دورية أكاديمية

Carnosol and its analogues attenuate muscle atrophy and fat lipolysis induced by cancer cachexia

التفاصيل البيبلوغرافية
العنوان: Carnosol and its analogues attenuate muscle atrophy and fat lipolysis induced by cancer cachexia
المؤلفون: Shanshan Lu, Yiwei Li, Qiang Shen, Wanli Zhang, Xiaofan Gu, Mingliang Ma, Yiming Li, Liuqiang Zhang, Xuan Liu, Xiongwen Zhang
المصدر: Journal of Cachexia, Sarcopenia and Muscle, Vol 12, Iss 3, Pp 779-795 (2021)
بيانات النشر: Wiley, 2021.
سنة النشر: 2021
المجموعة: LCC:Diseases of the musculoskeletal system
LCC:Human anatomy
مصطلحات موضوعية: Carnosol, Cancer cachexia, Muscle atrophy, Lipolysis, NF‐κB, Diseases of the musculoskeletal system, RC925-935, Human anatomy, QM1-695
الوصف: Abstract Background Cancer cachexia is a multifactorial debilitating syndrome that directly accounts for more than 20% of cancer deaths while there is no effective therapeutic approach for treatment of cancer cachexia. Carnosol (CS) is a bioactive diterpene compound present in Lamiaceae spp., which has been demonstrated to have antioxidant, anti‐inflammatory, and anticancer properties. But its effects on cancer cachexia and the possible mechanism remain a mystery. Methods The in vitro cell models of C2C12 myotube atrophy and 3T3‐L1 mature adipocyte lipolysis were used to check the activities of CS and its synthesized analogues. C26 tumour‐bearing BALB/c mice were applied as the animal model to examine their therapeutic effects on cancer cachexia in vivo. Levels of related signal proteins in both in vitro and in vivo experiments were examined using western blotting to study the possible mechanisms. Results Carnosol and its analogues [dimethyl‐carnosol (DCS) and dimethyl‐carnosol‐D6 (DCSD)] alleviated myotube atrophy of C2C12 myotubes and lipolysis of 3T3‐L1 adipocytes in vitro. Interestingly, CS and its analogues exhibited stronger inhibitive effects on muscle atrophy induced by tumour necrosis factor‐α (TNF‐α) (CS, P
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2190-6009
2190-5991
Relation: https://doaj.org/toc/2190-5991; https://doaj.org/toc/2190-6009
DOI: 10.1002/jcsm.12710
URL الوصول: https://doaj.org/article/ab93173e41974abcb194509e6561ba02
رقم الأكسشن: edsdoj.b93173e41974abcb194509e6561ba02
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:21906009
21905991
DOI:10.1002/jcsm.12710