Journals / Gülhane Tıp Dergisi / 2021 / Cilt: 63 - Sayı: 2

Optimal time for remote ischemic preconditioning for liver protection in experimental major liver resection

Pages
129–135
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Conclusions: Remote IPC protocols we studied in this experiment did not blunt hepatic IRI in rodents.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Aims: Due to the liver’s rich blood supply, the control of inflow is mandatory if major resection is being planned.
📊
Key Findings & Data:Remote ischemic preconditioning (IPC) was shown to ameliorate injury in the target organ in various animal models.
💡
Conclusion & Impact:Conclusions: Remote IPC protocols we studied in this experiment did not blunt hepatic IRI in rodents.
🔬Design:Modeling & Simulation
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Özet

Aims: Due to the liver’s rich blood supply, the control of inflow is mandatory if major resection is being planned. In this regard, temporary portal triad clamping is widely used. However, ischemia-reperfusion injury (IRI) in the liver is inevitable following interruption. Remote ischemic preconditioning (IPC) was shown to ameliorate injury in the target organ in various animal models. This experimental animal study was conducted to determine optimal preconditioning frequency to use in liver surgery that promotes potential mediators associated with protection. Methods: Male Wistar-Albino rats (n=72) were divided into 8 groups. In group 1 (sham), only the left lobe of the liver was resected without any preconditioning. In group 2, the left lobe of the liver was resected using 30 min of portal triad clamping. In other groups, prior to resection using the same procedure with group 2, 6 different remote IPC protocols (5 to 10 min ischemia plus 10 to 20 min reperfusion) were applied by clamping the femoral artery. Serum tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6) level analysis, liver function tests, and histological examination were performed using the TUNEL staining to study apoptosis. Results: Compared to group 2, serum serum TNF-α and IL-6 level analysis and liver function tests did not show any difference. There was also no difference between the intervention groups and controls in histopathologic examination and apoptotic cell counts. Conclusions: Remote IPC protocols we studied in this experiment did not blunt hepatic IRI in rodents.

🔖

Cite This Article

ALAKUŞ, Ü., CAN, M. F., AYDIN, F. N., ÖZTAŞ, M., ÖZERHAN, İ. H., SARIGÖZ, T., ŞİMŞEK, A., PEKER, Y. (2021). Optimal time for remote ischemic preconditioning for liver protection in experimental major liver resection. Gülhane Tıp Dergisi, Cilt: 63 - Sayı: 2, 129–135. https://ajindex.com/articles/347983

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (14)

  1. Kim YI. Ischemia-reperfusion injury of the human liver during hepatic resection. J Hepatobiliary Pancreat Surg. 2003;10:195-199
  2. Jaeschke H. Molecular mechanisms of hepatic ischemiareperfusion injury and preconditioning. Am J Physiol Gastrointest Liver Physiol. 2003;284:G15-G26
  3. Reimer KA, Murry CE, Yamasawa I, Hill ML, Jennings RB. Four brief periods of myocardial ischemia cause no cumulative ATP loss or necrosis. Am J Physiol Heart Circ. 1986;251:H1306-H1315
  4. Murry CE, Jennings RB, Reimer KA. Preconditioning with ischemia: a delay of lethal cell injury in ischemic myocardium. Circulation. 1986;74:1124-1136
  5. Yao A, Li X, Pu L, et al. Impaired hepatic regeneration by ischemic preconditioning in a rat model of small-for-size liver transplantation. Transpl Immunol. 2007;18:37-43
  6. Eipel C, Glanemann M, Nuessler AK, Menger MD, Neuhaus P, Vollmar B. Ischemic preconditioning impairs liver regeneration in extended reduced-size livers. Ann Surg. 2005;241:477-484
  7. Przyklenk K, Bauer B, Ovize M, Kloner RA, Whittaker P. Regional ischemic ‘preconditioning’ protects remote virgin myocardium from subsequent sustained coronary occlusion. Circulation. 1993;87:893-899
  8. Kharbanda RK, Mortensen UM, White PA, et al. Transient limb ischemia induces remote ischemic preconditioning in vivo. Circulation. 2002;106:2881-2883
  9. Kanoria S, Jalan R, Davies NA, Seifalian AM, Williams R, Davidson BR. Remote ischaemic preconditioning of the hind limb reduces experimental liver warm ischaemiareperfusion injury. Br J Surg. 2006;93:762-768
  10. Magyar Z, Varga G, Mester A, et al. Is the early or delayed remote ischemic preconditioning the more effective from a microcirculatory and histological point of view in a rat model of partial liver ischemia-reperfusion? Acta Cirurgica Brasileira. 2018;33:597-608
  11. Camargo CA Jr, Madden JF, Gao W, Selvan RS, Clavien PA. Interleukin-6 protects liver against warm ischemia/ reperfusion injury and promotes hepatocyte proliferation in the rodent. Hepatology. 1997;26:1513-1520
  12. Lai IR, Chang KJ, Tsai HW, Chen CF. Pharmacological preconditioning with simvastatin protects liver from ischemia-reperfusion injury by heme oxygenase-1 induction. Transplantation. 2008;85:732-738
  13. Pringle JH. V. Notes on the arrest of hepatic hemorrhage due to trauma. Ann Surg. 1908;48:541-549
  14. Yadav SS, Sindram D, Perry DK, Clavien PA. Ischemic preconditioning protects the mouse liver by inhibition of apoptosis through a caspase-dependent pa