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Study on the antidiabetic mechanism of a shark liver peptide, S-8300, in alloxan-induced diabetes.
Huang, Fengjie; Wu, Wutong.
Affiliation
  • Huang F; School of life Science and Technology, China Pharmaceutical University, Nanjing, China.
J Pharm Pharmacol ; 61(6): 789-94, 2009 Jun.
Article in En | MEDLINE | ID: mdl-19505370
ABSTRACT

OBJECTIVES:

The aim was to evaluate the antidiabetic mechanism of S-8300 in alloxan-diabetic mice.

METHODS:

Diabetes was induced by a single intravenous injection of alloxan (60 mg/kg). The effects of S-8300 on diabetic mice were investigated by observing the change in fasting plasma glucose, detecting Fas mRNA by reverse transcriptase-polymerase chain reaction, Fas protein expression in the pancreas by immunohistochemistry and Western blot, and the DNA fragmentation pattern forming a ladder by electrophoresis. KEY

FINDINGS:

A significant decrease in fasting plasma glucose was observed, and Fas mRNA and Fas protein expression in the pancreas were attenuated in diabetic mice treated with S-8300. Treatment with S-8300 also attenuated DNA ladder formation.

CONCLUSIONS:

The results suggest that S-8300 inhibits Fas protein-mediated apoptosis of pancreas cells.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Peptides / Diabetes Mellitus, Experimental / Hypoglycemic Agents / Liver Extracts Limits: Animals Language: En Journal: J Pharm Pharmacol Year: 2009 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Peptides / Diabetes Mellitus, Experimental / Hypoglycemic Agents / Liver Extracts Limits: Animals Language: En Journal: J Pharm Pharmacol Year: 2009 Document type: Article Affiliation country: