Abstract | OBJECTIVE: METHODS: The type 2 diabetic model was established using high fat diet and intraperitoneal injection of small dose streptozotocin (STZ). The Pi- yin deficiency model was established referring to classic compound factors. The learning and memory capabilities were tested in rats by the behavioral changes. The protein expressions of hippocampal IRE1alpha, JNK, and IRS-1 were detected using Western blot. RESULTS: There was statistical difference in the learning and memory capabilities of Pi- yin deficiency rats when compared with the blank control group (P<0.05). The learning and memory capabilities could be improved by ZBPYR. The protein expressions of hippocampal phospho-IRS-1, phospho-JNK, and total IRE1alpha were enhanced (P<0.05). But they were weakened after treatment of ZBPYR. CONCLUSIONS: ZBPYR could significantly improve the learning and memory capabilities of Pi- yin deficiency diabetic rats. Its functions might be correlated with improving the endoplasmic reticulum stress to regulate the insulin signaling pathway.
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Authors | Li-Na Liang, Shou-Yu Hu, Li-Bin Zhan |
Journal | Zhongguo Zhong xi yi jie he za zhi Zhongguo Zhongxiyi jiehe zazhi = Chinese journal of integrated traditional and Western medicine
(Zhongguo Zhong Xi Yi Jie He Za Zhi)
Vol. 32
Issue 3
Pg. 356-61
(Mar 2012)
ISSN: 1003-5370 [Print] China |
PMID | 22686083
(Publication Type: Journal Article, Research Support, U.S. Gov't, Non-P.H.S.)
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Chemical References |
- Drugs, Chinese Herbal
- Ern1 protein, rat
- Insulin
- Insulin Receptor Substrate Proteins
- Irs1 protein, rat
- Multienzyme Complexes
- zibu piyin
- Protein Serine-Threonine Kinases
- JNK Mitogen-Activated Protein Kinases
- Endoribonucleases
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Topics |
- Animals
- Diabetes Mellitus, Experimental
(drug therapy, metabolism)
- Drugs, Chinese Herbal
(pharmacology, therapeutic use)
- Endoplasmic Reticulum Stress
- Endoribonucleases
(metabolism)
- Hippocampus
(drug effects, metabolism)
- Insulin
(metabolism)
- Insulin Receptor Substrate Proteins
(metabolism)
- Insulin Resistance
- JNK Mitogen-Activated Protein Kinases
(metabolism)
- Male
- Multienzyme Complexes
(metabolism)
- Protein Serine-Threonine Kinases
(metabolism)
- Rats
- Rats, Sprague-Dawley
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