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Jamshidzadeh, Akram, Dabagh, Fatemeh, Farshad, Omid, Ommat, Mohammad Mehdi, Mahdavinia, Azadeh, Azarpira, Negar, Shahbazi, Maryam, Najibi, Asma, Heidari, Reza. (1397). Hepatoprotective properties of the glycolipoprotein extract from Eisenia foetida. سامانه مدیریت نشریات علمی, 4(3), 149-160.
Akram Jamshidzadeh; Fatemeh Dabagh; Omid Farshad; Mohammad Mehdi Ommat; Azadeh Mahdavinia; Negar Azarpira; Maryam Shahbazi; Asma Najibi; Reza Heidari. "Hepatoprotective properties of the glycolipoprotein extract from Eisenia foetida". سامانه مدیریت نشریات علمی, 4, 3, 1397, 149-160.
Jamshidzadeh, Akram, Dabagh, Fatemeh, Farshad, Omid, Ommat, Mohammad Mehdi, Mahdavinia, Azadeh, Azarpira, Negar, Shahbazi, Maryam, Najibi, Asma, Heidari, Reza. (1397). 'Hepatoprotective properties of the glycolipoprotein extract from Eisenia foetida', سامانه مدیریت نشریات علمی, 4(3), pp. 149-160.
Jamshidzadeh, Akram, Dabagh, Fatemeh, Farshad, Omid, Ommat, Mohammad Mehdi, Mahdavinia, Azadeh, Azarpira, Negar, Shahbazi, Maryam, Najibi, Asma, Heidari, Reza. Hepatoprotective properties of the glycolipoprotein extract from Eisenia foetida. سامانه مدیریت نشریات علمی, 1397; 4(3): 149-160.

Hepatoprotective properties of the glycolipoprotein extract from Eisenia foetida

Trends in Pharmaceutical Sciences
مقاله 3، دوره 4، شماره 3، آذر 2018، صفحه 149-160    اصل مقاله (1005.78 K)
نوع مقاله: Research(Original) Article
نویسندگان
Akram Jamshidzadeh؛ Fatemeh Dabagh؛ Omid Farshad؛ Mohammad Mehdi Ommat؛ Azadeh Mahdavinia؛ Negar Azarpira؛ Maryam Shahbazi؛ Asma Najibi؛ Reza Heidari*
Shiraz University of Medical Sciences, Pharmaceutical Sciences Research Center
چکیده
The liver is continuously exposed to a variety of xenobiotics. Several xenobiotics are identified which act as hepatotoxicants. Hence, finding protective agents for ameliorating xenobiotics-included liver injury has a great value. Eisenia foetida, a kind of “earthworm,” is a source of a wide range of bioactive components. Several investigations have been evaluated the E. foetida extract (EFX) for biomedical and nutritional applications. The current study was designed to evaluate the potential hepatoprotective properties of EFX in two experimental models of hepatic damage. Acetaminophen (APAP; 1 g/kg, i.p) was administered as the animal model of acute liver injury in mice. Bile duct ligated (BDL) rats were used as the animal model of chronic hepatic damage. Severe elevation in tissue biomarkers of oxidative stress including lipid peroxidation and hepatic glutathione depletion was evident in both APAP-treated and BDL animals. Moreover, serum biomarkers of liver injury were drastically increased in both acute and chronic animal models of hepatotoxicity. Significant liver tissue histopathological alterations including tissue necrosis, vascular congestion, and inflammatory cells infiltration were detected in APAP-treated and BDL animals. On the other hand, it was found that EFX supplementation (100, 200, 500, and 700 mg/kg, i.p) mitigated oxidative stress markers, decreased serum biomarkers of liver injury, and alleviated liver tissue histopathological changes. The hepatoprotection provided by EFX supplementation in the current study might be mediated through its potential antioxidative mechanisms.
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