Ontology highlight
ABSTRACT: Methods
All rats were randomly divided into four groups, namely, control, CUMS, CUMS + CUR, and CUMS + CUR + SR18292 (PGC-1α inhibitor). Behavioral tests were conducted to assess the antidepressant-like effects of CUR. The expressions of PGC-1α, estrogen-related receptor alpha (ERRα), FNDC5, and BDNF were determined to investigate the regulatory effects of CUR on the PGC-1α/FNDC5/BDNF pathway. The PGC-1α inhibitor SR18292 was used to explore the role of PGC-1α in the induction of BDNF by CUR.Results
Daily gavage of 100 mg/kg CUR successfully attenuated the abnormal behaviors induced by CUMS and effectively prevented CUMS-induced reduction of PGC-1α, ERRα, FNDC5, and BDNF expressions. CUR also enhanced PGC-1α and ERRα translocation from cytoplasm to nucleus. Furthermore, we found that CUR supplementation effectively promoted neurocyte proliferation and suppressed neuronal apoptosis induced by CUMS. Of note, the PGC-1α inhibitor SR18292 remarkably reversed the beneficial effects of CUR on depressed rats, indicating an important role of PGC-1α in the antidepressant-like effects of CUR.Conclusion
Collectively, our data evaluating the neuroprotective action of CUR in the CUMS rats highlights the involvement of the PGC-1α/FNDC5/BDNF pathway in the antidepressant-like effects of CUR.
SUBMITTER: Wu Y
PROVIDER: S-EPMC8692045 | biostudies-literature | 2021
REPOSITORIES: biostudies-literature
Wu Yanqin Y Sun Fusheng F Guo Yujin Y Zhang Yumao Y Li Li L Dang Ruili R Jiang Pei P
Behavioural neurology 20211214
<h4>Methods</h4>All rats were randomly divided into four groups, namely, control, CUMS, CUMS + CUR, and CUMS + CUR + SR18292 (PGC-1<i>α</i> inhibitor). Behavioral tests were conducted to assess the antidepressant-like effects of CUR. The expressions of PGC-1<i>α</i>, estrogen-related receptor alpha (ERR<i>α</i>), FNDC5, and BDNF were determined to investigate the regulatory effects of CUR on the PGC-1<i>α</i>/FNDC5/BDNF pathway. The PGC-1<i>α</i> inhibitor SR18292 was used to explore the role of ...[more]