PMID- 23073806 OWN - NLM STAT- MEDLINE DCOM- 20140909 LR - 20220726 IS - 1672-0733 (Print) IS - 1672-0733 (Linking) VI - 32 IP - 5 DP - 2012 Oct TI - 1,2,3,4,6-penta-O-galloyl-beta-D-glucose protects PC12 Cells from MPP(+)-mediated cell death by inducing heme oxygenase-1 in an ERK- and Akt-dependent manner. PG - 737-745 LID - 10.1007/s11596-012-1027-1 [doi] AB - This study examined the ability of 1,2,3,4,6-penta-O-galloyl-beta-D-glucose (beta-PGG) to induce the expression of heme oxygenase-1 (HO-1) in the PC12 cells and its regulation in the PC12 cells. One week before treatment with the drug, nerve growth factor (NGF) was added to the cultures at a final concentration of 50 ng/mL to induce neuronal differentiation. After drug treatment, HO-1 gene transcription was analyzed by reverse transcription polymerase chain reaction (RT-PCR). Expression of HO-1 and NF-E2-related factor2 (Nrf2) and activation of extracellular signal-regulated kinase (ERK) and Akt were detected by Western blotting. The viability of the PC12 cells treated with different medicines was examined by MTT assay. The oxidative stress in the PC12 cells was evaluated qualitatively and quantitatively by DCFH-DA. The results showed that beta-PGG up-regulated HO-1 expression and this increased expression provided neuroprotection against MPP(+)-induced oxidative injury. Moreover, beta-PGG induced Nrf2 nuclear translocation, which was found to be upstream of beta-PGG-induced HO-1 expression, and the activation of ERK and Akt, a pathway that is involved in beta-PGG-induced Nrf2 nuclear translocation, HO-1 expression and neuroprotection. In conclusion, beta-PGG up-regulates HO-1 expression by stimulating Nrf2 nuclear translocation in an ERK- and Akt-dependent manner, and HO-1 expression by beta-PGG may provide the PC12 cells with an acquired antioxidant defense capacity to survive the oxidative stress. FAU - Chen, Hong AU - Chen H AD - Department of Neurology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China. FAU - Li, Hongge AU - Li H AD - Department of Neurology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China. FAU - Cao, Fei AU - Cao F AD - Department of Neurology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China. FAU - Zhen, Lan AU - Zhen L AD - Department of Obstetrics and Gynecology, Maternal and Child Health Hospital of Fujian Province, Fuzhou, 350001, China. FAU - Bai, Jing AU - Bai J AD - Department of Neurology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China. FAU - Yuan, Shijin AU - Yuan S AD - Division of Histology and Embryology, Department of Anatomy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China. FAU - Mei, Yuanwu AU - Mei Y AD - Department of Neurology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China. lnlhckao@126.com. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20121018 PL - China TA - J Huazhong Univ Sci Technolog Med Sci JT - Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban JID - 101169627 RN - 0 (1,3-bis(4-hydroxyphenyl)-4-methyl-5-(4-(2-piperidinylethoxy)phenol)-1H-pyrazole) RN - 0 (Hydrolyzable Tannins) RN - 0 (Piperidines) RN - 0 (Pyrazoles) RN - 3UI3K8W93I (pentagalloylglucose) RN - EC 1.14.14.18 (Heme Oxygenase-1) RN - EC 2.7.11.1 (Proto-Oncogene Proteins c-akt) SB - IM MH - Animals MH - Cell Death/*drug effects/genetics MH - Cell Line, Tumor MH - Heme Oxygenase-1/*genetics MH - Hydrolyzable Tannins/*pharmacology MH - MAP Kinase Signaling System/*drug effects/genetics MH - PC12 Cells MH - Piperidines/*adverse effects MH - Proto-Oncogene Proteins c-akt/*genetics MH - Pyrazoles/*adverse effects MH - Rats EDAT- 2012/10/18 06:00 MHDA- 2014/09/10 06:00 CRDT- 2012/10/18 06:00 PHST- 2012/02/21 00:00 [received] PHST- 2012/10/18 06:00 [entrez] PHST- 2012/10/18 06:00 [pubmed] PHST- 2014/09/10 06:00 [medline] AID - 10.1007/s11596-012-1027-1 [pii] AID - 10.1007/s11596-012-1027-1 [doi] PST - ppublish SO - J Huazhong Univ Sci Technolog Med Sci. 2012 Oct;32(5):737-745. doi: 10.1007/s11596-012-1027-1. Epub 2012 Oct 18.