Construction of porcine DCD marginal donor model and pathological observation of donor kidney
Basic Medicine|更新时间:2026-01-09
|
Construction of porcine DCD marginal donor model and pathological observation of donor kidney
Journal of Army Medical UniversityVol. 45, Issue 5, Pages: 426-432(2023)
作者机构:
1.400038 重庆,陆军军医大学(第三军医大学)第一附属医院麻醉科
2.400020 重庆,陆军第958医院麻醉科
3.400037 重庆,陆军军医大学(第三军医大学)第二附属医院泌尿外科
作者简介:
基金信息:
the Natural Science Foundation for Young Scholars of China(81801900);the General Program of Natural Science Foundation of Chongqing(cstc2018jcyjAX0007);the Talent Foundation of Army Medical University(XZ-2019-505-028)
Xiangfeng LIU, Qian CHEN, Zhigang QIN, et al. Construction of porcine DCD marginal donor model and pathological observation of donor kidney[J]. Journal of Army Medical University, 2023, 45(5): 426-432.
DOI:
Xiangfeng LIU, Qian CHEN, Zhigang QIN, et al. Construction of porcine DCD marginal donor model and pathological observation of donor kidney[J]. Journal of Army Medical University, 2023, 45(5): 426-432. DOI: 10.16016/j.2097-0927.202211138.
Construction of porcine DCD marginal donor model and pathological observation of donor kidney
To construct a marginal donor model of porcine donation after cardiac death (DCD)
and evaluate the pathological alteration of DCD donor kidneys.
Methods
2
Seven male mini pigs (4~6 months old
13~17 kg) were divided into standard donor control group (C group
n
=3) and DCD group (
n
=4). After intramuscular injection with phenobarbital sodium
their auricular vein channels were established
then propofol and sufentanil were injected to enhance the anesthetic induction while blood pressure
electrocardiogram and oxygen saturation (SaO
2
) were monitored at the same time. Group C received mechanical ventilation after endotracheal intubation
and maintained anesthesia with propofol
remifentanil and cisatracurium
and the kidneys were harvested under laparotomy. In the DCD group
300 IU/kg heparin was injected intravenously for anticoagulation
followed by single bolus venous injection with 600 mg propofol and 10 mg cisatricurium to induce cardiac and respiratory arrest
and finally
the kidneys were harvested i
n 30 min after cardiac arrest. The kidneys in both groups were cut into small tissues
which were further fixed with 4% paraformaldehyde
embedded in paraffin wax and stained with HE for the pathological assessment and tissue damage scores under a optical microscope.
Results
2
The mean time for SaO
2
to decline to 80% was 3.25±1.89 min and the mean time for cardiac arrest was 7.75±3.10 min in the 4 pigs of DCD group after injection with overdose of anesthetics. Compared with the C group
the renal tubular injury score of DCD marginal donor kidney after suffering from warm ischemia for 30 min
was higher (
P
<
0.05)
and the mean score of glomerular injury was increased through no statistical difference.
Conclusion
2
Intravenous injection of excessive propofol and cisatracurium can effectively establish a porcine DCD marginal donor model.
关键词
Keywords
references
BAUER A C, FRANCO R F, MANFRO R C. Immunosuppression in kidney transplantation: state of the art and current protocols[J]. Curr Pharm Des, 2020, 26(28): 3440-3450. DOI: 10.2174/1381612826666200521142448.
CHEN D, ZHANG W J. Evaluation and application of marginal donor liver[J]. J Clin Surg, 2018, 26(12): 893-895. DOI: 10.3969/j.issn.1005-6483.2018.12.001.
SMITH M, DOMINGUEZ-GIL B, GREER D M, et al . Organ donation after circulatory death: current status and future potential[J ] . Intensive Care Med, 2019, 45(3): 310-321. DOI: 10.1007/s00134-019-05533-0.
SUMMERS D M, WATSON C J E, PETTIGREW G J, et al . Kidney donation after circulatory death (DCD): state of the art[J ] . Kidney Int, 2015, 88(2): 241-249. DOI: 10.1038/ki.2015.88.
REEB J, KESHAVJEE S, CYPEL M. Expanding the lung donor pool: advancements and emergingpathways[J]. Curr Opin Organ Transplant, 2015, 20(5): 498-505. DOI: 10.1097/MOT.0000000000000233.
Organ Transplantation Branch of the Chinese Medical Association. Guidelines for organ donation of dead heart in China (2nd edition)[J]. Chin J Organ Transplant, 2011, 32(12): 756-758. DOI: 10.3760/cma.j.issn.0254-1785.2011.12.014
ROUFOSSE C, SIMMONDS N, CLAHSEN-VAN GRONINGEN M, et al . A 2018 reference guide to the Banff classification of renal allograft pathology[J ] . Transplantation, 2018, 102(11): 1795-1814. DOI: 10.1097/tp.0000000000002366.
ZHAO H L, NING J L, SAVAGE S, et al . A novel strategy for preserving renal grafts in an ex vivo setting: potential for enhancing the marginal donor pool[J ] . FASEB J, 2013, 27(12): 4822-4833. DOI: 10.1096/fj.13-236810..
ATTIA M, SILVA M A, MIRZA D F. The marginal liver donor: an update[J]. Transpl Int, 2008, 21(8): 713-724. DOI: 10.1111/j.1432-2277.2008.00696.x.
ALBANO L, BANAS B, LEHNER F, et al . Outcomes with tacrolimus-based immunosuppression after kidney transplantation from standard- and extended-criteria donors—A post hoc analysis of the prospective OSAKA study[J ] . Ann Transplant, 2020, 25: e920041. DOI: 10.12659/AOT.920041.
ISRANI A K, ZAUN D, HADLEY N, et al . OPTN/S RTR 2018 annual data report: deceased organ donation[J ] . Am J Transplant, 2020, 20(Suppl s1): 509-541. DOI: 10.1111/ajt.15678.
WANG P, MA J, ZUO Z C, et al . MRI-IVIM in mini-pig submandibular gland radiation injury: a preliminary study on the application of value[J ] . J Clin Radiol, 2017, 36(11): 1716-1720. DOI: 10.13437/j.cnki.jcr.2017.11.044.
CHEN W M, LI F, HUANG D D, et al . Experimental study on fasudil for increasing preserving effect on porcine DCD heart induced by ischemia[J ] . Chongqing Med, 2014, 43(36): 4864-4868. DOI: 10.3969/j.issn.1671-8348.2014.36.006.
YU M. Research on the algorithm used for artifacts suppression and ECG rhythm recognition during chest compression[D]. Beijing: Academy of Military Medical Sciences, 2017.
SANCHEZ P G, BITTLE G J, WILLIAMS K, et al . Ex vivo lung evaluation of prearrest heparinization in donation after cardiac death[J ] . Ann Surg, 2013, 257(3): 534-541. DOI: 10.1097/SLA.0b013e318273bef1.
GABISONIA K, PROSDOCIMO G, AQUARO G D, et al . MicroRNA therapy stimulates uncontrolled cardiac repair after myocardial infarction in pigs[J ] . Nature, 2019, 569(7756): 418-422. DOI: 10.1038/s41586-019-1191-6.
LIU L, LIU Y H, MA N, et al . Protective effect of extracorporeal membrane oxygenation on liver graft after cardiac death in pigs[J ] . Chin J Organ Transplant, 2015, 36(1): 44-47. DOI: 10.3760/cma.j.issn.0254-1785.2015.01.011
MA N, LIU L, LIU Y H, et al . Intestinal mucosal barrier function changes during reperfusion of donation after pig cardiac death by extracorporeal membrane oxygenation[J ] . J Tianjin Med Univ, 2020, 26(3): 209-212, 217.
FAN X L, HU L, CHEN Z Q, et al . Repair function of extracorporeal membrane oxygenation recirculation in vivo for swine liver after cardiac death[J ] . Chin J Organ Transplant, 2014, 35(7): 426-430. DOI: 10.3760/cma.j.issn.0254-1785.2014.07.011..
SHEN Y, LIU T W, CHEN M H, et al . A swine model of acute asphyxial cardiac arrest by endotracheal tube clamping[J ] . J Guangxi Med Univ, 2008, 25(3): 344-346. DOI: 10.16190/j.cnki.45-1211/r.2008.03.010.
IYER A, CHEW H C, GAO L, et al . Pathophysiological trends during withdrawal of life support: implications for organ donation after circulatory death[J ] . Transplantation, 2016, 100(12): 2621-2629. DOI: 10.1097/TP.0000000000001396.
BI J L, CAI M, YUAN Q, et al . Establishment of a miniature porcine model for controlled cardiac deceased donor[J ] . Chin J Organ Transplant, 2015, 36(12): 705-708. DOI: 10.3760/cma.j.issn.0254-1785.2015.12.001.
WANG S Y, ZHANG C Y, CAI G Y, et al . Method used to establish a large animal model of drug-induced acute kidney injury[J ] . Exp Biol Med (Maywood), 2021, 246(8): 986-995. DOI: 10.1177/1535370220981756.
SAFAEE FAKHR B, DONDOSSOLA D, CAVENAGO M, et al . Deterioration of lung function in a pig model of uncontrolled cardiac death[J ] . Transplant Proc, 2016, 48(2): 431-434. DOI: 10.1016/j.transproceed.2015.12.046.
Establishment and standardized modeling of lethal shock rat models in high-altitude, high-cold, and high-heat environments
Establishment of a rat model of infrarenal abdominal aortic aneurysm via retroperitoneal approach
Mechanism of hepatitis B virus X inducing hepatocellular carcinoma in mice through COX-2 and its downstream factors
Establishment and identification of a mouse model of Fscb/Cabyr double gene knockout
HBx gene accelerates cell proliferation and enhances inflammatory factors expression through ERK1/2 signaling pathway
Related Author
WU Yue
ZHU Yu
LI Qinghui
LI Tao
Junxing ZHU
Quanqiao TANG
Song FENG
Xingchi SHI
Related Institution
State Key Laboratory of Trauma and Chemical Poisoning, Department of War Trauma, Shock and Blood Transfusion, Daping Hospital, Army Medical University(Third Military Medical University)
Department of Clinical Medicine, North Sichuan Medical College, Nanchong
Department of Cardiovascular Diseases, Affiliated Hospital, North Sichuan Medical College, Nanchong
Department of Tissue and Embryology, Basic Medical College, North Sichuan Medical College, Nanchong
Molecular Medicine and Cancer Research Center, Department of Biochemistry and Molecular Biology, College of Basic Medical Sciences, Chongqing Medical University