2009Journal of Hepatopancreatobiliary SurgeryRequires access

Observation of arginine’s protection from hepatic injury and its effect on hepatic cell apoptosis in the rats with obstructive jaundice

Yang Shulong

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Abstract

Objective To explore whether arginine could lighten the hepatic dysfunction of rat with obstructive jaundice (OJ) and the influence of arginine on hepatic cell apoptosis. Methods A total of 42 adult Wistar rats were studied. They were divided into three groups: the sham operation group (A group), the OJ group (B group) and the group of OJ rats administered arginine (C group). The B and C group were established by double-ligating bile duct (BDL). Abdomenal injections of arginine (500 mg/kg·d) postoperatvely was administered daily in C group. Three groups of rats were sacrificed after 1 and 2 weeks of postoperation, respectively. The levels of serum total bilirubin (TBIL) , direct bilirubin (DBIL), alanine aminotransferase (ALT) and aspartate aminotransferase (AST) were tested and the tissue’s histopathology and ultrastructure changes were observed; the immunohistochemical technique was used for detecting the Bcl-2 and Bax protein expression. Results With the time of BDL extending, the values of serum ALT, AST, TBIL and DBIL were increased and the value of B group was higher than that of A group (P0.05); following that cell apoptosis increased apparently in hepatic tissue. Compared with B group, the injury degree of hepatic function and histopathology of changes in C group were decreased. With the time extending, the Bcl-2 and Bax protein of both B and C group were increased. The Bcl-2 was increased more evidently in C group, just like Bax in B group. Conclusion Arginine can ease the degree of hepatic functional injury, for it may decrease cell apoptosis by up-regulating the expression of Bcl-2 and down-regulating the expression of Bax in hepatic tissue.

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Objective To explore whether arginine could lighten the hepatic dysfunction of rat with obstructive jaundice (OJ) and the influence of arginine on hepatic cell apoptosis. Methods A total of 42 adult Wistar rats were studied. They were divided into three groups: the sham operation group (A group), the OJ group (B group) and the group of OJ rats administered arginine (C group). The B and C group were established by double-ligating bile duct (BDL). Abdomenal injections of arginine (500 mg/kg·d) postoperatvely was administered daily in C group. Three groups of rats were sacrificed after 1 and 2 weeks of postoperation, respectively. The levels of serum total bilirubin (TBIL) , direct bilirubin (DBIL), alanine aminotransferase (ALT) and aspartate aminotransferase (AST) were tested and the tissue’s histopathology and ultrastructure changes were observed; the immunohistochemical technique was used for detecting the Bcl-2 and Bax protein expression. Results With the time of BDL extending, the values of serum ALT, AST, TBIL and DBIL were increased and the value of B group was higher than that of A group (P0.05); following that cell apoptosis increased apparently in hepatic tissue. Compared with B group, the injury degree of hepatic function and histopathology of changes in C group were decreased. With the time extending, the Bcl-2 and Bax protein of both B and C group were increased. The Bcl-2 was increased more evidently in C group, just like Bax in B group. Conclusion Arginine can ease the degree of hepatic functional injury, for it may decrease cell apoptosis by up-regulating the expression of Bcl-2 and down-regulating the expression of Bax in hepatic tissue.

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Available abstract

Objective To explore whether arginine could lighten the hepatic dysfunction of rat with obstructive jaundice (OJ) and the influence of arginine on hepatic cell apoptosis. Methods A total of 42 adult Wistar rats were studied. They were divided into three groups: the sham operation group (A group), the OJ group (B group) and the group of OJ rats administered arginine (C group). The B and C group were established by double-ligating bile duct (BDL). Abdomenal injections of arginine (500 mg/kg·d) postoperatvely was administered daily in C group. Three groups of rats were sacrificed after 1 and 2 weeks of postoperation, respectively. The levels of serum total bilirubin (TBIL) , direct bilirubin (DBIL), alanine aminotransferase (ALT) and aspartate aminotransferase (AST) were tested and the tissue’s histopathology and ultrastructure changes were observed; the immunohistochemical technique was used for detecting the Bcl-2 and Bax protein expression. Results With the time of BDL extending, the values of serum ALT, AST, TBIL and DBIL were increased and the value of B group was higher than that of A group (P0.05); following that cell apoptosis increased apparently in hepatic tissue. Compared with B group, the injury degree of hepatic function and histopathology of changes in C group were decreased. With the time extending, the Bcl-2 and Bax protein of both B and C group were increased. The Bcl-2 was increased more evidently in C group, just like Bax in B group. Conclusion Arginine can ease the degree of hepatic functional injury, for it may decrease cell apoptosis by up-regulating the expression of Bcl-2 and down-regulating the expression of Bax in hepatic tissue.

Key concepts: Histopathology, Internal medicine, Apoptosis, Bilirubin, Immunohistochemistry, Group A, Arginine, Group B

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