Lidoca?ne test for easier and less time consuming assessment of liver function in several hepatic injury models
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  • 作者:Dorra Ben Said (1) (3)
    Ridha Ben Ali (1) (3)
    Henda Ferchichi (1) (3)
    Issam Salouage (1) (3)
    Lobna Ouanes (2) (3)
    Emna Ga?es (1) (3)
    Sameh Trabelsi (1) (3)
    Emna Kooli (1)
    Nadia Kourda (4)
    Jaouida Abdelmoula (5)
    Mohamed Lakhal (1) (3)
    Anis Klouz (1) (3)
  • 关键词:MEGX ; Liver metabolism ; Ex vivo ; Hypothermic ischemia ; Ischemia ; reperfusion ; Cirrhosis
  • 刊名:Hepatology International
  • 出版年:2011
  • 出版时间:December 2011
  • 年:2011
  • 卷:5
  • 期:4
  • 页码:941-948
  • 全文大小:443KB
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  • 作者单位:Dorra Ben Said (1) (3)
    Ridha Ben Ali (1) (3)
    Henda Ferchichi (1) (3)
    Issam Salouage (1) (3)
    Lobna Ouanes (2) (3)
    Emna Ga?es (1) (3)
    Sameh Trabelsi (1) (3)
    Emna Kooli (1)
    Nadia Kourda (4)
    Jaouida Abdelmoula (5)
    Mohamed Lakhal (1) (3)
    Anis Klouz (1) (3)

    1. Service de Pharmacologie Clinique, Centre National de Pharmacovigilance, Tunis, Tunisia
    3. Unité d’expérimentation animale, Faculté de Médecine de Tunis, Tunis, Tunisia
    2. Laboratoire de Physiologie, Faculté de Médecine de Tunis, Tunis, Tunisia
    4. Service Anatomo-pathologie, Hopital Charles Nicolle, Tunis, Tunisia
    5. Service de Biochimie, Hopital Charles Nicolle, Tunis, Tunisia
文摘
Purpose In this study, we developed an ex vivo functional assay to assess liver metabolic capacity adapted from the lidoca?ne test in rats. Methods Animals used were subjected to different models of liver injury: hypothermic ischemia (H/I, n?=?8), ischemia-reperfusion (I/R, n?=?8) and CCl4 induced liver cirrhosis (n?=?11), and compared with sham operated rats (n?=?5). Livers were then extracted and a fragment of whole tissue was incubated with lidoca?ne for 15, 30, 60, 120, 240, 360, and 720?min at which both lidoca?ne and its major metabolite monoethylglycinexylidide (MEGX) were measured by high performance liquid chromatography (HPLC). A histological study and biochemical assays (transaminase levels) were also performed to further evaluate and confirm our data. Results Pharmacokinetic profile of lidoca?ne metabolism in sham-operated animals revealed that the maximum concentration of MEGX is achieved at 120?min. Both lidoca?ne metabolism and MEGX formation levels were significantly altered in all three models of hepatic injury. The extent of hepatic damage was confirmed by increased levels of transaminase levels and alteration of hepatocyte’s structure with areas of necrosis. Conclusion Our method provides reliable and reproducible results using only a small portion of liver which allows for a fast and easy assessment of liver metabolic capacity. Moreover, our method presents an alternative to the in vivo technique and seems more feasible in a clinical setting.
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