Nicorandil decreases oxidative stress in slow‐ and fast‐twitch muscle fibers of diabetic rats by improving the glutathione system functioning

Autor: Sergio Márquez-Gamiño, Elizabeth Sánchez-Duarte, Sarai Sánchez-Duarte, Fernando Sotelo-Barroso, Cipriana Caudillo-Cisneros, Erick A. Villicaña-Gómez, Ma. Teresa Melchor-Moreno, Rocío Montoya-Pérez, Karla S. Vera-Delgado
Jazyk: angličtina
Rok vydání: 2021
Předmět:
Male
0301 basic medicine
Basic Science and Research
medicine.medical_specialty
Transcription
Genetic

Endocrinology
Diabetes and Metabolism

Diabetic myopathy
030204 cardiovascular system & hematology
medicine.disease_cause
Streptozocin
Diseases of the endocrine glands. Clinical endocrinology
Diabetes Mellitus
Experimental

Lipid peroxidation
03 medical and health sciences
chemistry.chemical_compound
0302 clinical medicine
Internal medicine
Internal Medicine
medicine
TBARS
Animals
Rats
Wistar

Muscle
Skeletal

Nicorandil
Soleus muscle
business.industry
Insulin tolerance test
Articles
General Medicine
Glutathione
Streptozotocin
RC648-665
Rats
Muscle Fibers
Slow-Twitch

030104 developmental biology
Endocrinology
Gene Expression Regulation
chemistry
Oxidative stress
Muscle Fibers
Fast-Twitch

Original Article
Lipid Peroxidation
business
Oxidation-Reduction
medicine.drug
Zdroj: Journal of Diabetes Investigation, Vol 12, Iss 7, Pp 1152-1161 (2021)
Journal of Diabetes Investigation
ISSN: 2040-1116
2040-1124
Popis: Aims/Introduction Myopathy is a common complication of any diabetes type, consisting in failure to preserve mass and muscular function. Oxidative stress has been considered one of the main causes for this condition. This study aimed to search if Nicorandil, a KATP channel opener, could protect slow‐ and fast‐twitch diabetic rat muscles from oxidative stress, and to unveil its possible mechanisms. Materials and Methods Diabetes was induced in male Wistar rats by applying intraperitoneally streptozotocin (STZ) at 100 mg/kg doses. Nicorandil (3 mg/kg/day) was administered along 4 weeks. An insulin tolerance test and assessment of fasting blood glucose (FBG), TBARS, reduced (GSH), and disulfide (GSSG) glutathione levels, GSH/GSSG ratio, and mRNA expression of glutathione metabolism‐related genes were performed at end of treatment in soleus and gastrocnemius muscles. Results Nicorandil significantly reduced FBG levels and enhanced insulin tolerance in diabetic rats. In gastrocnemius and soleus muscles, Nicorandil attenuated the oxidative stress by decreasing lipid peroxidation (TBARS), increasing total glutathione and modulating GPX1‐mRNA expression in both muscle’s types. Nicorandil also increased GSH and GSH/GSSG ratio and downregulated the GCLC‐ and GSR‐mRNA in gastrocnemius, without significative effect on those enzymes’ mRNA expression in diabetic soleus muscle. Conclusions In diabetic rats, Nicorandil attenuates oxidative stress in slow‐ and fast‐twitch skeletal muscles by improving the glutathione system functioning. The underlying mechanisms for the modulation of glutathione redox state and the transcriptional expression of glutathione metabolism‐related genes seem to be fiber type‐dependent.
Databáze: OpenAIRE