Effects of Hydroxysafflor Yellow A on the PI3K/AKT Pathway and Apoptosis of Pancreatic β-Cells in Type 2 Diabetes Mellitus Rats

Maosheng Lee,1,2 Huilin Li,2 Hengxia Zhao,2 Miao Suo,1,2 Deliang Liu2 1The Fourth Clinical Medical College, Guangzhou University of Chinese Medicine, Guangzhou 510006, People’s Republic of China; 2Department of Endocrinology, Shenzhen Traditional Chinese Medicine Hospital, Shenzhen 518033,...

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Autores principales: Lee M, Li H, Zhao H, Suo M, Liu D
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Publicado: Dove Medical Press 2020
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spelling oai:doaj.org-article:2a64699b5bf147a19d9864c1fe7efd212021-12-02T13:11:16ZEffects of Hydroxysafflor Yellow A on the PI3K/AKT Pathway and Apoptosis of Pancreatic β-Cells in Type 2 Diabetes Mellitus Rats1178-7007https://doaj.org/article/2a64699b5bf147a19d9864c1fe7efd212020-04-01T00:00:00Zhttps://www.dovepress.com/effects-of-hydroxysafflor-yellow-a-on-the-pi3kakt-pathway-and-apoptosi-peer-reviewed-article-DMSOhttps://doaj.org/toc/1178-7007Maosheng Lee,1,2 Huilin Li,2 Hengxia Zhao,2 Miao Suo,1,2 Deliang Liu2 1The Fourth Clinical Medical College, Guangzhou University of Chinese Medicine, Guangzhou 510006, People’s Republic of China; 2Department of Endocrinology, Shenzhen Traditional Chinese Medicine Hospital, Shenzhen 518033, People’s Republic of ChinaCorrespondence: Huilin Li Tel/Fax +86 755-8839368Email sztcmlhl@163.comBackground and Aim: Type 2 diabetes mellitus (T2DM), a complex metabolic disease, has become a major public health issue around the world. Hydroxysafflor yellow A (HSYA) is the major active chemical ingredient of Carthamus tinctorius L. (safflower), which is widely used in patients with cardiovascular and cerebrovascular diseases in China. The aim of this study was to investigate the anti-diabetic effect and potential mechanism of HSYA on the high-fat diet (HFD) and streptozotocin (STZ-)-induced T2DM rats.Materials and Methods: T2DM rats were induced by feeding HFD (60% fat) for four weeks followed by intraperitoneal injection of a low dose of streptozocin (35mg/kg). The T2DM rats were treated with HSYA (120mg/kg) or metformin (90mg/kg) for eight weeks. Biochemical analysis, histological analysis and Western blot analysis were conducted after 8 weeks of intervention.Results: The treatment with HSYA evidently reduced fasting-blood glucose and insulin resistance in T2DM rats, indicated by results from fasting-blood glucose, oral glucose tolerance test, fasting insulin levels and histology of pancreas islets. The Western blot results revealed that HSYA reversed the down-regulation of PI3K and AKT in liver. The TUNEL assay analysis of pancreatic tissue showed that HSYA could inhibit the apoptosis of pancreatic β-cells to a certain extent. Moreover, HSYA-treatment increased the levels of glycogen synthase and hepatic glycogen and improved lipid metabolism by reducing the triglyceride, total and low-density lipoprotein cholesterol levels, even though it did not change the rats’ body weights.Conclusion: The results of this study suggested that HSYA could promote PI3K/Akt activation and inhibit the apoptosis of pancreatic β-cells directly or indirectly, which might be the underlying mechanisms in HSYA to improve insulin resistance and regulate glycolipid metabolism in T2DM rats.Keywords: hydroxysafflor yellow A, insulin resistance, PI3K/AKT pathway, apoptosis, type 2 diabetes mellitus, traditional Chinese medicineLee MLi HZhao HSuo MLiu DDove Medical Pressarticlehydroxysafflor yellow ainsulin resistancepi3k/akt pathwayapoptosistype 2 diabetes mellitustraditional chinese medicineSpecialties of internal medicineRC581-951ENDiabetes, Metabolic Syndrome and Obesity: Targets and Therapy, Vol Volume 13, Pp 1097-1107 (2020)
institution DOAJ
collection DOAJ
language EN
topic hydroxysafflor yellow a
insulin resistance
pi3k/akt pathway
apoptosis
type 2 diabetes mellitus
traditional chinese medicine
Specialties of internal medicine
RC581-951
spellingShingle hydroxysafflor yellow a
insulin resistance
pi3k/akt pathway
apoptosis
type 2 diabetes mellitus
traditional chinese medicine
Specialties of internal medicine
RC581-951
Lee M
Li H
Zhao H
Suo M
Liu D
Effects of Hydroxysafflor Yellow A on the PI3K/AKT Pathway and Apoptosis of Pancreatic β-Cells in Type 2 Diabetes Mellitus Rats
description Maosheng Lee,1,2 Huilin Li,2 Hengxia Zhao,2 Miao Suo,1,2 Deliang Liu2 1The Fourth Clinical Medical College, Guangzhou University of Chinese Medicine, Guangzhou 510006, People’s Republic of China; 2Department of Endocrinology, Shenzhen Traditional Chinese Medicine Hospital, Shenzhen 518033, People’s Republic of ChinaCorrespondence: Huilin Li Tel/Fax +86 755-8839368Email sztcmlhl@163.comBackground and Aim: Type 2 diabetes mellitus (T2DM), a complex metabolic disease, has become a major public health issue around the world. Hydroxysafflor yellow A (HSYA) is the major active chemical ingredient of Carthamus tinctorius L. (safflower), which is widely used in patients with cardiovascular and cerebrovascular diseases in China. The aim of this study was to investigate the anti-diabetic effect and potential mechanism of HSYA on the high-fat diet (HFD) and streptozotocin (STZ-)-induced T2DM rats.Materials and Methods: T2DM rats were induced by feeding HFD (60% fat) for four weeks followed by intraperitoneal injection of a low dose of streptozocin (35mg/kg). The T2DM rats were treated with HSYA (120mg/kg) or metformin (90mg/kg) for eight weeks. Biochemical analysis, histological analysis and Western blot analysis were conducted after 8 weeks of intervention.Results: The treatment with HSYA evidently reduced fasting-blood glucose and insulin resistance in T2DM rats, indicated by results from fasting-blood glucose, oral glucose tolerance test, fasting insulin levels and histology of pancreas islets. The Western blot results revealed that HSYA reversed the down-regulation of PI3K and AKT in liver. The TUNEL assay analysis of pancreatic tissue showed that HSYA could inhibit the apoptosis of pancreatic β-cells to a certain extent. Moreover, HSYA-treatment increased the levels of glycogen synthase and hepatic glycogen and improved lipid metabolism by reducing the triglyceride, total and low-density lipoprotein cholesterol levels, even though it did not change the rats’ body weights.Conclusion: The results of this study suggested that HSYA could promote PI3K/Akt activation and inhibit the apoptosis of pancreatic β-cells directly or indirectly, which might be the underlying mechanisms in HSYA to improve insulin resistance and regulate glycolipid metabolism in T2DM rats.Keywords: hydroxysafflor yellow A, insulin resistance, PI3K/AKT pathway, apoptosis, type 2 diabetes mellitus, traditional Chinese medicine
format article
author Lee M
Li H
Zhao H
Suo M
Liu D
author_facet Lee M
Li H
Zhao H
Suo M
Liu D
author_sort Lee M
title Effects of Hydroxysafflor Yellow A on the PI3K/AKT Pathway and Apoptosis of Pancreatic β-Cells in Type 2 Diabetes Mellitus Rats
title_short Effects of Hydroxysafflor Yellow A on the PI3K/AKT Pathway and Apoptosis of Pancreatic β-Cells in Type 2 Diabetes Mellitus Rats
title_full Effects of Hydroxysafflor Yellow A on the PI3K/AKT Pathway and Apoptosis of Pancreatic β-Cells in Type 2 Diabetes Mellitus Rats
title_fullStr Effects of Hydroxysafflor Yellow A on the PI3K/AKT Pathway and Apoptosis of Pancreatic β-Cells in Type 2 Diabetes Mellitus Rats
title_full_unstemmed Effects of Hydroxysafflor Yellow A on the PI3K/AKT Pathway and Apoptosis of Pancreatic β-Cells in Type 2 Diabetes Mellitus Rats
title_sort effects of hydroxysafflor yellow a on the pi3k/akt pathway and apoptosis of pancreatic β-cells in type 2 diabetes mellitus rats
publisher Dove Medical Press
publishDate 2020
url https://doaj.org/article/2a64699b5bf147a19d9864c1fe7efd21
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