PMID- 17369104 OWN - NLM STAT- MEDLINE DCOM- 20070827 LR - 20131121 IS - 1566-0702 (Print) IS - 1566-0702 (Linking) VI - 134 IP - 1-2 DP - 2007 Jul 31 TI - D-beta-hydroxybutyrate inhibits the apoptosis of PC12 cells induced by 6-OHDA in relation to up-regulating the ratio of Bcl-2/Bax mRNA. PG - 38-44 AB - D-beta-hydroxybutyrate (DbetaHB) is a predominant member of ketone bodies produced by hepatocytes and, to a lesser extent, by astrocytes. It is an alternative source of energy in the brain when glucose supply is depleted such as during starvation. It has been reported that ketone bodies could protect dopaminergic culture. However, the biological function of DbetaHB in Parkinson disease (PD) is still unclear. In the present work, we investigated the role of DbetaHB in protecting rat pheochromocytoma (PC12) cells from apoptosis induced by 6-Hydroxydopamine (6-OHDA). DbetaHB rescued PC12 cells from apoptotic death induced by 6-OHDA by MTT assay, acridine orange (AO) staining, terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) staining and the activity of caspase-3. DbetaHB prevented the decrease of cell viability and the increase of caspase-3 activity induced by 6-OHDA in a dose-dependent manner in PC12 cells. AO and TUNEL staining showed that DbetaHB prevented the apoptosis of PC12 cells induced by 6-OHDA. The ratio of Bcl-2/Bax at mRNA levels, which regulates the apoptosis of PC12 cells when exposed to 6-OHDA, increased when DbetaHB was preincubated. The data showed that DbetaHB inhibited the apoptosis of PC12 cells induced by 6-OHDA in relation to up-regulating the ratio of Bcl-2/Bax mRNA. FAU - Cheng, Baohua AU - Cheng B AD - Shandong University, Jinan, China. chengbh1979@163.com FAU - Yang, Xinxin AU - Yang X FAU - Hou, Zhongyu AU - Hou Z FAU - Lin, Xiangtao AU - Lin X FAU - Meng, Haiwei AU - Meng H FAU - Li, Zhenping AU - Li Z FAU - Liu, Shuwei AU - Liu S LA - eng PT - Journal Article DEP - 20070321 PL - Netherlands TA - Auton Neurosci JT - Autonomic neuroscience : basic & clinical JID - 100909359 RN - 0 (Bax protein, rat) RN - 0 (RNA, Messenger) RN - 0 (Sympatholytics) RN - 0 (bcl-2-Associated X Protein) RN - 8HW4YBZ748 (Oxidopamine) RN - EC 3.4.22.- (Caspase 3) RN - TZP1275679 (3-Hydroxybutyric Acid) SB - IM MH - 3-Hydroxybutyric Acid/*pharmacology MH - Animals MH - Apoptosis/*drug effects/physiology MH - Caspase 3/metabolism MH - Cell Survival/drug effects/physiology MH - Drug Interactions MH - Gene Expression Regulation/drug effects MH - Microscopy/methods MH - Neurons/cytology/*drug effects/physiology MH - Oxidopamine/*pharmacology MH - PC12 Cells MH - RNA, Messenger/metabolism MH - Rats MH - Sympatholytics/*pharmacology MH - Up-Regulation/drug effects/physiology MH - bcl-2-Associated X Protein/*genetics EDAT- 2007/03/21 09:00 MHDA- 2007/08/28 09:00 CRDT- 2007/03/21 09:00 PHST- 2006/11/20 00:00 [received] PHST- 2007/02/06 00:00 [revised] PHST- 2007/02/06 00:00 [accepted] PHST- 2007/03/21 09:00 [pubmed] PHST- 2007/08/28 09:00 [medline] PHST- 2007/03/21 09:00 [entrez] AID - S1566-0702(07)00043-4 [pii] AID - 10.1016/j.autneu.2007.02.002 [doi] PST - ppublish SO - Auton Neurosci. 2007 Jul 31;134(1-2):38-44. doi: 10.1016/j.autneu.2007.02.002. Epub 2007 Mar 21.