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Original Research Article | OPEN ACCESS

3-Cinnamoyl-4-hydroxy-6-methyl-2H-pyran-2-one ameliorates diabetic peripheral neuropathy in type 2 diabetes mellitus rats via PI3K/Akt signaling pathway

Xiaolei Li1, Suzhao Zhang2 , Gengliang Zhang1, Jun Yuan2, Shiling Rong1, Meng Wang3, Jie Wu1, Xiaoci Feng1, Huan He1, Linying Tian1, Weihua Xue2

1Department of Endocrinology; 2Department of Acupuncture, Hebei Hospital of Traditional Chinese Medicine, Shijiazhuang, Hebei 050011; 3Department of Endocrinology, Cangzhou Hospital of Integrated Traditional Chinese and Western Medicine Hebei, Cangzhou, Hebei 061899, China.

For correspondence:-  Suzhao Zhang   Email: SydneyGrimescdj@yahoo.com   Tel:+8631169095105

Accepted: 25 November 2019        Published: 30 December 2019

Citation: Li X, Zhang S, Zhang G, Yuan J, Rong S, Wang M, et al. 3-Cinnamoyl-4-hydroxy-6-methyl-2H-pyran-2-one ameliorates diabetic peripheral neuropathy in type 2 diabetes mellitus rats via PI3K/Akt signaling pathway. Trop J Pharm Res 2019; 18(12):2509-2514 doi: 10.4314/tjpr.v18i12.7

© 2019 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..

Abstract

Purpose: To investigate the curative effects of 3-cinnamoyl-4-hydroxy-6-methyl-2H-pyran-2-one (CHMP) on streptozotocin (STZ)-induced model of diabetic SD rats, and the underlying mechanism. 
Method: Diabetes was induced in rats using single intraperitoneal injection of STZ. Subsequently, diabetic and non-diabetic rats were randomly grouped into five experimental groups. Six weeks after the STZ-injection, the diabetic animals were orally administered test compound (CHMP) at two doses of 10 and 20 mg/kg body weight for 6 weeks. Thereafter, the rats were anesthetised, and body weight, blood sugar, and motor nerve conduction velocity (MNCV) were determined. Moreover, real time-polymerase chain reaction (RT-PCR) and western blot analysis were used to assay the expression levels of genes in PIK3/Akt pathway and Glut4.
Results: Treatment of diabetic rats with CHMP significantly reduced levels of fasting blood glucose and enhanced average rat body weight, relative to diabetic control (p F6; 0.05). Motor nerve conduction velocity (MNCV) was remarkably increased in CHMP-treated rats (54.2 ± 2.2), when compared to the diabetic control rats (46 ± 4.1, p < 0.01). Results from RT-PCR and western blot indicated increased expressions of PI3K, Akt and IRS-1, and down regulation of GSK-3B expression in skeletal muscle. The CHMP treatment also upregulated the Glut4 expression in skeletal muscle.
Conclusion: These findings show that CHMP may be beneficial in the management of diabetic neuropathy.

Keywords: Diabetic neuropathy, 3-Cinnamoyl-4-hydroxy-6-methyl-2H-pyran-2-one, Motor nerve conduction velocity, Streptozotocin, Hyperglycaemia

Impact Factor
Thompson Reuters (ISI): 0.523 (2021)
H-5 index (Google Scholar): 39 (2021)

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