Experimental study on the preservation of amputated limb by low-temperature HTK preservation solution arterial perfusion

Shi Zhuang, Bayarmaa Enkhbat, Sergelen Orgoi, Sayamaa Lkhagvadorj

Article ID: 4400
Vol 8, Issue 1, 2024

VIEWS - 298 (Abstract) 126 (PDF)

Abstract


Objective: To evaluate the effect of HTK (Histidine-Tryptophan-Ketoglutarate solution) infusion on the protection and replantation of amputated limb. Methods: In experiment 1, the amputated limbs of male New Zealand white rabbits were preserved by different preservation methods, including low-temperature HTK solution perfusion group, low-temperature normal saline perfusion group, low-temperature preservation group and non-perfusion group at normal temperature. The homogenates of muscle tissue at different time points were collected for biochemical detection. H&E (hematoxylin and eosin) staining was performed on muscle tissue. Bax, Bcl-2 protein immunohistochemical staining and Tunel method were used to detect apoptosis in muscle, nerve, and vascular tissues. The ultrastructure of cells was observed by transmission electron microscope. In experiment 2, the amputated limbs of rabbits were treated with HTK perfusion and cryopreservation without perfusion, respectively. The survival of rabbits and their limbs were observed, and detected by H&E, TUNEL (Terminal deoxynucleotidyl transferase dUTP Nick End Labeling) and scanning electron microscopy. Statistical analysis was performed using SPSS 22 (SPSS Inc., Chicago, IL, USA). χ2 test, student’s t-test, and ANOVA (Analysis of Variance) were used to compare the categorical and continuous variables. Results: Experiment 1: With the extension of disconnection time, there were statistical differences between the biochemical indexes of the HTK liquid perfusion group and those of the non-low temperature non-perfusion group, while some indexes of the other groups were different. Immunohistochemical staining of tissues (muscle, nerve, and blood vessel) in each group showed that the number of cells stained by anti-apoptotic protein BCL-2 in each group significantly increased with the extension of time, while the number of cells stained by pro-apoptotic protein BAX2 in each group significantly decreased. Tunel test showed that compared with other treatment groups, the apoptosis rate of the HTK liquid group was significantly decreased. Experiment 2: The survival rate of the experimental group was 60%, and that of the control group was only 30%. H&E staining, the TUNEL method and scanning electron microscopy suggested that HTK infusion could reduce ischemia-reperfusion injury in muscle tissue. Conclusion: 1. Perfusion preservation of severed limbs at 4 ℃ can effectively reduce tissue damage caused by ischemia and hypoxia, and the effect is stronger than direct preservation. 2. HTK solution and normal saline were used for one-time perfusion of the severed limbs of rabbits, and the preservation effect of HTK solution was the best. 3. HTK solution was used for one-time perfusion of severed hind limbs of rabbits, which was refrigerated at 4 ℃ and then replanted (ischemia time was 3–5 h). Compared with the replanted limbs after cold storage alone, the survival rate was higher, and the postoperative ischemia and hypoxia injury of surviving limbs were less.


Keywords


amputated limb; organ preservation solution; perfusion; HTK infusion; back planting

Full Text:

PDF


References


1. Krezdorn N, Sakthivel D, Turk M, et al. Reduced Hypoxia-Related Genes in Porcine Limbs in Ex Vivo Hypothermic Perfusion Versus Cold Storage. Journal of Surgical Research. 2018; 232: 137-145. doi: 10.1016/j.jss.2018.05.067

2. Kueckelhaus M, Dermietzel A, Alhefzi M, et al. Acellular Hypothermic Extracorporeal Perfusion Extends Allowable Ischemia Time in a Porcine Whole Limb Replantation Model. Plastic & Reconstructive Surgery. 2017; 139(4): 922e-932e. doi: 10.1097/prs.0000000000003208

3. Ozer K. Advances in Limb Preservation: From Replantation to Transplantation. The Journal of Hand Surgery. 2020; 45(7): 626-637.e5. doi: 10.1016/j.jhsa.2020.04.006

4. Lindell SL, Compagnon P, Mangino MJ, et al. UW Solution for Hypothermic Machine Perfusion of Warm Ischemic Kidneys. Transplantation. 2005; 79(10): 1358-1361. doi: 10.1097/01.tp.0000159143.45022.f6

5. Wei J, Chang CY, Chuang YC, et al. Successful Heart Transplantation After 13 Hours of Donor Heart Ischemia With the Use of HTK Solution: A Case Report. Transplantation Proceedings. 2005; 37(5): 2253-2254. doi: 10.1016/j.transproceed.2005.03.055

6. Wilson CRH. Brook N, Talbot D. Preservation Solutions for Solid Organ Transplantation. Mini-Reviews in Medicinal Chemistry. 2006; 6(10): 1081-1090. doi: 10.2174/138955706778560148

7. Jamieson RW. Organ reperfusion and preservation. Frontiers in Bioscience. 2008; 13(13): 221. doi: 10.2741/2672

8. Allen FM. Resistance of peripheral tissue to asphyxia at various temperature. Surg Gynec Obstel. 1938; 67: 746-749.

9. Gao D, Li Q, Zhang Q, et al. Comparison of the effects of UW solution, Celsius solution, and HTK solution on low-temperature preservation of L-02 cells for bioartificial live. Guangdong Medical Journal. 2011; 32 (08): 962-965. doi: 10.13820/j.cnki. gdyx. 2011.08.029

10. Hachida M, Lu H, Ohkado A, et al. Effect of ATP-potassium channel opener nicorandil on long-term cardiac preservation. Journal of Cardiovascular Surgery. 2000; 41(4): 533.

11. Guha M, Kumar S, Choubey V, et al. Apoptosis in liver during malaria: role of oxidative stress and implication of mitochondrial pathway. The FASEB Journal. 2006; 20(8): 1224-1226. doi: 10.1096/fj.05-5338fje

12. Jia X, Yang H. Effect of various methods of tissue storage on split-skin viability at 4 ℃. Chinese Journal of Surgery. 1998; 36(011): 694-696.

13. Kober IM, Obermayr RP, Brüll T, et al. Comparison of the Solutions of Bretschneider, St. Thomas’ Hospital and the National Institutes of Health for Cardioplegic Protection during Moderate Hypothermic Arrest. European Surgical Research. 1998; 30(4): 243-251. doi: 10.1159/000008583

14. Başaran Ö, Özdemir H, Kut A, et al. Effects of different preservation solutions on skin graft epidermal cell viability and graft performance in a rat model. Burns. 2006; 32(4): 423-429. doi: 10.1016/j.burns.2005.11.010

15. Li Y. Diagnostic significance analysis of serum transaminase and creatine kinase measurements in patients with skeletal muscle diseases. Chinese and Foreign Medical Journal. 2014; 33(21): 23-25. doi: 10.16662/j.cnki.1674-0742.2014.21.051

16. Yan C, Qu SL, Wang J, Zou JN. Effect of adrenomedulin on skeletal muscle ischemia/reperfusion injury in rats. Journal of Clinical Rehabilitative Tissue Engineering Research. 2009; 13(2): 292-295.

17. Shang G, Guo X, Wang D, et al. The effect of cervical sympathetic nerve block on skeletal muscle ischemia-reperfusion injury. Chinese Journal of Modern Medicine. 2014; 24(29): 18-22.

18. Yan C, Qu S, Wang J, Zou J. The effect of adrenomedullin on skeletal muscle ischemia-reperfusion injury. Chinese Journal of Tissue Engineering Research and Clinical Rehabilitation. 2009; 13(2): 292-295.

19. Baird MF, Graham SM, Baker JS, et al. Creatine-Kinase- and Exercise-Related Muscle Damage Implications for Muscle Performance and Recovery. Journal of Nutrition and Metabolism. 2012; 2012: 1-13. doi: 10.1155/2012/960363

20. Xu C, Gao Y, Liang S. The function and diseases of P2 receptors in skeletal muscle. Chinese Pharmacological Bulletin. 2010; 26(2): 144-147.

21. Wan F, Zhao X, Liu B, Li J. Study on the protective effect of ligustrazine on myocardial ischemia-reperfusion injury in rats. Chinese Journal of Clinical Pharmacology and Therapeutics. 1998; 3: 184-186.

22. Chen W, Liu N, Zhang Y, et al. Exogenous hydrogen sulfide protects against myocardial injury after skeletal muscle ischemia/reperfusion by inhibiting inflammatory cytokines and oxidative stress in rats. Journal of Southern Medical University. 2013; 33(4): 554-558.

23. Lancerotto L, Tocco I, Salmaso R, et al. Necrotizing fasciitis. Journal of Trauma and Acute Care Surgery. 2012; 72(3): 560-566. doi: 10.1097/ta.0b013e318232a6b3

24. Zhou F. Pathophysiology of tissue blood perfusion and microcirculation - Oxidative stress and diseases. Surgical Theory and Practice. 2007; 6: 625-632.

25. Wang G, Li R, Zhang Z, et al. The effect of temperature on irreversible degeneration of rabbit skeletal muscle cells. Journal of Jilin University (Medical Edition). 2002; 5: 501-503. doi: 10.13481/j.1671-587x.2002.05.026

26. Ikeda H, Suzuki Y, Suzuki M, et al. Apoptosis is a major mode of cell death caused by ischaemia and ischaemia/reperfusion injury to the rat intestinal epithelium. Gut. 1998; 42(4): 530-537. doi: 10.1136/gut.42.4.530

27. Capano M, Crompton M. Bax translocates to mitochondria of heart cells during simulated ischaemia: involvement of AMP-activated and p38 mitogen-activated protein kinases. Biochemical Journal. 2006; 395(1): 57-64. doi: 10.1042/bj20051654

28. Fiskum G. Mitochondrial Participation in Ischemic and Traumatic Neural Cell Death. Journal of Neurotrauma. 2000; 17(10): 843-855. doi: 10.1089/neu.2000.17.843

29. Chen CJ, Cheng FC, Liao SL, et al. Effects of naloxone on lactate, pyruvate metabolism and antioxidant enzyme activity in rat cerebral ischemia/reperfusion. Neuroscience Letters. 2000; 287(2): 113-116. doi: 10.1016/S0304-3940(00)01151-4

30. Li P, Deepak N, Imawati B, et al. Cytochrome c and dATP-Dependent Formation of Apaf-1/Caspase-9 Complex Initiates an Apoptotic Protease Cascade. Cell. 2004; 116: 479-489.

31. Pan Dixit G, O’Rourke K, Vishva. Cell Biology and Metabolism: Caspase-9, Bcl-XL, and Apaf-1 Form a Ternary Complex.

32. Wang G, Wang G, Xu Z. Experimental study on the dynamic changes of GPT, ALP, and Glu in skeletal muscle of ischemic human body at room temperature. Journal of Norman Bethune Medical University. 1999; 5: 632-633. doi: 10.13481/j.1671-587x.1999.05.044

33. Shen Q, Yu Z, Fa J, et al. Morphological characteristics of several apoptotic cells under electron microscopy. Journal of Fudan University (Medical Edition). 2010; 37(3): 322-325.

34. Hettiaratchy S, Randolph MA, Andrew Lee WP. Long-term consideration of hand transplantation. Transplantation. 2003; 75(9): 1605. doi: 10.1097/01.tp.0000059447.40513.fb

35. Atkins SE, Winterton RIS, Kay SP. (v) Upper limb amputations: Where, when and how to replant. Current Orthopaedics. 2008; 22(1): 31-41. doi: 10.1016/j.cuor.2008.02.001

36. Lloyd MS, Teo TC, Pickford MA, et al. Preoperative management of the amputated limb. Emergency Medicine Journal. 2005; 22(7): 478-480. doi: 10.1136/emj.2003.008797




DOI: https://doi.org/10.24294/ti.v8.i1.4400

Refbacks

  • There are currently no refbacks.


Copyright (c) 2024 Shi Zhuang, Bayarmaa Enkhbat, Sergelen Orgoi, Sayamaa Lkhagvadorj

License URL: https://creativecommons.org/licenses/by-nc/4.0/

This site is licensed under a Creative Commons Attribution 4.0 International License.