Fuzhu jiangtang granules combined with metformin reduces insulin resistance in skeletal muscle of diabetic rats via PI3K/Akt signaling

Context: Fuzhu Jiangtang Granules (FJG) are a traditional Chinese used in the treatment of diabetes mellitus. However, the antidiabetic mechanism of FJG is not clear. Objective: This study evaluates and determines the antidiabetic mechanism of FJG using a Zucker diabetic fatty (ZDF) rat model. Mater...

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Autores principales: Yunsong Cao, Wen Sun, Guangyuan Xu
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Lenguaje:EN
Publicado: Taylor & Francis Group 2019
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Acceso en línea:https://doaj.org/article/648608daf3464d95a19ce64301bfba19
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spelling oai:doaj.org-article:648608daf3464d95a19ce64301bfba192021-11-17T14:21:56ZFuzhu jiangtang granules combined with metformin reduces insulin resistance in skeletal muscle of diabetic rats via PI3K/Akt signaling1388-02091744-511610.1080/13880209.2019.1659831https://doaj.org/article/648608daf3464d95a19ce64301bfba192019-01-01T00:00:00Zhttp://dx.doi.org/10.1080/13880209.2019.1659831https://doaj.org/toc/1388-0209https://doaj.org/toc/1744-5116Context: Fuzhu Jiangtang Granules (FJG) are a traditional Chinese used in the treatment of diabetes mellitus. However, the antidiabetic mechanism of FJG is not clear. Objective: This study evaluates and determines the antidiabetic mechanism of FJG using a Zucker diabetic fatty (ZDF) rat model. Materials and methods: ZDF (fa/fa) rats were divided into four groups (n = 6): diabetes mellitus (DM), metformin (Met, 0.134 g/kg b.w./day), FJG (0.64 g/kg b.w./day), and combination (Com, 0.134 g/kg b.w./day of Met and 0.64 g/kg b.w./day of FJG). Six ZDF (fa/+) rats served as a normal control. After 6 weeks, biochemical parameters gene and protein expression were detected. Results: The FBG, bodyweight, triglyceride (TG), total cholesterol (TC), free fatty acid (FFA), insulin levels, and HOMA-IR were lower in the FJG than in the DM group (p < 0.05, p < 0.01). In an oral glucose tolerance test, the AUC in the FJG group was significantly lower (p < 0.01). The levels of superoxide dismutase and catalase were higher in the FJG than in the DM group (p < 0.01); the malondialdehyde content and TNF-α were significantly decreased in the FJG group (p < 0.01). FJG increased the mRNA expression of IR and GLUT4 significantly (p < 0.05, p < 0.01). The protein levels of IR, p-IRS1 tyr989, m-PI3Kp85, p-Akt and GLUT4 were increased in the FJG (p < 0.05, p < 0.01), but the protein levels of p-IRS1 ser1101/612/307 were significantly decreased in the JG group (p < 0.01). Discussion and conclusions: The antidiabetic mechanism of FJG may be related to regulation of the insulin-signaling pathway in skeletal muscle. These aspects require further research.Yunsong CaoWen SunGuangyuan XuTaylor & Francis Grouparticleantidiabetic drugschinese herbal formulaanti-obesityantihypoglycemicantihypolipidemicantioxidantinsulin signaling pathwayTherapeutics. PharmacologyRM1-950ENPharmaceutical Biology, Vol 57, Iss 1, Pp 660-668 (2019)
institution DOAJ
collection DOAJ
language EN
topic antidiabetic drugs
chinese herbal formula
anti-obesity
antihypoglycemic
antihypolipidemic
antioxidant
insulin signaling pathway
Therapeutics. Pharmacology
RM1-950
spellingShingle antidiabetic drugs
chinese herbal formula
anti-obesity
antihypoglycemic
antihypolipidemic
antioxidant
insulin signaling pathway
Therapeutics. Pharmacology
RM1-950
Yunsong Cao
Wen Sun
Guangyuan Xu
Fuzhu jiangtang granules combined with metformin reduces insulin resistance in skeletal muscle of diabetic rats via PI3K/Akt signaling
description Context: Fuzhu Jiangtang Granules (FJG) are a traditional Chinese used in the treatment of diabetes mellitus. However, the antidiabetic mechanism of FJG is not clear. Objective: This study evaluates and determines the antidiabetic mechanism of FJG using a Zucker diabetic fatty (ZDF) rat model. Materials and methods: ZDF (fa/fa) rats were divided into four groups (n = 6): diabetes mellitus (DM), metformin (Met, 0.134 g/kg b.w./day), FJG (0.64 g/kg b.w./day), and combination (Com, 0.134 g/kg b.w./day of Met and 0.64 g/kg b.w./day of FJG). Six ZDF (fa/+) rats served as a normal control. After 6 weeks, biochemical parameters gene and protein expression were detected. Results: The FBG, bodyweight, triglyceride (TG), total cholesterol (TC), free fatty acid (FFA), insulin levels, and HOMA-IR were lower in the FJG than in the DM group (p < 0.05, p < 0.01). In an oral glucose tolerance test, the AUC in the FJG group was significantly lower (p < 0.01). The levels of superoxide dismutase and catalase were higher in the FJG than in the DM group (p < 0.01); the malondialdehyde content and TNF-α were significantly decreased in the FJG group (p < 0.01). FJG increased the mRNA expression of IR and GLUT4 significantly (p < 0.05, p < 0.01). The protein levels of IR, p-IRS1 tyr989, m-PI3Kp85, p-Akt and GLUT4 were increased in the FJG (p < 0.05, p < 0.01), but the protein levels of p-IRS1 ser1101/612/307 were significantly decreased in the JG group (p < 0.01). Discussion and conclusions: The antidiabetic mechanism of FJG may be related to regulation of the insulin-signaling pathway in skeletal muscle. These aspects require further research.
format article
author Yunsong Cao
Wen Sun
Guangyuan Xu
author_facet Yunsong Cao
Wen Sun
Guangyuan Xu
author_sort Yunsong Cao
title Fuzhu jiangtang granules combined with metformin reduces insulin resistance in skeletal muscle of diabetic rats via PI3K/Akt signaling
title_short Fuzhu jiangtang granules combined with metformin reduces insulin resistance in skeletal muscle of diabetic rats via PI3K/Akt signaling
title_full Fuzhu jiangtang granules combined with metformin reduces insulin resistance in skeletal muscle of diabetic rats via PI3K/Akt signaling
title_fullStr Fuzhu jiangtang granules combined with metformin reduces insulin resistance in skeletal muscle of diabetic rats via PI3K/Akt signaling
title_full_unstemmed Fuzhu jiangtang granules combined with metformin reduces insulin resistance in skeletal muscle of diabetic rats via PI3K/Akt signaling
title_sort fuzhu jiangtang granules combined with metformin reduces insulin resistance in skeletal muscle of diabetic rats via pi3k/akt signaling
publisher Taylor & Francis Group
publishDate 2019
url https://doaj.org/article/648608daf3464d95a19ce64301bfba19
work_keys_str_mv AT yunsongcao fuzhujiangtanggranulescombinedwithmetforminreducesinsulinresistanceinskeletalmuscleofdiabeticratsviapi3kaktsignaling
AT wensun fuzhujiangtanggranulescombinedwithmetforminreducesinsulinresistanceinskeletalmuscleofdiabeticratsviapi3kaktsignaling
AT guangyuanxu fuzhujiangtanggranulescombinedwithmetforminreducesinsulinresistanceinskeletalmuscleofdiabeticratsviapi3kaktsignaling
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