CA1270199A - Preservation of living tissue - Google Patents
Preservation of living tissueInfo
- Publication number
- CA1270199A CA1270199A CA000516289A CA516289A CA1270199A CA 1270199 A CA1270199 A CA 1270199A CA 000516289 A CA000516289 A CA 000516289A CA 516289 A CA516289 A CA 516289A CA 1270199 A CA1270199 A CA 1270199A
- Authority
- CA
- Canada
- Prior art keywords
- perfusion
- pharmaceutical composition
- physiologically acceptable
- preservation
- acetoacetate
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N1/00—Preservation of bodies of humans or animals, or parts thereof
- A01N1/02—Preservation of living parts
- A01N1/0205—Chemical aspects
- A01N1/021—Preservation or perfusion media, liquids, solids or gases used in the preservation of cells, tissue, organs or bodily fluids
- A01N1/0221—Freeze-process protecting agents, i.e. substances protecting cells from effects of the physical process, e.g. cryoprotectants, osmolarity regulators like oncotic agents
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N1/00—Preservation of bodies of humans or animals, or parts thereof
- A01N1/02—Preservation of living parts
Abstract
Abstract Preservation of living tissue To preserve living tissue during operations on or transplantations of organs, acetoacetate is added to the perfusion solutions in the presence of pyruvate.
The acetoacetate has a protective effect, particularly on the heart, in the event of anoxia or ischaemia.
The acetoacetate has a protective effect, particularly on the heart, in the event of anoxia or ischaemia.
Description
~L2~
1 This invention relates to the preservation o living tissue in the absence of oxygenation or in the event ofin-sufficient oxygenation by the blood.
Under normal oxygenation conditions, r'eduction of the oxygen by the mitochondrial respiratory system supplies most of the energy emanating from the catabolism of the fatty acids and glucides in the form of adenosine triphosphate (ATP).
- The reduction in the ATP and creatinine phosphate content of tissues which occurs in pexio'ds of non-oxygenation (anoxia)or insufficientirrigation (ischaemia) by the blood promotes the development of irreversible cell changes during those periods and during reoxygenation of the tissues.
When the tissue is not irrigated and deprived of oxygen, the fermentation of glucose into lactate does supply some energy, but is accompanied by acidification of the cytoplasm of the'cell due to the accumulation of lactate. This intra~
cellular acidification impedes the metabolism and compromises the resumption of function of the tissue when irrigation and oxygenation resume.
The hypothesis has been put forward that, in certain animals, the metabolization under anaerobic conditions of aspartate and glutamate into succinate was linked to the non-oxidative-phosphorylation of adenosine diphosphate (ADP) occurring inside the mitochondria (Hochachka, P., 25 Owen, T.G., Amer. Zool. 13: 543-555, 1973).
On the other hand, the effect of intravenous infusion of glycerol monoacetoacetate as a non-protein energy source in burnt rats has been described and it has been shown that `this compound can replace glucose as a source of energy during parenteral nutrition (Maiz, A., Moldawer, L.L., Bistrian, B.R., Biochem. J., 1985, 226/1, 43-50).
Applicants have found that the addition of acetoacetate to a solution for perfusion of the heart under conditions of 7~
1 anoxia afforded protection against the functional changes resulting from the anoxia. This protective e~fect probably resulted from an anaerobic production of energy associated with the non-oxidative phosphorylation of ADP occurring in S the mitochondria where the reduction of acetoacetate to ~-hydroxybutyrate was coupled with the oxidation o~ other intra-cellular substrates into succinate. An effect such as this can also have a beneficial role in the preservation of other tissues than the heart, for example the kidneys, the liver or the eyes in the event of anoxia and ischaemia.
Accordingly, the invention relates to the use of aceto-acetic acid or one of its physiologically acceptable salts or esters for obtaining a pharmaceutical composition intended for the preservation of living tissues in the absence of oxygenation or in the event of insufficient ox~genation by the blood.
Physiologically acceptable salts or esters are under-stood to be the salts or esters which are normally encountered in perfusion or cardioplegic solutions. It is preferred to use sodium salts in an effective quantity for ~h~ desired protective effect.
The pharmaceutical composition advantageously also contains pyruvic acid or one of its physiologically acceptable salts or esters, preferably sodium pyruvate. It may also contain an energy-producing agent, for example glucose.
The pharmaceutical composition is advantageously formulated as a sterile isotonic or slightly hypertonic, physiological aqueous solution, for example a perfusion or cardioplegic solution o~ the type commonly used in operations o~ or transplantations of organs.
It is preferably used in situations where the organs are exposed to prolonged periods of anoxia or ischaemia, for example during cardiac infarction or transplantation.
Although the protective e4fect has been demonstrated in the case of the heart, there is no reason to assume that it . :. .
.: :
:
' ~27C~lg~
1 would not be developed during operations on or transplantations of other organs, for example the eyes, the liver or the kidneys.
The invention is illustrated by the ~ollowing Example which is preceded by a description of the method used for the various measurements of the cardiac function.
Perfusion system The perfusion system will be better understood from the accompanying drawings, wherein:
Figure 1 is a schematic view of the perfusion system.
Figure 2 shows a particular diagram of the perfusion system used solely during the anaerobic period.
In Figure 1, the heart 1 is canalized by the aorta 2, the pulmonary veins 3 and the pulmonary artery 4. It is connected to the perfusion circuit by a cannula 5 of which one end is introduced into the aorta 2. The cannula S is itself connected at its other end to a peristaltic pump 6 (pulsed output) via thermostatically controlled double-walled reservoirs 7. Cannulas 8 and 9 respectively connect the pulmonary veins 3 to thermostatically controlled double-walled reservoirs lO,ll and the pulmonary artery 4 to a thermostatically controlled double-walled chamber 12 surrounding the heart. A cellulose acetate filter 13 (pore diameter 0.8 ~m) placed between the reservoirs ll and the pump 6 permanently clarifies the perfusion solution. The reservoirs lOjll are provided with two circuits 14 for respectively supplying the perfusion liquid by bubbling with an oxygenated gas mixture (95~:O2-5~:CO2) and a non-- oxygenated gas mixture (95%:N2-5~:CO2). ~alves 15 provide for immediate changeover from the retrograde perfusion technique, in which the heart l is perfused through the aorta 2 and does not expel liquid, to the anterograde or so-called "working heart" perfusion techni~ue in which the heart is perfused through the pu~nary veins 3 and develops an aortic flow. In both techniques, it is possible to measure the .
9~
coronary flow of the liquid which flows freely through the pulmonary artery 4 to the thermostatically controlled chamber 12 and is collected from there in a graduated cylinder 16.
The pump 6 circulates the p~rfusion liquid and regulates the basic aortic pressure (post-charge). The filling pressure of the left ventricle (pre-charge) is reyulated by vertical displacement of the reservoir lO connected to canula 8.
In 17, the aortic pressure is measured by a pressure trans-ductor (the pressure being calihrated by a mercur~ manometer 18), and the aortic flow is measured by an electromagnetic flowmeter with the aid of an intra-aortic probe.
In Figure 2, an additional circuit segment connected to the non-oxygenated circuit comprises a pump 19 of constant 15 and adjustable output by which the perfusion liquid can be circulated by the retrograde aortic route. The substances to be tested are introduced into the perfusion liquid at the level of the aorta by a miniature metering pump 20 of constant and adjustable output.
20 Perfusion method and measurements The heart is taken from adult male Sprague-Dawley rats which have a body weight of from 250 to 320 g and which have been fed on a standard regime. The animals are mildly anaesthe-tized with ether and then decapitated. After excision, the 25 heart is rapidly immersed in physiological salt solution cooled to 4C which causes rapid cessation of the contractile acti-vity. The perfusion period is divided into three phases.
Phase 1: aerobic stabilization period The heart is rapidly connected to the per~us~on system 30 through the aorta and then perfused by the retrograde kech-nique at a hydrostatic pressure of 7.8 kPa (60 mm Hg) which permits rinsing of the residual blood and resumption of the spontaneous beat. The pulmorary veins and the pulmonary artery are then connected up. The total duration of these 35 two operations is 5 minutes. Perfusion is then changed over by means of the valves 15 to the anterograde technique , .. . ~.
.
: .
~L2'~ 9 1 using a liquid gassed with the oxygenated mixture which perfuses through the left atrium with a pre-charge of 1.6 kPa (160 mm H2O)and a post-charge of 7.8 kPa (60 mm Hg).
After a 15-minute stabilization period, the cardiac output (ml/min.) is measured, the cardiac output being the sum of the aortic andcoronary outputs (liquid issuing from the chamber 12 coming from the pulmonary artery and losses through the apex of the heart).
Phase 2: anaerobic pe iod During this period which lasts 30 or 45 minutes, the heart is perfused through the aorta at a constant xate of 15 ml/min. with a perfusion liquid gassed wi-th the non-oxygenated mixture. The solutions of substances to be treated are directly injected at the level of the aorta by the miniature pump 20 at a rate of 0.I5 ml/min., the final molar concentration of these substance~ being 5 mM. After a few minutes of the anaerobic period, the contractile function of the heart stops completely.
Phase 3: aerobic recoverY period The heart is again perfused through the left atrium (anterograde technique) with a perfusion liquid gassed with the oxygenated mixture. The cardiac output and the aortic pressure are measured 15 and 30 minutes after reoxygenation of the perfusion liquid. They are expressed as a percentage 25 of the values obtained before the anaerobic period.
Perfusion liquids The stock per~usion liquid used is a bicarbonate buffer solution of the Krebs-Henseleit type brought to the temper-ature of 37C and consisting of: 120 mM NaCl, 5 mM KCl, 30 2.5 mM CaC12, 25 mM NaHCO3, 1.2 mM KH2PO4, 1-2 mM MgSO4 and 10 mM sodium pyruvate or sodium lactate.
The substances to be tested were prepared on the day of the test and their p~ adjusted to 7.4 with NaOH. They were only added to the stock perfusion liquid during the 35 anaerobic phase.
~ , . , ..~
, ~C)~39 45 hearts were perfused with a stock perfusion liquid containing sodium pyruvate and 50 hearts with a stock per-fusion liquid containing sodium lactate, after which the cardiac function parameters were measured at the end of phase 1 (aerobic period). The results obtained are shown in Table 1 below:
Stock continuous perfusion liquid conta.ining Pyruvate Lactate Weight of wet hearts (g) 1.46 + 0.03 1.39 + 0.03 15 OutputS (ml/min.) Aortic 19.1 + 1.14 22.9 ~ 1.1 Coronary 30.2 + 1.3 27.3 + 1.01 Cardiac 49.3 + 1.46 50.2 + 1.36 ~ .
Systolic aortic pressure (kPa) 13.78 + 0.25 14.25 ~ 0.23 After an anaerobic period of 30 or 45 minutes (phase 2), during which some of the hearts were perfused with the solutions of substances indicated in Table 2 below, the functional recovery (phase 3) varied according to the nature of the substances supplied to the hearts during the anaerobic phase as shown in Table 2 below which indicates the proportion of hearts recovering a cardiac output after the anaerobic period.
.
~:
.
~7 [)~
Propor~ion of hearts Substrates recovering a cardiac output after an anaerobic ~eriod of Stock continuous Solutions of sub-perfusion liquid stances to be tes- 30 mins. 45 mins.
containing ted perfused dur-ing the anaerobic period Lactate (control) 1/3 Lactate Aspartate 4/4 0/10 Aspartate + glutam-ate + pyruvate* 1/3 -Pyruvate (control) 5/5 1/5 Acetoacetate 10/10 9/10 Pyruvate Acetoacetate +
glutamate* 4/4 0/4 ~-hydroxybutyrate 2/3 0/3 Note: The aspartate, the glutamate, the pyruvate and the acetoacetate are in the form of the sodium salt.
* When there are several perfused subs~ances (during the anaerobic period), they are success~vely introduced so . that their final individual concentration is 5 mM.
Remarks:
The majority of hearts in the control group receiving the lactate (stock perfusion liquid~ did not recover measurable functions after reoxygenation. The addition of aspartate to ~he stock perfusion liquid provided for functional recovery of all the hearts examined after an anaerobic per:iod of 30 minutes. The extra addi~ion of : ., ....
,~ ~
:. . . :-~.. ' ' " ~ ' - ::
,.:'' ~... .
~7~)199 1 glutamate appeared to interfere with the effect of the aspartate. In none of these groups was recovery observed after an anaerobic period of 45 minutes.
After an anaerobic period of 45 minutes in the presence of pyruvate (stock perfusion liquid), the proportion of hearts recovering a measurable output was significantly higher in the group receiving the acetoacetate than in the control group.
After an anaerobic period of 30 minutes, 95% of the hearts examined had recovered a measurable function. However, better recovery of the cardiac contractility was already noticeable in the group receiving the acetoacetate. Thus, the aortic pressure was 69 ~3% of its value before the anaerobic period and the cardiac output 34 +7~ of its value before the anaerobic period for the control group. For the group receiving the acetoacetate, the aortic pressure was 7~ + 3% of its value before the anaerobic period and the cardiac output 52 ~7% of its value before the anaerobic period.
The improvement in the tolerance by the heart of the anaerobic state produced by the acetoacetate was not enhanced but rather impaired by the addition of glutamate. In addition, the perfusion of ~-hydroxybutyrate did not have a protective effect.
~, : . ' , , - , , .
.~ -.
:
, , .: ,:
1 This invention relates to the preservation o living tissue in the absence of oxygenation or in the event ofin-sufficient oxygenation by the blood.
Under normal oxygenation conditions, r'eduction of the oxygen by the mitochondrial respiratory system supplies most of the energy emanating from the catabolism of the fatty acids and glucides in the form of adenosine triphosphate (ATP).
- The reduction in the ATP and creatinine phosphate content of tissues which occurs in pexio'ds of non-oxygenation (anoxia)or insufficientirrigation (ischaemia) by the blood promotes the development of irreversible cell changes during those periods and during reoxygenation of the tissues.
When the tissue is not irrigated and deprived of oxygen, the fermentation of glucose into lactate does supply some energy, but is accompanied by acidification of the cytoplasm of the'cell due to the accumulation of lactate. This intra~
cellular acidification impedes the metabolism and compromises the resumption of function of the tissue when irrigation and oxygenation resume.
The hypothesis has been put forward that, in certain animals, the metabolization under anaerobic conditions of aspartate and glutamate into succinate was linked to the non-oxidative-phosphorylation of adenosine diphosphate (ADP) occurring inside the mitochondria (Hochachka, P., 25 Owen, T.G., Amer. Zool. 13: 543-555, 1973).
On the other hand, the effect of intravenous infusion of glycerol monoacetoacetate as a non-protein energy source in burnt rats has been described and it has been shown that `this compound can replace glucose as a source of energy during parenteral nutrition (Maiz, A., Moldawer, L.L., Bistrian, B.R., Biochem. J., 1985, 226/1, 43-50).
Applicants have found that the addition of acetoacetate to a solution for perfusion of the heart under conditions of 7~
1 anoxia afforded protection against the functional changes resulting from the anoxia. This protective e~fect probably resulted from an anaerobic production of energy associated with the non-oxidative phosphorylation of ADP occurring in S the mitochondria where the reduction of acetoacetate to ~-hydroxybutyrate was coupled with the oxidation o~ other intra-cellular substrates into succinate. An effect such as this can also have a beneficial role in the preservation of other tissues than the heart, for example the kidneys, the liver or the eyes in the event of anoxia and ischaemia.
Accordingly, the invention relates to the use of aceto-acetic acid or one of its physiologically acceptable salts or esters for obtaining a pharmaceutical composition intended for the preservation of living tissues in the absence of oxygenation or in the event of insufficient ox~genation by the blood.
Physiologically acceptable salts or esters are under-stood to be the salts or esters which are normally encountered in perfusion or cardioplegic solutions. It is preferred to use sodium salts in an effective quantity for ~h~ desired protective effect.
The pharmaceutical composition advantageously also contains pyruvic acid or one of its physiologically acceptable salts or esters, preferably sodium pyruvate. It may also contain an energy-producing agent, for example glucose.
The pharmaceutical composition is advantageously formulated as a sterile isotonic or slightly hypertonic, physiological aqueous solution, for example a perfusion or cardioplegic solution o~ the type commonly used in operations o~ or transplantations of organs.
It is preferably used in situations where the organs are exposed to prolonged periods of anoxia or ischaemia, for example during cardiac infarction or transplantation.
Although the protective e4fect has been demonstrated in the case of the heart, there is no reason to assume that it . :. .
.: :
:
' ~27C~lg~
1 would not be developed during operations on or transplantations of other organs, for example the eyes, the liver or the kidneys.
The invention is illustrated by the ~ollowing Example which is preceded by a description of the method used for the various measurements of the cardiac function.
Perfusion system The perfusion system will be better understood from the accompanying drawings, wherein:
Figure 1 is a schematic view of the perfusion system.
Figure 2 shows a particular diagram of the perfusion system used solely during the anaerobic period.
In Figure 1, the heart 1 is canalized by the aorta 2, the pulmonary veins 3 and the pulmonary artery 4. It is connected to the perfusion circuit by a cannula 5 of which one end is introduced into the aorta 2. The cannula S is itself connected at its other end to a peristaltic pump 6 (pulsed output) via thermostatically controlled double-walled reservoirs 7. Cannulas 8 and 9 respectively connect the pulmonary veins 3 to thermostatically controlled double-walled reservoirs lO,ll and the pulmonary artery 4 to a thermostatically controlled double-walled chamber 12 surrounding the heart. A cellulose acetate filter 13 (pore diameter 0.8 ~m) placed between the reservoirs ll and the pump 6 permanently clarifies the perfusion solution. The reservoirs lOjll are provided with two circuits 14 for respectively supplying the perfusion liquid by bubbling with an oxygenated gas mixture (95~:O2-5~:CO2) and a non-- oxygenated gas mixture (95%:N2-5~:CO2). ~alves 15 provide for immediate changeover from the retrograde perfusion technique, in which the heart l is perfused through the aorta 2 and does not expel liquid, to the anterograde or so-called "working heart" perfusion techni~ue in which the heart is perfused through the pu~nary veins 3 and develops an aortic flow. In both techniques, it is possible to measure the .
9~
coronary flow of the liquid which flows freely through the pulmonary artery 4 to the thermostatically controlled chamber 12 and is collected from there in a graduated cylinder 16.
The pump 6 circulates the p~rfusion liquid and regulates the basic aortic pressure (post-charge). The filling pressure of the left ventricle (pre-charge) is reyulated by vertical displacement of the reservoir lO connected to canula 8.
In 17, the aortic pressure is measured by a pressure trans-ductor (the pressure being calihrated by a mercur~ manometer 18), and the aortic flow is measured by an electromagnetic flowmeter with the aid of an intra-aortic probe.
In Figure 2, an additional circuit segment connected to the non-oxygenated circuit comprises a pump 19 of constant 15 and adjustable output by which the perfusion liquid can be circulated by the retrograde aortic route. The substances to be tested are introduced into the perfusion liquid at the level of the aorta by a miniature metering pump 20 of constant and adjustable output.
20 Perfusion method and measurements The heart is taken from adult male Sprague-Dawley rats which have a body weight of from 250 to 320 g and which have been fed on a standard regime. The animals are mildly anaesthe-tized with ether and then decapitated. After excision, the 25 heart is rapidly immersed in physiological salt solution cooled to 4C which causes rapid cessation of the contractile acti-vity. The perfusion period is divided into three phases.
Phase 1: aerobic stabilization period The heart is rapidly connected to the per~us~on system 30 through the aorta and then perfused by the retrograde kech-nique at a hydrostatic pressure of 7.8 kPa (60 mm Hg) which permits rinsing of the residual blood and resumption of the spontaneous beat. The pulmorary veins and the pulmonary artery are then connected up. The total duration of these 35 two operations is 5 minutes. Perfusion is then changed over by means of the valves 15 to the anterograde technique , .. . ~.
.
: .
~L2'~ 9 1 using a liquid gassed with the oxygenated mixture which perfuses through the left atrium with a pre-charge of 1.6 kPa (160 mm H2O)and a post-charge of 7.8 kPa (60 mm Hg).
After a 15-minute stabilization period, the cardiac output (ml/min.) is measured, the cardiac output being the sum of the aortic andcoronary outputs (liquid issuing from the chamber 12 coming from the pulmonary artery and losses through the apex of the heart).
Phase 2: anaerobic pe iod During this period which lasts 30 or 45 minutes, the heart is perfused through the aorta at a constant xate of 15 ml/min. with a perfusion liquid gassed wi-th the non-oxygenated mixture. The solutions of substances to be treated are directly injected at the level of the aorta by the miniature pump 20 at a rate of 0.I5 ml/min., the final molar concentration of these substance~ being 5 mM. After a few minutes of the anaerobic period, the contractile function of the heart stops completely.
Phase 3: aerobic recoverY period The heart is again perfused through the left atrium (anterograde technique) with a perfusion liquid gassed with the oxygenated mixture. The cardiac output and the aortic pressure are measured 15 and 30 minutes after reoxygenation of the perfusion liquid. They are expressed as a percentage 25 of the values obtained before the anaerobic period.
Perfusion liquids The stock per~usion liquid used is a bicarbonate buffer solution of the Krebs-Henseleit type brought to the temper-ature of 37C and consisting of: 120 mM NaCl, 5 mM KCl, 30 2.5 mM CaC12, 25 mM NaHCO3, 1.2 mM KH2PO4, 1-2 mM MgSO4 and 10 mM sodium pyruvate or sodium lactate.
The substances to be tested were prepared on the day of the test and their p~ adjusted to 7.4 with NaOH. They were only added to the stock perfusion liquid during the 35 anaerobic phase.
~ , . , ..~
, ~C)~39 45 hearts were perfused with a stock perfusion liquid containing sodium pyruvate and 50 hearts with a stock per-fusion liquid containing sodium lactate, after which the cardiac function parameters were measured at the end of phase 1 (aerobic period). The results obtained are shown in Table 1 below:
Stock continuous perfusion liquid conta.ining Pyruvate Lactate Weight of wet hearts (g) 1.46 + 0.03 1.39 + 0.03 15 OutputS (ml/min.) Aortic 19.1 + 1.14 22.9 ~ 1.1 Coronary 30.2 + 1.3 27.3 + 1.01 Cardiac 49.3 + 1.46 50.2 + 1.36 ~ .
Systolic aortic pressure (kPa) 13.78 + 0.25 14.25 ~ 0.23 After an anaerobic period of 30 or 45 minutes (phase 2), during which some of the hearts were perfused with the solutions of substances indicated in Table 2 below, the functional recovery (phase 3) varied according to the nature of the substances supplied to the hearts during the anaerobic phase as shown in Table 2 below which indicates the proportion of hearts recovering a cardiac output after the anaerobic period.
.
~:
.
~7 [)~
Propor~ion of hearts Substrates recovering a cardiac output after an anaerobic ~eriod of Stock continuous Solutions of sub-perfusion liquid stances to be tes- 30 mins. 45 mins.
containing ted perfused dur-ing the anaerobic period Lactate (control) 1/3 Lactate Aspartate 4/4 0/10 Aspartate + glutam-ate + pyruvate* 1/3 -Pyruvate (control) 5/5 1/5 Acetoacetate 10/10 9/10 Pyruvate Acetoacetate +
glutamate* 4/4 0/4 ~-hydroxybutyrate 2/3 0/3 Note: The aspartate, the glutamate, the pyruvate and the acetoacetate are in the form of the sodium salt.
* When there are several perfused subs~ances (during the anaerobic period), they are success~vely introduced so . that their final individual concentration is 5 mM.
Remarks:
The majority of hearts in the control group receiving the lactate (stock perfusion liquid~ did not recover measurable functions after reoxygenation. The addition of aspartate to ~he stock perfusion liquid provided for functional recovery of all the hearts examined after an anaerobic per:iod of 30 minutes. The extra addi~ion of : ., ....
,~ ~
:. . . :-~.. ' ' " ~ ' - ::
,.:'' ~... .
~7~)199 1 glutamate appeared to interfere with the effect of the aspartate. In none of these groups was recovery observed after an anaerobic period of 45 minutes.
After an anaerobic period of 45 minutes in the presence of pyruvate (stock perfusion liquid), the proportion of hearts recovering a measurable output was significantly higher in the group receiving the acetoacetate than in the control group.
After an anaerobic period of 30 minutes, 95% of the hearts examined had recovered a measurable function. However, better recovery of the cardiac contractility was already noticeable in the group receiving the acetoacetate. Thus, the aortic pressure was 69 ~3% of its value before the anaerobic period and the cardiac output 34 +7~ of its value before the anaerobic period for the control group. For the group receiving the acetoacetate, the aortic pressure was 7~ + 3% of its value before the anaerobic period and the cardiac output 52 ~7% of its value before the anaerobic period.
The improvement in the tolerance by the heart of the anaerobic state produced by the acetoacetate was not enhanced but rather impaired by the addition of glutamate. In addition, the perfusion of ~-hydroxybutyrate did not have a protective effect.
~, : . ' , , - , , .
.~ -.
:
, , .: ,:
Claims (10)
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. The use of acetoacetic acid or one of its physiologically acceptable salts or esters for obtaining a pharmaceutical composition intended for the preservation of living tissue in the absence of oxygenation or in the event of insufficient oxygenation by the blood.
2. The use claimed in Claim 1 of sodium acetoacetate.
3. The use claimed in Claim 1 in the presence of pyruvic acid or a physiologically acceptable salt or ester thereof.
4. The use claimed in Claim 3 in the presence of sodium pyruvate.
5. The use claimed in Claim 1 or 2 in the presence of glucose.
6. The use claimed in Claim 1 in the form of an isotonic or slightly hypertonic, sterile physiological aqueous solution.
7. The use claimed in Claim 6 in the form of a perfusion solution or a cardioplegic solution for preservation of the heart during cardiac operations or transplantations.
8. A method for treating organs to preserve them outside living organisms, characterized in that said organs are perfused with a pharmaceutical composition containing aceto-acetic acid or a physiologically acceptable salt or ester thereof.
9. A method as claimed in Claim 8, characterized in that the pharmaceutical composition contains pyruvic acid or a physiologically acceptable salt or ester thereof.
10. A method as claimed in Claim 9, characterized in that the pharmaceutical composition contains sodium acetoacetate and sodium pyruvate.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP85111290A EP0215138B1 (en) | 1985-09-06 | 1985-09-06 | Preservation of living tissues |
| EP85111290.4 | 1985-09-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1270199A true CA1270199A (en) | 1990-06-12 |
Family
ID=8193747
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000516289A Expired - Fee Related CA1270199A (en) | 1985-09-06 | 1986-08-19 | Preservation of living tissue |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US4970143A (en) |
| EP (1) | EP0215138B1 (en) |
| CA (1) | CA1270199A (en) |
| DE (1) | DE3581407D1 (en) |
Families Citing this family (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IL74774A (en) * | 1984-04-23 | 1988-05-31 | Abbott Lab | Method for the preparation of immunocytochemical slides with a polylysine solution |
| JPH0714338B2 (en) * | 1988-03-01 | 1995-02-22 | 有限会社パラサイト | Continuous perfusion device using aeration |
| CH683485A5 (en) * | 1990-11-20 | 1994-03-31 | Pasteur Merieux Serums Vacc | infusion solutions, preservation and organ perfusion. |
| US5376524A (en) * | 1991-04-01 | 1994-12-27 | Thomas Jefferson University | Platelet storage medium containing acetate and phosphate |
| FR2676331B1 (en) * | 1991-05-17 | 1993-09-03 | Opsia Pharma | MEDIUM FOR CONSERVATION OF ORGANS, TISSUES OR CELLS. |
| EP0562188B1 (en) * | 1992-03-27 | 1998-09-30 | Chung-Ho Chen | Composition for tissues to sustain viability and biological functions in surgery and storage |
| US5390679A (en) * | 1993-06-03 | 1995-02-21 | Eli Lilly And Company | Continuous cardiac output derived from the arterial pressure waveform using pattern recognition |
| DE19527734A1 (en) * | 1995-07-28 | 1997-01-30 | Hubert Verhaag | Method and device for preserving tissues and organs, in particular transplant tissues and organs |
| US5667962A (en) * | 1996-03-18 | 1997-09-16 | Case Western Reserve University | Pyruvate thiolester for the prevention of reperfusion injury |
| US6086789A (en) * | 1996-03-18 | 2000-07-11 | Case Western Reserve University | Medical uses of pyruvates |
| WO1998004127A2 (en) * | 1996-07-25 | 1998-02-05 | Stanko Ronald T | Transplant solutions containing pyruvate and methods for transplantation |
| US6316038B1 (en) | 1997-03-17 | 2001-11-13 | Btg International Limited | Therapeutic compositions |
| US20090253781A1 (en) * | 2002-05-24 | 2009-10-08 | Btg International Limited | Therapeutic compositions |
| US6323237B1 (en) | 1997-03-17 | 2001-11-27 | Btg International Limited | Therapeutic compositions |
| DE19859771C1 (en) * | 1998-12-23 | 2000-08-24 | Sueddeutsche Kalkstickstoff | Water-soluble, stable pyruvic acid (salt) -containing formulation |
| US6846842B2 (en) * | 1999-10-07 | 2005-01-25 | Beth Israel Deconess Medical Center, Inc. | Pyruvate ester composition and method of use for resuscitation after events of ischemia and reperfusion |
| JP2004528307A (en) * | 2001-03-15 | 2004-09-16 | ユニバーシティ オブ ピッツバーグ オブ ザ コモンウェルス システム オブ ハイヤー エデュケーション | Use of pyruvate and / or derivatives thereof for the treatment of inflammatory conditions mediated by cytokines |
| AU2002254525B2 (en) * | 2001-04-04 | 2004-12-23 | Critical Therapeutics, Inc. | Method for preventing acute renal failure |
| AU2003228593B2 (en) * | 2002-04-17 | 2006-07-27 | Critical Therapeutics, Inc. | Pharmaceutical composition comprising an alpha-ketoalkanoic acid ester or -amine and lactic acid or a lactic acid salt |
| US20040170950A1 (en) * | 2002-09-12 | 2004-09-02 | Prien Samuel D. | Organ preservation apparatus and methods |
| US7132221B2 (en) * | 2003-09-12 | 2006-11-07 | Headway Technologies, Inc. | Method to print photoresist lines with negative sidewalls |
| US20050153271A1 (en) * | 2004-01-13 | 2005-07-14 | Wenrich Marshall S. | Organ preservation apparatus and methods |
| GB0420856D0 (en) * | 2004-09-20 | 2004-10-20 | Ketocytonyx Inc | Cns modulators |
| US7947736B2 (en) | 2004-07-16 | 2011-05-24 | Btg International Limited | Oligomeric compounds |
| US7485743B2 (en) * | 2004-07-20 | 2009-02-03 | Btg International Limited | Oligomeric ketone compounds |
| WO2006012490A2 (en) * | 2004-07-23 | 2006-02-02 | Ketocytonyx Inc. | Ketogenic saccharides |
| DK1796658T3 (en) * | 2004-09-21 | 2016-06-27 | Btg Int Ltd | dopaminergic mimetics |
| WO2006098767A2 (en) * | 2004-09-21 | 2006-09-21 | Ketocytonyx Inc. | Treatment of adhd |
| DE102005048625A1 (en) * | 2005-10-11 | 2007-04-12 | Universität Leipzig | System for non-cardioplegic preservation of donor hearts for transplantation, comprises an equipment for the preservation of donor hearts, coaxial aortic cannula, perfusion management, organ holding bag and perfusion solution |
| US20080145919A1 (en) * | 2006-12-18 | 2008-06-19 | Franklin Thomas D | Portable organ and tissue preservation apparatus, kit and methods |
| EP2146711A4 (en) * | 2007-04-12 | 2011-10-26 | Univ Minnesota | Ischemia/reperfusion protection compositions and methods of using |
| US10307398B2 (en) | 2016-09-20 | 2019-06-04 | Regents Of The University Of Minnesota | Resuscitation composition and methods of making and using |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2532183C3 (en) * | 1975-07-18 | 1982-03-04 | Behringwerke Ag, 3550 Marburg | Polyionic isotonic saline solution for the preservation of erythrocytes or for the perfusion and preservation of organs intended for transplantation |
| DE3366419D1 (en) * | 1982-06-04 | 1986-10-30 | Hoxan Kk | Method of preserving organ and apparatus for preserving the same |
| CA1264442A (en) * | 1984-06-22 | 1990-01-16 | Richard L. Veech | Electrolyte solutions and in vivo use thereof |
-
1985
- 1985-09-06 DE DE8585111290T patent/DE3581407D1/en not_active Expired - Fee Related
- 1985-09-06 EP EP85111290A patent/EP0215138B1/en not_active Expired - Lifetime
-
1986
- 1986-08-14 US US06/896,620 patent/US4970143A/en not_active Expired - Fee Related
- 1986-08-19 CA CA000516289A patent/CA1270199A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| US4970143A (en) | 1990-11-13 |
| EP0215138B1 (en) | 1991-01-16 |
| DE3581407D1 (en) | 1991-02-21 |
| EP0215138A1 (en) | 1987-03-25 |
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