Department of Physiology, Shandong Provincial Key Laboratory of Pathogenesis and Prevention of Neurological Disorders and State Key Disciplines: Physiology, Medical College of Qingdao University, Qingdao 266071, China
*These authors contributed equally to this work.

Abstract 

Obestatin is an endogenous peptide sharing a precursor with ghrelin. This study aims to investigate whether and how obestatin protects MES23.5 dopaminergic cells against 1-methyl-4-phenylpyridinium (MPP+)-induced neurotoxicity. MES23.5 cells were pretreated with obestatin (10-13–10-6 mol/L) for 20 min prior to incubation with 200 μmol/L MPP+ for 12 or 24 h, or treated with obestatin alone (10-13 to 10-6 mol/L) for 0, 6, 12, and 24 h. The methyl thiazolyl tetrazolium (MTT) assay was used to measure cell viability. Flow cytometry was used to measure the caspase-3 activity and the mitochondrial transmembrane potential. Proliferating cell nuclear antigen (PCNA) protein levels were determined by Western blotting. Obestatin (10-13 to 10-7 mol/L) pretreatment blocked or even reversed the MPP+-induced reduction of viability in MES23.5 cells, but had no effect on MPP+-induced mitochondrial transmembrane potential collapse and caspase-3 activation. When applied alone, obestatin increased viability. Elevated PCNA levels occurred with 10-7, 10-9, 10-11 and 10-13 mol/L obestatin treatment for 12 h. The results suggest that the protective effects of obestatin against MPP+ in MES23.5 cells are due to its proliferation-promoting rather than anti-apoptotic effects.

Keywords

obestatin; MPP+; proliferation; apoptosis; dopaminergic cells

[SpringerLink]