Carnosine Improves Cognitive Impairment Through Promoting SIRT6 Expression and Inhibiting Endoplasmic Reticulum Stress in a Diabetic Encephalopathy Model

التفاصيل البيبلوغرافية
العنوان: Carnosine Improves Cognitive Impairment Through Promoting SIRT6 Expression and Inhibiting Endoplasmic Reticulum Stress in a Diabetic Encephalopathy Model
المؤلفون: Dong Peng, Qing Xia, Li Guan, Hong-Ying Li, Li-Jun Qiao, Yun-Bo Chen, Ye-Feng Cai, Qi Wang, Shi-Jie Zhang
المصدر: Rejuvenation research. 25(2)
سنة النشر: 2022
مصطلحات موضوعية: Aging, Brain Diseases, Mice, Diabetes Mellitus, Type 2, Carnosine, Endoribonucleases, Animals, Sirtuins, Apoptosis, Cognitive Dysfunction, Geriatrics and Gerontology, Protein Serine-Threonine Kinases, Endoplasmic Reticulum Stress
الوصف: Diabetic encephalopathy (DE) is one of complications of diabetes mellitus. Carnosine is a dipeptide composed of β-alanine and l-histidine. Study has shown that carnosine could ameliorate cognitive impairment in animal model with diabetes mellitus. However, the mechanism remains unclear. An animal model of type 2 diabetes (db/db mice) was used in this study. The animals were treated with 0.9% saline or carnosine (100 mg/kg) for 8 weeks. Morris water maze was tested after drug administration. Oxidative stress-related factors malondialdehyde (MDA), superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GSH-PX), and pro-inflammatory factors inducible nitric oxide synthase (iNOS) were measured. Synapse-related protein postsynaptic density 95 (PSD95) and brain-derived neurotrophic factor (BDNF) were detected by western blot. Besides, the expressions of sirtuin 6 (SIRT6), binding immunoglobulin protein (BIP), protein kinase R-like endoplasmic reticulum kinase (PERK), phospho-protein kinase R-like endoplasmic reticulum kinase (P-PERK), inositol-requiring enzyme-1α (IRE1α), phospho-inositol-requiring enzyme-1α (P-IRE1α), activating transcription factor 6 (ATF6), and C/EBP-homologous protein (CHOP) in the hippocampus of the brain were detected. The results showed that treatment with carnosine ameliorated cognitive impairment in db/db mice. Carnosine reduced neuronal oxidative stress damage and iNOS expression in db/db mice. Meanwhile, carnosine relieved neurodegeneration in the hippocampus of db/db mice. Furthermore, carnosine promoted the expression of SIRT6 and reduced the expressions of endoplasmic reticulum (ER)-related factors (BIP, P-PERK, P-IRE1α, ATF6, and CHOP). In conclusion, these data suggested that the protective effect of carnosine against DE might be related to SIRT6/ER stress pathway.
تدمد: 1557-8577
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::507e538d0cb475adbb87febc4b20e57b
https://pubmed.ncbi.nlm.nih.gov/35302398
حقوق: CLOSED
رقم الأكسشن: edsair.doi.dedup.....507e538d0cb475adbb87febc4b20e57b
قاعدة البيانات: OpenAIRE