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Sophocarpine Suppresses NF-?B-Mediated Inflammation Both In Vitro and In Vivo and Inhibits Diabetic Cardiomyopathy.


ABSTRACT: Diabetic cardiomyopathy (DCM) is a leading cause of mortality in patients with diabetes. DCM is a leading cause of mortality in patients with diabetes. We used both in vitro and in vivo experiments to investigate the hypothesis that sophocarpine (SPC), a natural quinolizidine alkaloid derived from a Chinese herb, could protect against DCM. We used hyperglycemic myocardial cells and a streptozotocin (STZ)-induced type 1 diabetes mellitus mouse model. SPC protected myocardial cells from hyperglycemia-induced injury by improving mitochondrial function, suppressing inflammation, and inhibiting cardiac apoptosis. The SPC treatment significantly inhibited the activation of nuclear factor kappa-light-chain-enhancer of activated B cells (NF-?B) signaling in high-glucose-stimulated inflammatory responses. Moreover, SPC significantly slowed the development and progression of DCM in STZ-induced diabetic mice. These results show that SPC suppresses NF-?B-mediated inflammation both in vitro and in vivo and may be used to treat DCM.

SUBMITTER: Zou F 

PROVIDER: S-EPMC6836764 | biostudies-literature | 2019

REPOSITORIES: biostudies-literature

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Sophocarpine Suppresses NF-κB-Mediated Inflammation Both <i>In Vitro</i> and <i>In Vivo</i> and Inhibits Diabetic Cardiomyopathy.

Zou Fang F   Wang Ling L   Liu Han H   Wang Wei W   Hu Longlong L   Xiong Xiaoying X   Wu Lijuan L   Shen Yunfeng Y   Yang Renqiang R  

Frontiers in pharmacology 20191031


Diabetic cardiomyopathy (DCM) is a leading cause of mortality in patients with diabetes. DCM is a leading cause of mortality in patients with diabetes. We used both <i>in vitro</i> and <i>in vivo</i> experiments to investigate the hypothesis that sophocarpine (SPC), a natural quinolizidine alkaloid derived from a Chinese herb, could protect against DCM. We used hyperglycemic myocardial cells and a streptozotocin (STZ)-induced type 1 diabetes mellitus mouse model. SPC protected myocardial cells f  ...[more]

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