, followed by auto-transplantation and delayed contralateral nephrectomy. Although Lapchinsky gave no details in his paper, Humphries [19] reported that these experiments had involved cooling the kidneys for 1 hour with cold blood, and then storage at 2-4 °C, followed by rewarming of the kidneys over 1 hour with warm blood at the time of reimplantation. The contralateral nephrectomies were delayed for 2 months.

Humphries [20] developed this storage technique by continuously perfusing the kidney throughout the period of storage. He used diluted plasma or serum as the perfusate and pointed out the necessity for low perfusate pressures to prevent kidney swelling, but admitted that the optimum values for such variables as perfusate temperature, Po2, and flow, remained unknown. His best results, at this time, were 2 dogs that survived after having their kidneys stored for 24 hours at 4-10 °C followed by auto-transplantation and delayed contralateral nephrectomy a few weeks later.

Calne [21] challenged the necessity of using continuous perfusion methods by demonstrating that successful 12-hour preservation could be achieved using much simpler techniques. Calne had one kidney supporting life even when the contralateral nephrectomy was performed at the same time as the reimplantation operation. Calne merely heparinised dog kidneys and then stored them in iced solution at 4 °C. Although 17-hour preservation was shown to be possible in one experiment when nephrectomy was delayed, no success was achieved with 24-hour storage.

The next advance was made by Humphries [22] in 1964, when he modified the perfusate used in his original continuous perfusion system, and had a dog kidney able to support life after 24-hour storage, even when an immediate contralateral nephrectomy was performed at the same time as the reimplantation. In these experiments autogenous blood, diluted 50% with Tis-U-Sol solution at 10 °C, was used as the perfusate. The perfusate pressure was 40 mm Hg and perfusate pH 7.11-7.35 (at 37 °C). A membrane lung was used for oxygenation to avoid damaging the blood.

In attempting to improve on these results Manax [23] investigated the effect of hyperbaric oxygen, and found that successful 48 hour storage of dog kidneys was possible at 2 °C without using continuous perfusion, when the kidneys were flushed with a dextran/Tis-U-Sol solution before storage at 7.9 atmospheres pressure, and if the contralateral nephrectomy was delayed till 2 to 4 weeks after reimplantation. Manax postulated that hyperbaric oxygen might work either by inhibiting metabolism or by aiding diffusion of oxygen into the kidney cells, but he reported no control experiments to determine whether other aspects of his model were more important than hyperbaria.

A marked improvement in storage times was achieved by Belzer in 1967 [24] when he reported successful 72-hour kidney storage after returning to the use of continuous perfusion using a canine plasma based perfusate at 8-12°C. Belzer [25] found that the crucial factor in permitting uncomplicated 72-hour perfusion was cryoprecipitation of the plasma used in the perfusate to reduce the amount of unstable lipo-proteins which otherwise precipitated out of solution and progressively obstructed the kidney's vascular system. A membrane oxygenator was also used in the system in a further attempt to prevent denaturation of the lipo-proteins because only 35% of the lipo-proteins were removed by cryo-precipitation. The perfusate comprised 1 litre of canine plasma, 4 mEq of magnesium sulphate, 250 ml of dextrose, 80 units of insulin, 200,000 units of penicillin and 100 mg of hydrocortisone. Besides being cryo-precipitated, the perfusate was pre-filtered through a 0.22 micron filter immediately prior to use. Belzer used a perfusate pH of 7.4-7.5, a Po2 of 150–190 mm Hg, and a perfusate pressure of 50–80 mm Hg systolic, in a machine that produced a pulsatile perfusate flow. Using this system Belzer had 6 dogs surviving after their kidneys had been stored for 72 hours and then reimplanted, with immediate contralateral nephrectomies being performed at the reimplantation operations.

Belzer's use of hydrocortisone as an adjuvant to preservation had been suggested by Lotke's work with dog kidney slices,[26] in which hydrocortisone improved the ability of slices to excrete PAH and oxygen after 30 hour storage at 2-4 °C; Lotke suggested that hydrocortisone might be acting as a lysosomal membrane stabiliser in these experiments. The other components of Belzer's model were arrived at empirically. The insulin and magnesium were used partially in an attempt to induce artificial hibernation, as Suomalainen [27] found this regime to be effective in inducing hibernation in natural hibernators. The magnesium was also provided as a metabolic inhibitor following Kamiyama's demonstration [28] that it was an effective agent in dog heart preservation. A further justification for the magnesium was that it was needed to replace calcium which had been bound by citrate in the plasma.

Belzer [29] demonstrated the applicability of his dog experiments to human kidney storage when he reported his experiences in human kidney transplantation using the same storage techniques as he had used for dog kidneys. He was able to store kidneys for up to 50 hours with only 8% of patients requiring post operative dialysis when the donor had been well prepared.

In 1968 Humphries [30] reported 1 survivor out of 14 dogs following 5 day storage of their kidneys in a perfusion machine at 10 °C, using a diluted plasma medium containing extra fatty acids. However, delayed contralateral nephrectomy 4 weeks after reimplantation was necessary in these experiments to achieve success, and this indicated that the kidneys were severely injured during storage.

In 1969 Collins [31] reported an improvement in the results that could be achieved with simple non perfusion methods of hypothermic kidney storage. He based his technique on the observation by Keller [32] that the loss of electrolytes from a kidney during storage could be prevented by the use of a storage fluid containing cations in quantities approaching those normally present in cells. In Collins' model, the dogs were well hydrated prior to nephrectomy, and were also given mannitol to induce a diuresis. Phenoxybenzamine, a vasodilator and lysozomal enzyme stabiliser,[33][34] was injected into the renal artery before nephrectomy. The kidneys were immersed in saline immediately after removal, and perfused through the renal artery with 100-150 ml of a cold electrolyte solution from a height of 100 cm. The kidneys remained in iced saline for the rest of the storage period. The solution used for these successful cold perfusions imitated the electrolyte composition of intracellular fluids by containing large amounts of potassium and magnesium. The solution also contained glucose, heparin, procaine and phenoxybenzamine. The solution's pH was 7.0 at 25 °C. Collins was able to achieve successful 24-hour storage of 6 kidneys, and 30 hour storage of 3 kidneys, with the kidneys functioning immediately after reimplantation, despite immediate contralateral nephrectomies. Collins emphasised the poor results obtained with a Ringer's solution flush, in finding similar results with this management when compared with kidneys treated by surface cooling alone. Liu [35] reported that Collins' solution could give successful 48 hour storage when the solution was modified by the inclusion of amino acids and vitamins. However, Liu performed no control experiments to show that these modifications were crucial.

Difficulty was found by other workers in repeating Belzer's successful 72-hour perfusion storage experiments. Woods [36] was able to achieve successful 48 hour storage of 3 out of 6 kidneys when he used the Belzer additives with cryoprecipitated plasma as the perfusate in a hypothermic perfusion system, but he was unable to extend the storage time to 72 hours as Belzer had done. However, Woods [37] later achieved successful 3 and 7 days storage of dog kidneys. Woods had modified Belzer's perfusate by the addition of 250 mg of methyl prednisolone, increased the magnesium sulphate content to 16.2 mEq and the insulin to 320 units. Six of 6 kidneys produced life sustaining function when they were reimplanted after 72 hours storage despite immediate contralateral nephrectomies; 1 of 2 kidneys produced life sustaining function after 96 hours storage, 1 of 2 after 120 hours storage, and 1 of 2 after 168 hours storage. Perfusate pressure was 60 mm Hg with a perfusate pump rate of 70 beats per minute, and perfusate pH was automatically maintained at 7.4 by a C02 titrator. Woods stressed the importance of hydration of the donor and recipient animals. Without the methyl prednisolone, Woods found vessel fragility to be a problem when storage times were longer than 48 hours.

A major simplification to the techniques of hypothermic perfusion storage was made by Johnson [38] and Claes in 1972 [39] with the introduction of an albumin based perfusate. This perfusate eliminated the need for the manufacture of the cryoprecipitated and millipore filtered plasma used by Belzer. The preparation of this perfusate had been laborious and time consuming, and there was the potential risk from hepatitis virus and cytotoxic antibodies. The absence of lipo-proteins from the perfusate meant that the membrane oxygenator could be eliminated from the perfusion circuit, as there was no need to avoid a perfusate/air interface to prevent precipitation of lipo-proteins. Both workers used the same additives as recommended by Belzer.

The solution that Johnson used was prepared by the Blood Products Laboratory (Elstree: England) by extracting heat labile fibrinogen and gamma globulins from plasma to give a plasma protein fraction (PPF) solution. The solution was incubated at 60 °C for 10 hours to inactivate the agent of serum hepatitis.[40] The result was a 45 g/l human albumin solution containing small amounts of gamma and beta globulins which was stable between 0 °C and 30 °C for 5 years.[41] PPF contained 2.2 mmol/l of free fatty acids.[42]

Johnson's [43] experiments were mainly concerned with the storage of kidneys that had been damaged by prolonged warm injury. However, in a control group of non-warm injured dog kidneys, Johnson showed that 24-hour preservation was easily achieved when using a PPF perfusate, and he described elsewhere [44] a survivor after 72 hours perfusion and reimplantation with immediate contralateral nephrectomy. With warm injured kidneys, PPF perfusion gave better results than Collins' method, with 6 out of 6 dogs surviving after 40 minutes warm injury and 24-hour storage followed by reimplantation of the kidneys and immediate contralateral nephrectomy. Potassium, magnesium, insulin, glucose, hydrocortisone and ampicillin were added to the PPF solution to provide an energy source and to prevent leakage of intracellular potassium. Perfusate temperature was 6 °C, pressure 40–80 mm Hg, and Po2 200–400 mm Hg. The pH was maintained between 7.2 and 7.4.

Claes [45] used a perfusate based on human albumin (Kabi: Sweden) diluted with saline to a concentration of 45 g/l. Claes preserved 4 out of 5 dog kidneys for 96 hours with the kidneys functioning immediately after reimplantation despite immediate contralateral nephrectomies. Claes also compared this perfusate with Belzer's cryoprecipitated plasma in a control group and found no significant difference between the function of the reimplanted kidneys in the two groups.

The only other group besides Woods' to report successful 7 day storage of kidneys was Liu and Humphries [46] in 1973. They had 3 out of 7 dogs surviving, after their kidneys had been stored for 7 days followed by reimplantation and immediate contralateral nephrectomy. Their best dog had a peak post reimplantation creatinine of 50 mg/l (0.44 mmol/l). Liu used well hydrated dogs undergoing a mannitol diuresis and stored the kidneys at 9 °C – 10 °C using a perfusate derived from human PPF. The PPF was further fractionated by using a highly water-soluble polymer (Pluronic F-38), and sodium acetyl tryptophanate and sodium caprylate were added to the PPF as stabilisers to permit pasteurisation. To this solution were added human albumin, heparin, mannitol, glucose, magnesium sulphate, potassium chloride, insulin, methyl prednisolone, carbenicillin, and water to adjust the osmolality to 300-310 mosmol/kg. The perfusate was exchanged after 3.5 days storage. Perfusate pressure was 60 mm Hg or less, at a pump rate of 60 per minute. Perfusate pH was 7.12–7.32 (at 37 °C), Pco2 27–47 mm Hg, and Po2 173–219 mm Hg. In a further report on this study Humphries [47] found that when the experiments were repeated with a new batch of PPF no survivors were obtained, and histology of the survivors from the original experiment showed glomerular hypercellularity which he attributed to a possible toxic effect of the Pluronic polymer.

Joyce and Proctor [48] reported the successful use of a simple dextran based perfusate for 72-hour storage of dog kidneys. 10 out of 17 kidneys were viable after reimplantation and immediate contralateral nephrectomy. Joyce used non pulsatile perfusion at 4 °C with a perfusate containing Dextran 70 (Pharmacia) 2.1%, with additional electrolytes, glucose (19.5 g/l), procaine and hydrocortisone. The perfusate contained no plasma or plasma components. Perfusate pressure was only 30 cm H20, pH 7.34-7.40 and Po2 250–400 mm Hg. This work showed that, for 72-hour storage, no nutrients other than glucose were needed, and low perfusate pressures and flows were adequate.

In 1973 Sacks [49] showed that simple ice storage could be successfully used for 72-hour storage when a new flushing solution was used for the initial cooling and flush out of the kidney. Sacks removed kidneys from well hydrated dogs that were diuresing after a mannitol infusion, and flushed the kidneys with 200 ml of solution from a height of 100 cm. The kidneys were then simply kept at 2 °C for 72 hours without further perfusion. Reimplantation was followed by immediate contralateral nephrectomies. The flush solution was designed to imitate intracellular fluid composition and contained mannitol as an impermeable ion to further prevent cell swelling. The osmolality of the solution was 430 mosmol/kg and its pH was 7.0 at 2 °C. The additives that had been used by Collins (dextrose, phenoxybenzamine, procaine and heparin) were omitted by Sacks.

These results have been equalled by Ross [50] who also achieved successful 72-hour storage without using continuous perfusion, although he was unable to reproduce Collins' or Sacks' results using the original Collins' or Sacks' solutions. Ross's successful solution was similar in electrolyte composition to intracellular fluid with the addition of hypertonic citrate and mannitol. No phosphate, bicarbonate, chloride or glucose were present in the solution; the osmolality was 400 mosmol/kg and the pH 7.1. Five of 8 dogs survived reimplantation of their kidneys and immediate contralateral nephrectomy, when the kidneys had been stored for 72 hours after having been flushed with Ross's solution; but Ross was unable to achieve 7 day storage with this technique even when delayed contralateral nephrectomy was used.

The requirements for successful 72-hour hypothermic perfusion storage have been further defined by Collins who showed that pulsatile perfusion was not needed if a perfusate pressure of 49 mm Hg was used, and that 7 °C was a better temperature for storage than 2 °C or 12 °C.[51][52] He also compared various perfusate compositions and found that a phosphate buffered perfusate could be used successfully, so eliminating the need for a carbon dioxide supply.[53] Grundmann [54] has also shown that low perfusate pressure is adequate. He used a mean pulsatile pressure of 20 mm Hg in 72-hour perfusions and found that this gave better results than mean pressures of 15, 40, 50 or 60 mm Hg.

Successful storage up to 8 days was reported by Cohen [55] using various types of perfusate – with the best result being obtained when using a phosphate buffered perfusate at 8 °C. Inability to repeat these successful experiments was thought to be due to changes that had been made in the way that the PPF was manufactured with higher octanoic acid content being detrimental. Octanoic acid was shown to be able to stimulate metabolic activity during hypothermic perfusion[56] and this might be detrimental.

Nature of kidney preservation injury

Structural injury

The structural changes that occur during 72-hour hypothermic storage of previously uninjured kidneys have been described by Mackay [57] who showed how there was progressive vacuolation of the cytoplasm of the cells which particularly affected the proximal tubules. On electron microscopy the mitochondria were seen to become swollen with early separation of the internal cristal membranes and later loss of all internal structure. Lysosomal integrity was well preserved until late, and the destruction of the cell did not appear to be caused by lytic enzymes because there was no more injury immediately adjacent to the lysosomes than in the rest of the cell.

Woods [58][59] and Liu [60] – when describing successful 5 and 7 day kidney storage - described the light microscopic changes seen at the end of perfusion and at post mortem, but found few gross abnormalities apart from some infiltration with lymphocytes and occasional tubular atrophy.

The changes during short perfusions of human kidneys prior to reimplantation have been described by Hill [61] who also performed biopsies 1 hour after reimplantation. On electron microscopy Hill found endothelial damage which correlated with the severity of the fibrin deposition after reimplantation. The changes that Hill saw in the glomeruli on light microscopy were occasional fibrin thrombi and infiltration with polymorphs. Hill suspected that these changes were an immunologically induced lesion, but found that there was no correlation between the severity of the histological lesion and the presence or absence of immunoglobulin deposits.

There are several reports of the analysis of urine produced by kidneys during perfusion storage. Kastagir [62] analysed urine produced during 24-hour perfusion and found it to be an ultrafiltrate of the perfusate, Scott [63] found a trace of protein in the urine during 24-hour storage, and Pederson [64] found only a trace of protein after 36 hours perfusion storage. Pederson mentioned that he had found heavy proteinuria during earlier experiments. Woods [65] noted protein casts in the tubules of viable kidneys after 5 day storage, but he did not analyse the urine produced during perfusion. In Cohen’s study [66] there was a progressive increase in urinary protein concentration during 8 day preservation until the protein content of the urine equalled that of the perfusate. This may have been related to the swelling of the glomerular basement membranes and the progressive fusion of epithelial cell foot processes that was also observed during the same period of perfusion storage.

Mechanisms of injury

The mechanisms that damage kidneys during hypothermic storage can be sub-divided as follows:

  1. Injury to the metabolic processes of the cell caused by:
    1. Cold
    2. Anoxia when the kidney is warm both before and after the period of hypothermic storage.
    3. Failure to supply the correct nutrients.
    4. Toxin accumulation in the perfusate.
    5. Toxic damage from the storage fluid.
    6. Washout of essential substrates from the kidney cells.
  2. Injury to nuclear DNA.
  3. Mechanical injury to the vascular system of the kidney during hypothermic perfusion.
  4. Post reimplantation injury.

Metabolic injury

Cold

At normal temperatures pumping mechanisms in cell walls retain intracellular potassium at high levels and extrude sodium. If these pumps fail sodium is taken up by the cell and potassium lost. Water follows the sodium passively and results in swelling of the cells. The importance of this control of cell swelling was demonstrated by McLoughlin [67] who found a significant correlation between canine renal cortical water content and the ability of kidneys to support life after 36 hour storage. The pumping mechanism is driven by the enzyme system known as Na+K+- activated ATPase [68] and is inhibited by cold. Levy [69] found that metabolic activity at 10 °C, as indicated by oxygen consumption measurements, was reduced to about 5% of normal and, because all enzyme systems are affected in a similar way by hypothermia, ATPase activity is markedly reduced at 10 °C.

There are, however, tissue and species differences in the cold sensitivity of this ATPase which may account for the differences in the ability of tissues to withstand hypothermia. Martin [70] has shown that in dog kidney cortical cells some ATPase activity is still present at 10 °C but not at 0 °C. In liver and heart cells activity was completely inhibited at 10 °C and this difference in the cold sensitivity of ATPase correlated with the greater difficulty in controlling cell swelling during hypothermic storage of liver and heart cells. A distinct ATPase is found in vessel walls, and this was shown by Belzer [71] to be completely inhibited at 10 °C, when at this temperature kidney cortical cells ATPase is still active. These experiments were performed on aortic endothelium, but if the vascular endothelium of the kidney has the same properties, then vascular injury may be the limiting factor in prolonged kidney storage.

Willis [72] has shown how hibernators derive some of their ability to survive low temperatures by having a Na+K+-ATPase which is able to transport sodium and potassium actively across their cell membranes, at 5 °C, about six times faster than in non-hibernators; this transport rate is sufficient to prevent cell swelling.

The rate of cooling of a tissue may also be significant in the production of injury to enzyme systems. Francavilla [73] showed that when liver slices were rapidly cooled (immediate cooling to 12 °C in 6 minutes) anaerobic glycolysis, as measured on rewarming to 37 °C, was inhibited by about 67% of the activity that was demonstrated in slices that had been subjected to delayed cooling. However, dog kidney slices were less severely affected by the rapid cooling than were the liver slices.

Anoxia

All cells require ATP as an energy source for their metabolic activity. The kidney is damaged by anoxia when kidney cortical cells are unable to generate sufficient ATP under anaerobic conditions to meet the needs of the cells. When excising a kidney some anoxia is inevitable in the interval between dividing the renal artery and cooling the kidney. It has been shown by Bergstrom [74] that 50% of a dog's kidney's cortical cells ATP content is lost within 1 minute of clamping the renal artery, and similar results were found by Warnick [75] in whole mice kidneys, with a fall in cellular ATP by 50% after about 30 seconds of warm anoxia. Warnick and Bergstrom also showed that cooling the kidney immediately after removal markedly reduced any further ATP loss. When these non warm-injured kidneys were perfused with oxygenated hypothermic plasma, ATP levels were reduced by 50% after 24-hour storage and, after 48 hours, mean tissue ATP levels were a little higher than this indicating that synthesis of ATP had occurred. Pegg [76] has shown that rabbit kidneys can resynthesize ATP after a period of perfusion storage following warm injury, but no resynthesis occurred in non warm-injured kidneys.

Warm anoxia can also occur during reimplantation of the kidney after storage. Lannon [77] showed, by measurements of succinate metabolism, how the kidney was more sensitive to a period of warm hypoxia occurring after storage than to the same period of warm hypoxia occurring immediately prior to storage.

Lack of essential nutrients

Active metabolism of glucose with production of bicarbonate has been demonstrated by Pettersson[78] and Cohen.[79]

Pettersson studies [80] were on the metabolism of glucose and fatty acids by kidneys during 6 day hypothermic perfusion storage and he found that the kidneys consumed glucose at 4.4 μmol/g/day and fatty acids at 5.8 μmol/g/day. In Cohen’s study [81] the best 8 day stored kidneys consumed glucose at the rate of 2.3 μmol/g/day and 4.9 μmol/g/day respectively which made it likely that they were using fatty acids at similar rates to Pettersson's dogs' kidneys. The constancy of both the glucose consumption rate and the rate of bicarbonate production implied that no injury was affecting the glycolytic enzyme or carbonic anhydrase enzyme systems.

Lee [82] showed that fatty acids were the preferred substrate of the rabbit's kidney cortex at normothermic temperatures, and glucose the preferred substrate for the medullary cells which normally metabolise anaerobically. Abodeely [83] showed that both fatty acids and glucose could be utilised by the outer medulla of the rabbit's kidney but that glucose was used preferentially. At hypothermia the metabolic needs of the kidney are much reduced but measurable consumption of glucose, fatty acids and ketone bodies occurs. Horsburgh [84] showed that lipid is utilised by hypothermic kidneys, with palmitate consumption being 0-15% of normal in the rat kidney cortex at 15 °C. Pettersson [85] showed that, on a molar basis, glucose and fatty acids were metabolised by hypothermically perfused kidneys at about the same rates. The cortex of the hypothermic dog kidney was shown by Huang [86] to lose lipid (35% loss of total lipid after 24 hours) unless oleate was added to the kidney perfusate. Huang commented that this loss could affect the structure of the cell and that the loss also suggested that the kidney was utilising fatty acid. In a later publication Huang [87] showed that dog kidney cortex slices metabolised fatty acids, but not glucose, at 10 °C.

Even if the correct nutrients are provided, they may be lost by absorption into the tubing of the preservation system. Lee [88] demonstrated that silicone rubber (a material used extensively in kidney preservation systems) absorbed 46% of a perfusate's oleic acid after 4 hours of perfusion.

Toxin accumulation

Abouna [89] showed that ammonia was released into the perfusate during 3 day kidney storage, and suggested that this might be toxic to the kidney cells unless removed by frequent replacement of the perfusate. Some support for the use of perfusate exchange during long perfusions was provided by Liu [90] who used perfusate exchange in his successful 7 day storage experiments. Grundmann [91] also found that 96-hour preservation quality was improved by the use of a double volume of perfusate or by perfusate exchange. However, Grundmann's conclusions were based on comparisons with a control group of only 3 dogs. Cohen [92] was unable to demonstrate any production of ammonia during 8 days of perfusion and no benefit from perfusate exchange; the progressive alkalinity that occurred during perfusion was shown to be due to bicarbonate production.

Toxic damage from the perfusate

Certain perfusates have been shown to have toxic effects on kidneys as a result of the inadvertent inclusion of particular chemicals in their formulation. Collins [93] showed that the procaine included in the formulation of his flush fluids could be toxic, and Pegg [94] has commented how toxic materials, such as PVC plasticizers, may be washed out of perfusion circuit tubing. Dvorak [95] showed that the methyl-prednisolone addition to the perfusate that was thought to be essential by Woods [96] might in some circumstances be harmful. He showed that with over 2 g of methyl-prednisolone in 650 ml of perfusate (compared with 250 mg in 1 litre used by Woods) irreversible haemodynamic and structural changes were produced in the kidney after 20 hours of perfusion. There was necrosis of capillary loops, occlusion of Bowman's spaces, basement membrane thickening and endothelial cell damage.

Washout of essential substrates

The level of nucleotides remaining in the cell after storage was thought by Warnick [97] to be important in determining whether the cell would be able to re-synthesize ATP and recover after rewarming. Frequent changing of the perfusate or the use of a large volume of perfusate has the theoretical disadvantage that broken down adenine nucleotides may be washed out of the cells and so not be available for re-synthesis into ATP when the kidney is rewarmed.

Injury to nuclear DNA

Nuclear DNA is injured during cold storage of kidneys. Lazarus [98] showed that single stranded DNA breaks occurred within 16 hours in hypothermically stored mice kidneys, with the injury being inhibited a little by storage in Collins' or Sacks' solutions. This nuclear injury differed from that seen in warm injury when double stranded DNA breaks occurred.[99]

Mechanical injury to the vascular system

Perfusion storage methods can mechanically injury the vascular endothelium of the kidney, which leads to arterial thrombosis or fibrin deposition after reimplantation. Hill [100] noted that, in human kidneys, fibrin deposition in the glomerulus after reimplantation and postoperative function, correlated with the length of perfusion storage. He had taken biopsies at revascularisation from human kidneys preserved by perfusion or ice storage, and showed by electron microscopy that endothelial disruption only occurred in those kidneys that had been perfused. Biopsies taken one hour after revascularisation showed platelets and fibrin adherent to any areas of denuded vascular basement membrane. A different type of vascular damage was described by Sheil [101] who showed how a jet lesion could be produced distal to the cannula tied into the renal artery, leading to arterial thrombosis approximately 1 cm distal to the cannula site.

Post reimplantation injury

There is evidence that immunological mechanisms may injure hypothermically perfused kidneys after reimplantation if the perfusate contained specific antibody. Cross [102] described two pairs of human cadaver kidneys that were perfused simultaneously with cryoprecipitated plasma containing type specific HLA antibody to one of the pairs. Both these kidneys suffered early arterial thrombosis. Light [103] described similar hyperacute rejection following perfusion storage and showed that the cryoprecipitated plasma used contained cytotoxic IgM antibody. This potential danger of using cryoprecipitated plasma was demonstrated experimentally by Filo [104] who perfused dog kidneys for 24 hours with specifically sensitised cryoprecipitated dog plasma and found that he could induce glomerular and vascular lesions with capillary engorgement, endothelial swelling, infiltration by polymorphonuclear leucocytes and arterial thrombosis. Immunofluorescent microscopy demonstrated specific binding of IgG along endothelial surfaces, in glomeruli, and also in vessels. After reimplantation, complement fixation and tissue damage occurred in a similar pattern. There was some correlation between the severity of the histological damage and subsequent function of the kidneys.

Many workers have attempted to prevent kidneys rewarming during reimplantation but only Cohen has described using a system of active cooling.[105] Measurements of lysosomal enzyme release from kidneys subjected to sham anastomoses, when either in or out of the cooling system, demonstrated how sensitive kidneys were to rewarming after a period of cold storage, and confirmed the effectiveness of the cooling system in preventing enzyme release. A further factor in minimising injury at the reimplantation operations may have been that the kidneys were kept at 7 °C within the cooling coil, which was within a degree of the temperature used during perfusion storage, so that the kidneys were not subjected to the greater changes in temperature that would have occurred if ice cooling had been used.

Dempster[106] described using slow release of the vascular clamps at the end of kidney reimplantation operations to avoid injuring the kidney, but other workers have not mentioned whether or not they used this manoeuvre. After Cohen found vascular injury with intra renal bleeding after 3 days of perfusion storage,[107] a technique of slow revascularisation was used for all subsequent experiments, with the aim of giving the intra- renal vessels time to recover their tone sufficiently to prevent full systolic pressure being applied to the fragile glomerular vessels. The absence of gross vascular injury in his later perfusions may be attributable to the use of this manoeuvre.

References

  1. ↑ Wight J, Chilcott J, Holmes M, Brewer N (2003). "The clinical and cost-effectiveness of pulsatile machine perfusion versus cold storage of kidneys for transplantation retrieved from heart-beating and non-heart-beating donors". Health Technol Assess 7 (25): 1–94. PMID 14499050.
  2. ↑ Cohen GL: 8 day kidney preservation, Ch.M. thesis, Liverpool University: Online as http://ethos.bl.uk/OrderDetails.do?did=1&uin=uk.bl.ethos.535952 and on AMAZON with corrections and full logs as http://www.amazon.com/Day-Kidney-Preservation-Geoffrey-Cohen-ebook/dp/B00GD8G8HW
  3. ↑ Cohen GL, Johnson RWG: "Perfusate buffering for 8-day canine kidney storage", Proceedings of the European Society for Artificial Organs, vol.7 (1980), p.235-239.
  4. ↑ Cohen GL, Hunt L, Johnson RWG: "Octanoate toxicity in 5 day kidney preservation", Cryobiology, vol.20 (1983), p.731.
  5. ↑ Cohen GL, Burdett K, Johnson RWG: "Stimulation of oxygen consumption by oleic and octanoic acid during hypothermic kidney preservation", Cryobiology, vol.22 (1985), p.615-616.
  6. ↑ Cohen GL, Burdett K, Hunt L, Johnson RWG: "Uncoupling of oxidative phosphorylation by octanoic acid during 5-day hypothermic kidney preservation", Cryobiology, vol.21 (1984), p.699-700.
  7. ↑ Carrel A. La technique operatoire des anastomoses vasculaires et la transplantation des visceres. Lyon med 1902;98:859-864.
  8. ↑ Ullman E. Experimentalle Nierentransplantation. Wein klin Wochschr. 1902;15:281-282.
  9. ↑ 34. Fuhrman FA, Field J. The reversibility of the inhibition of rat brain and kidney metabolism by cold. Am J Physiol 1943;139:193-196.
  10. ↑ Carrel A, Lindbergh CA. The culture of whole organs. Science 1935;81:621-623.
  11. ↑ Bainbridge FA, Evans CL. The heart, lung, kidney preparation. J Physiol 1914;48:278-286.
  12. ↑ Owens JC, Prevedel AE, Swan H. Prolonged experimental occlusion of thoracic aorta during hypothermia. Arch Surg 1955;70:95-97.
  13. ↑ Bogardus GM, Schlosser RJ. The influence of temperature upon ischaemic renal damage. Surgery 1956;39:970-974.
  14. ↑ Moyer JH, Morris G, DeBakey ME. Hypothermia:I. Effect on renal hemodynamics and on excretion of water and electrolytes in dog and man. Ann Surg 1957;145:26-39.
  15. ↑ Stueber P, Kovacs S, Koletsky S, Persky L. Regional renal hypothermia. Surgery 1958;44:77-83.
  16. ↑ Schloerb PR, Waldorf RD, Welsh JS. The protective effect of kidney hypothermia on total renal ischaemia. Surg Gynecol Obstet 1959;109:561-565.
  17. ↑ Kisser JC, Farley HH, Mueller GF, Strobel CJ, Hitchcock CR. Successful renal autografts in the dog after seven hour selective kidney refrigeration. Surg Forum 1960;11:26-28.
  18. ↑ Lapchinsky AG. Recent results of experimental transplantation of preserved limbs and kidneys and possible use of this technique in clinical practice. Ann N Y Aced Sci 1960;87:539-569.
  19. ↑ Humphries AL, Russell R, Ostafin J, Goodrich SM, Moretz WH. Successful reimplantation of Dog kidney after 24-hour storage. Surgical Forum 1962;13:380-382.
  20. ↑ Humphries AL, Russell R, Ostafin J, Goodrich SM, Moretz WH. Successful reimplantation of Dog kidney after 24-hour storage. Surgical Forum 1962;13:380-382.
  21. ↑ Calne RY, Pegg DE, Pryse-Davies J, Leigh Brown F. Renal preservation by ice cooling. Br Med J 1963;2:651-655.
  22. ↑ Humphries AL, Moretz WH, Peirce EC. Twenty-four hour kidney storage with report of a successful canine autotransplant after total nephrectomy. Surgery 1964;55:524-530.
  23. ↑ Manax WG, Block JH, Eyal Z, Lyons GW, Lillehei RC. Hypothermia and hyperbaria. JAMA 1965;192:755-759.
  24. ↑ Belzer FO, Ashby BS, Dunphy JE. 24-hour and 72-hour preservation of canine kidneys. Lancet 1967;2:536-539.
  25. ↑ Belzer FO, Ashby BS, Huang JS, Dunphy JE. Etiology of rising perfusion pressure in isolated organ perfusion. Ann Surg 1968;168:382-391.
  26. ↑ Lotke PA. Lysosome stabilising agents for hypothermic kidney preservation. Nature 1966;212:512-513.
  27. ↑ Suomalainen P. Production of artificial hibernation. Nature 1938;142:1157.
  28. ↑ Kamiyama TM, Webb WR, Ecker RR. Preservation of the anoxic heart with a metabolic inhibitor and hypothermia. Arch Surg 1970;100:596-599.
  29. ↑ Belzer FO, Kountz SL. Preservation and transplantation of human cadaver kidneys: a two year experience. Ann Surg 1970;172:394-404.
  30. ↑ Humphries AL, Russell R, Stoddard LD, Moretz WH. Successful five-day kidney preservation. Invest Urol 1968;5:609-617.
  31. ↑ Collins GM, Bravo-Shugarman M, Terasaki PI. Kidney preservation for transportation. Lancet 1969;2:1219-1222.
  32. ↑ Keller R, Swinney J, Taylor RMR, Uldall PR. The problem of renal preservation. Br J Urol 1966;38:653-656.
  33. ↑ Duff RS, Ginsberg J. Some peripheral vascular effects of intra-arterial dibenyline in man. Clin Sci 1957;16:187-196.
  34. ↑ Rangel DM, Bruckner WL, Byfield JE, Dinbar JE, Yakeishi Y, Stevens GH, Fonkalsrud EW. Enzymatic evaluation of hepatic preservation using cell-stabilising drugs. Surg Gynecol Obstet 1969;129:963-972.
  35. ↑ Liu WP, Humphries AL, Stoddard LD, Moretz WH. 48-hour kidney storage. Letter. Lancet 1970;2:423.
  36. ↑ Woods JE, Cooperman AM, Holley KE. Problems in 48- to 72-hour preservation of canine kidneys. Arch Surg 1970;101:605-609.
  37. ↑ Woods JE. Successful three- to seven day preservation of canine kidneys. Arch Surg 1971;102:614-616.
  38. ↑ Johnson RWG, Anderson M, Flear CTG, Murray SGH, Taylor RMR, Swinney J. Evaluation of a new perfusion solution for kidney preservation. Transplantation 1972;13:270-275.
  39. ↑ Claes G, Aurell M, Blohme I, Petterson S. Experimental and clinical results of continuous hypothermic albumin perfusion. Proc Eur Dial Transplant Assoc 1972;9:484-490.
  40. ↑ Murray R, Diefenbach WCL. Effect of heat on the agent of homologous serum hepatitis. Proc Soc Exp Biol Med 1953;84:230-231.
  41. ↑ Hink JH, Pappenhagen AR, Lundblad J, Johnson FF. Plasma Protein Fraction (Human): Physical and Clinical Properties after Storage for 7-8 Years. Vox Sang 1970;18:527-541.
  42. ↑ Horsburgh T. Possible role of free fatty acids in kidney preservation media. Nature (New Biol) 1973;242:122-123.
  43. ↑ Johnson RWG, Anderson M, Flear CTG, Murray SGH, Taylor RMR, Swinney J. Evaluation of a new perfusion solution for kidney preservation. Transplantation 1972;13:270-275.
  44. ↑ Johnson RWG. Studies in renal preservation. Newcastle, England: University of Newcastle, 1973. 94pp. M. S. Thesis.
  45. ↑ Claes G, Aurell M, Blohme I, Petterson S. Experimental and clinical results of continuous hypothermic albumin perfusion. Proc Eur Dial Transplant Assoc 1972;9:484-490.
  46. ↑ Liu WP, Humphries AL, Russell R, Stoddard LD, Garcia LA, Serkes KD. Three- and seven-day perfusion of dog kidneys with human plasma protein fraction IV-4. Surgical Forum 1973;24:316-318.
  47. ↑ Humphries AL, Garcia LA, Serkes KD. Perfusates for long-term preservation by continuous perfusion. Transplantation Proceedings 1974;6:249-253.
  48. ↑ Joyce M, Proctor E. Hypothermic perfusion-preservation of dog kidneys for 48-72 hours without plasma derivatives or membrane oxygenation. Transplantation 1974;18:548-550.
  49. ↑ Sacks SA, Petritsch PH, Kaufman JJ. Canine kidney preservation using a new perfusate. Lancet 1973;1:1024-1028.
  50. ↑ Ross H, Marshall VC, Escott ML. 72-hr canine kidney preservation without continuous perfusion. Transplantation 1976;21:498-501.
  51. ↑ Collins GM, Halasz NA. Simplified 72-hr kidney storage. Surgical Forum 1974;25:275-277.
  52. ↑ Collins GM, Halasz NA. The role of pulsatile flow in kidney preservation. Transplantation 1973;16:378-379.
  53. ↑ Collins GM, Halasz NA. Simplified 72-hr kidney storage. Surgical Forum 1974;25:275-277.
  54. ↑ Grundmann R, Rabb M, Meusel E, Kirchhoff R, Pichlmaier H. Analysis of the optimum perfusion pressure and flow rate of the renal vascular resistance and oxygen consumption in the hypothermic perfused kidney. Surgery 1975;77:451-461.
  55. ↑ Cohen GL: 8 day kidney preservation, Ch.M. thesis, Liverpool University: Online as http://ethos.bl.uk/OrderDetails.do?did=1&uin=uk.bl.ethos.535952 and on AMAZON with corrections and full logs as http://www.amazon.com/Day-Kidney-Preservation-Geoffrey-Cohen-ebook/dp/B00GD8G8HW
  56. ↑ Cohen GL, Burdett K, Johnson RWG: "Stimulation of oxygen consumption by oleic and octanoic acid during hypothermic kidney preservation", Cryobiology, vol.22 (1985), p.615-616.
  57. ↑ 75. Mackay B, Moloney PJ, Rix DB. The use of electron microscopy in renal preservation and perfusion. In: Norman JC, ed. Organ perfusion and preservation. New York: Appleton Century Crofts,1968:697-714.
  58. ↑ Woods JE. Successful three- to seven day preservation of canine kidneys. Arch Surg 1971;102:614-616.
  59. ↑ Woods JE, Fleisher GA, Hirsche BL. Five-day perfusion of canine kidneys: A postulated effect of steroids. Transplantation Proceedings 1974;6:255-260.
  60. ↑ Liu WP, Humphries AL, Russell R, Stoddard LD, Garcia LA, Serkes KD. Three- and seven-day perfusion of dog kidneys with human plasma protein fraction IV-4. Surgical Forum 1973;24:316-318.
  61. ↑ Hill GS, Light JA, Perloff LJ. Perfusion-related injury in renal transplantation. Surgery 1976;79:440-447.
  62. ↑ Kastagir BK, Kabb K, Leonards JR. Ultrastructure in the canine kidney preserved for 24 hours. Trans Am Soc Artific Intern Organs 1969;15:214-218.
  63. ↑ Scott DF, Morley AR, Swinney J. Canine renal preservation following hypothermic perfusion and subsequent function. Brit J Surg 1969;56:688-691.
  64. ↑ Pederson FB, Hrynczuk JR, Scheibel JH, Sorensen BL. Urine production and metabolism of glucose and lactate acid in the kidney during 36 hours of cooling and perfusion with diluted plasma. Scand J Urol Nephrol 1973;7:68-73.
  65. ↑ Woods JE, Fleisher GA, Hirsche BL. Five-day perfusion of canine kidneys: A postulated effect of steroids. Transplantation Proceedings 1974;6:255-260.
  66. ↑ Cohen GL: 8 day kidney preservation, Ch.M. thesis, Liverpool University: Online as http://ethos.bl.uk/OrderDetails.do?did=1&uin=uk.bl.ethos.535952 and on AMAZON with corrections and full logs as http://www.amazon.com/Day-Kidney-Preservation-Geoffrey-Cohen-ebook/dp/B00GD8G8HW
  67. ↑ McLoughlin GA, Sells RA, Tyrrell I. An evaluation of kidney preservation techniques. Br J Surg 1974;61:406-409.
  68. ↑ Glynn IM. Membrane adenosine triphosphatase and cation transport. Br Med Bull 1968;24(2):165-169.
  69. ↑ Levy MN. Oxygen consumption and blood flow in the hypothermic, perfused kidney. Am J Physiol 1959;197:1111-1114.
  70. ↑ Martin DR, Scott DF, Downes GL, Belzer FO. Primary cause of unsuccessful liver and heart preservation: Cold sensitivity of the ATPase system. Ann Surg 1972;175:111-114.
  71. ↑ Belzer FO, Hoffman R, Huang J, Downes G. Endothelial damage in perfused dog kidney and cold sensitivity of vascular Na-K-ATPase. Cryobiology 1972; 9:457-460 .
  72. ↑ Willis JS. Characteristics of ion transport in kidney cortex of mammalian hibernators. J Gen Physiol 1966;49:1221-1239.
  73. ↑ Francavilla A, Brown TH, Fiore R, Cascardo S, Taylor P, Groth CG. Preservation of organs for transplantation. Evidence of detrimental effect of rapid cooling. Europ Surg Res 1973;5:384-389.
  74. ↑ Bergstrom J, Collste H, Groth C, Hultman E, Melin B. Water, electrolyte and metabolic content in cortical tissue from dog kidneys preserved by hypothermia. Proc Eur Dialysis Transplant Ass 1971;8:313-320.
  75. ↑ Warnick CT, Lazarus HM. The maintenance of adenine nucleotide levels during kidney storage in intracellular solutions. Proc Soc Exp Biol Med 1979;160:453-457.
  76. ↑ Pegg DE, Wusteman MC, Foreman J. Metabolism of normal and ischaemically injured rabbit kidneys during perfusion for 48 hrs at 10°C. Transplantation 1981;32:437-443.
  77. ↑ Lannon SG, Tukaram KT, Oliver JA, MacKinnon KJ, Dossetor JB. Preservation of kidneys assessed by a biochemical parameter. Surg Gynecol Obstet 1967;124:999-1004.
  78. ↑ Pettersson S, Claes G, Schersten T. Fatty acid and glucose utilisation during continuous perfusion of dog kidney. Europ Surg Res 1974;6:79-94.
  79. ↑ Cohen GL: 8 day kidney preservation, Ch.M. thesis, Liverpool University: Online as http://ethos.bl.uk/OrderDetails.do?did=1&uin=uk.bl.ethos.535952 and on AMAZON with corrections and full logs as http://www.amazon.com/Day-Kidney-Preservation-Geoffrey-Cohen-ebook/dp/B00GD8G8HW
  80. ↑ Pettersson S, Claes G, Schersten T. Fatty acid and glucose utilisation during continuous perfusion of dog kidney. Europ Surg Res 1974;6:79-94.
  81. ↑ Cohen GL: 8 day kidney preservation, Ch.M. thesis, Liverpool University: Online as http://ethos.bl.uk/OrderDetails.do?did=1&uin=uk.bl.ethos.535952 and on AMAZON with corrections and full logs as http://www.amazon.com/Day-Kidney-Preservation-Geoffrey-Cohen-ebook/dp/B00GD8G8HW
  82. ↑ Lee JB, Vance VK, Cahill GF. Metabolism of C14-labeled substrates by rabbit kidney cortex and medulla. Amer J Physiol 1962;203:27-36.
  83. ↑ Abodeely DA, Lee JB. Fuel of respiration of renal medulla. Am J Physiol 1971;220:1693-1700.
  84. ↑ Horsburgh T. Possible role of free fatty acids in kidney preservation media. Nature (New Biol) 1973;242:122-123.
  85. ↑ Pettersson S, Claes G, Schersten T. Fatty acid and glucose utilisation during continuous perfusion of dog kidney. Europ Surg Res 1974;6:79-94.
  86. ↑ Huang JS, Downes GL, Belzer FO. Utilisation of fatty acids in perfused hypothermic dog kidney. J Lipid Res 1971;12:622-627.
  87. ↑ Huang JS, Downes GL, Childress GL, Felts JM, Belzer FO. Oxidation of C14 -labelled substrates by dog kidney cortex at 10`C and 38`C. Cryobiology 1974;11:387-394.
  88. ↑ Lee KY. Loss of lipid to plastic tubing. J Lipid Res 1971;12:635-636.
  89. ↑ Abouna GM, Lim F, Cook JS, Grubb W, Craig SS, Seibel HR, Hume DM. Three-day canine kidney preservation. Surgery 1972;71:436-444.
  90. ↑ Liu WP, Humphries AL, Russell R, Stoddard LD, Garcia LA, Serkes KD. Three- and seven-day perfusion of dog kidneys with human plasma protein fraction IV-4. Surgical Forum 1973;24:316-318.
  91. ↑ Grundmann R, Berr F, Pitschi H, Kirchhoff R, Pichlmaier H. Ninety-six-hour preservation of canine kidneys. Transplantation 1974;17:290-305.
  92. ↑ Cohen GL: 8 day kidney preservation, Ch.M. thesis, Liverpool University: Online as http://ethos.bl.uk/OrderDetails.do?did=1&uin=uk.bl.ethos.535952 and on AMAZON with corrections and full logs as http://www.amazon.com/Day-Kidney-Preservation-Geoffrey-Cohen-ebook/dp/B00GD8G8HW
  93. ↑ Collins GM, Halasz NA. Forty-eight hour ice storage of kidneys. Importance of cation content. Surgery 1976;79:432-435.
  94. ↑ Pegg DE, Fuller BJ, Foreman J, Green CJ. The choice of plastic tubing for organ perfusion experiments. Cryobiology 1973;8:569-571.
  95. ↑ Dvorak KJ, Braun WE, Magnusson MO, Stowe NT, Banowsky LHW. Effect of high doses of methylprednisolone on the isolated perfused canine kidney. Transplantation 1976;21:149-157.
  96. ↑ Woods JE, Fleisher GA, Hirsche BL. Five-day perfusion of canine kidneys: A postulated effect of steroids. Transplantation Proceedings 1974;6:255-260.
  97. ↑ Warnick CT, Lazarus HM. The maintenance of adenine nucleotide levels during kidney storage in intracellular solutions. Proc Soc Exp Biol Med 1979;160:453-457.
  98. ↑ Lazarus HM, Warnick CT, Hopfenbeck A. DNA strand breakage after kidney storage. Cryobiology 1982;19:129-135.
  99. ↑ Lazarus HM, Hopfenbeck A. DNA degradation during storage. Experientia 1974;30:1410-1411.
  100. ↑ Hill GS, Light JA, Perloff LJ. Perfusion-related injury in renal transplantation. Surgery 1976;79:440-447.
  101. ↑ Sheil AGR, Drummond JM, Boulas J. Vascular thrombosis in machine-perfused renal allografts. Transplantation 1975;2:178-179.
  102. ↑ Cross DE, Whittier FC, Cuppage FE, Crouch T, Manuel EL, Grantham JJ. Hyperacute rejection of renal allografts following pulsatile perfusion with a perfusate containing antibody. Transplantation 1974;17:626-629.
  103. ↑ Light JA, Annable C, Perloff LJ, Sulkin MD, Hill GS, Etheredge EE, Spees EKJr. Immune injury from organ preservation. Transplantation 1975;19:511:516.
  104. ↑ Filo RS, Dickson LG, Suba EA, Sell KW. Immunologic injury induced by ex vivo perfusion of canine renal autografts. Surgery 1974;76:88-100.
  105. ↑ Cohen GL: 8 day kidney preservation, Ch.M. thesis, Liverpool University: Online as http://ethos.bl.uk/OrderDetails.do?did=1&uin=uk.bl.ethos.535952 and on AMAZON with corrections and full logs as http://www.amazon.com/Day-Kidney-Preservation-Geoffrey-Cohen-ebook/dp/B00GD8G8HW
  106. ↑ Dempster WJ, Kountz SL, Javanovic M. Simple kidney-storage technique. Br Med J 1964;1:407-410.
  107. ↑ Cohen GL: 8 day kidney preservation, Ch.M. thesis, Liverpool University: Online as http://ethos.bl.uk/OrderDetails.do?did=1&uin=uk.bl.ethos.535952 and on AMAZON with corrections and full logs as http://www.amazon.com/Day-Kidney-Preservation-Geoffrey-Cohen-ebook/dp/B00GD8G8HW
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