Jiaotai pill (交泰丸) enhances insulin signaling through phosphatidylinositol 3-kinase pathway in skeletal muscle of diabetic rats
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Jiaotai pill (交泰丸) enhances insulin signaling through phosphatidylinositol 3-kinase pathway in skeletal muscle of diabetic rats
Jiaotai pill (交泰丸) enhances insulin signaling through phosphatidylinositol 3-kinase pathway in skeletal muscle of diabetic rats
中国结合医学杂志(英文版)2013年19卷第9期 页码:668-674
Affiliations:
Institute of Integrative Traditional Chinese and Western Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology,Wuhan,China
Author bio:
Funds:
Supported by grants from National Natural Science Foundation of China (No. 30801492)
Dong, H., Wang, Jh., Lu, Fe. et al. Jiaotai pill (交泰丸) enhances insulin signaling through phosphatidylinositol 3-kinase pathway in skeletal muscle of diabetic rats., Chin. J. Integr. Med. 19, 668–674 (2013). https://doi.org/10.1007/s11655-013-1560-1
Hui Dong, Jian-hong Wang, Fu-er Lu, et al. Jiaotai pill (交泰丸) enhances insulin signaling through phosphatidylinositol 3-kinase pathway in skeletal muscle of diabetic rats[J]. Chinese Journal of Integrative Medicine, 2013,19(9):668-674.
Dong, H., Wang, Jh., Lu, Fe. et al. Jiaotai pill (交泰丸) enhances insulin signaling through phosphatidylinositol 3-kinase pathway in skeletal muscle of diabetic rats., Chin. J. Integr. Med. 19, 668–674 (2013). https://doi.org/10.1007/s11655-013-1560-1DOI:
Hui Dong, Jian-hong Wang, Fu-er Lu, et al. Jiaotai pill (交泰丸) enhances insulin signaling through phosphatidylinositol 3-kinase pathway in skeletal muscle of diabetic rats[J]. Chinese Journal of Integrative Medicine, 2013,19(9):668-674. DOI: 10.1007/s11655-013-1560-1.
Jiaotai pill (交泰丸) enhances insulin signaling through phosphatidylinositol 3-kinase pathway in skeletal muscle of diabetic rats
摘要
To investigate the effect of Jiaotai Pill (交泰丸
JTP) at different constitutional proportions on insulin signaling through phosphatidylinositol 3-kinase (PI3K) pathway in the skeletal muscle of diabetic rats. The rat model of type 2 diabetes mellitus (T2DM) was established by intravenous injection of a small dose of streptozotoein plus high fat diet feeding. JTP at the same dosage of cinnamon and the increasing dosage of Coptis chinensis was administered to diabetic rats for nine weeks respectively. Plasma glucose and insulin levels were assayed. The expressions of proteins were determined by Western blot method. All the three formulations of JTP decreased plasma glucose and fasting insulin levels as well as increased the protein expressions of insulin receptor β (InsRβ) subunit
insulin receptor substrate-1 (IRS-1)
PI3K p85 subunit and glucose transporter 4 (GLUT4) in skeletal muscle. Meanwhile
JTP increased the tyrosine phosphorylation of InsRβ subunit and IRS-1
and reduced the serine phosphorylation of IRS-1 in skeletal muscle. Interestingly
the effect of JTP on improving insulin sensitivity was not dose-dependent. In contrast
JTP containing the least amount of Coptis chinensis exhibited the best effect. JTP at different constitutional proportions attenuates the development of diabetes in a rat model of T2DM. The mechanism might be associated with enhancing insulin signaling through PI3K pathway in the skeletal muscle.
Abstract
To investigate the effect of Jiaotai Pill (交泰丸
JTP) at different constitutional proportions on insulin signaling through phosphatidylinositol 3-kinase (PI3K) pathway in the skeletal muscle of diabetic rats. The rat model of type 2 diabetes mellitus (T2DM) was established by intravenous injection of a small dose of streptozotoein plus high fat diet feeding. JTP at the same dosage of cinnamon and the increasing dosage of Coptis chinensis was administered to diabetic rats for nine weeks respectively. Plasma glucose and insulin levels were assayed. The expressions of proteins were determined by Western blot method. All the three formulations of JTP decreased plasma glucose and fasting insulin levels as well as increased the protein expressions of insulin receptor β (InsRβ) subunit
insulin receptor substrate-1 (IRS-1)
PI3K p85 subunit and glucose transporter 4 (GLUT4) in skeletal muscle. Meanwhile
JTP increased the tyrosine phosphorylation of InsRβ subunit and IRS-1
and reduced the serine phosphorylation of IRS-1 in skeletal muscle. Interestingly
the effect of JTP on improving insulin sensitivity was not dose-dependent. In contrast
JTP containing the least amount of Coptis chinensis exhibited the best effect. JTP at different constitutional proportions attenuates the development of diabetes in a rat model of T2DM. The mechanism might be associated with enhancing insulin signaling through PI3K pathway in the skeletal muscle.
关键词
Jiaotai Pillinsulin signalingphosphatidylinositol 3-kinaseskeletal musclediabetes mellitusChinese Medicine
Keywords
Jiaotai Pillinsulin signalingphosphatidylinositol 3-kinaseskeletal musclediabetes mellitusChinese Medicine
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Text Mining of Rheumatoid Arthritis and Diabetes Mellitus to Understand the Mechanisms of Chinese Medicine in Different Diseases with Same Treatment
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Department of Cardiology, Affiliated Hospital of Shandong University of Traditional Chinese Medicine
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