Impact of L-Arginine on diabetes-induced neuropathy and myopathy: Roles of PAI-1, Irisin, oxidative stress, NF-κβ, autophagy and microRNA-29a

T2DM is a chronic disorder with progressive neuromuscular alterations. L-arginine (ARG) is the most common semi-essential amino acid having several metabolic functions. to investigate the impact of L-arginine in combating diabetic-induced neuromyopathy and its possible mechanisms. 24 rats were divid...

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Published inTissue & cell Vol. 87; p. 102342
Main Authors Galal, Heba M., Abdelhafez, Alaa T., Sayed, Manal M., Gomaa, Walaa M.S., Tohamy, Tohamy Anwar, Gomaa, Asmaa M.S., El-Metwally, Tarek H.
Format Journal Article
LanguageEnglish
Published Scotland Elsevier Ltd 01.04.2024
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Summary:T2DM is a chronic disorder with progressive neuromuscular alterations. L-arginine (ARG) is the most common semi-essential amino acid having several metabolic functions. to investigate the impact of L-arginine in combating diabetic-induced neuromyopathy and its possible mechanisms. 24 rats were divided into CON, CON+ARG, DC, DC+ARG. Behavioral tests, Body weight (BW), fasting blood glucose (FBG), insulin, total antioxidant capacity (TAC), malondialdehyde (MDA), plasminogen activator inhibitor-1 (PAI-1), and irisin were done. Creatine kinase-MM (CK-MM), interleukin 4 (IL-4), interleukin 6 (IL-6), TAC, MDA, expression of microRNA-29a mRNA & light chain 3 protein were determined in muscle. Histological and NF-κβ immunohistochemical expression in muscle and nerve were assessed. ARG supplementation to diabetic rats improved altered behavior, significantly increased BW, insulin, TAC, irisin and Il-4, decreased levels of glucose, microRNA-29a, NF-κβ and LC3 expression, PAI-1, CK-MM and restored the normal histological appearance. ARG supplementation potently alleviated diabetic-induced neuromuscular alterations. [Display omitted] •ARG improved neuromuscular abnormalities in diabetic rats.•ARG reduced inflammation and oxidative stress.•ARG reduced PAI-1, microRNA-29a, NF-κβ and LC3 expression.•ARG increased serum Irisin in diabetic rats.
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ISSN:0040-8166
1532-3072
DOI:10.1016/j.tice.2024.102342