Polyphenolic Extract of Euphorbia supina Attenuates Manganese-Induced Neurotoxicity by Enhancing Antioxidant Activity through Regulation of ER Stress and ER Stress-Mediated Apoptosis

被引:50
作者
Bahar, Entaz [1 ]
Lee, Geum-Hwa [2 ]
Bhattarai, Kashi Raj [2 ]
Lee, Hwa-Young [2 ]
Choi, Min-Kyung [2 ]
Rashid, Harun-Or [2 ]
Kim, Ji-Ye [3 ,4 ]
Chae, Han-Jung [2 ]
Yoon, Hyonok [1 ]
机构
[1] Gyeongsang Natl Univ, Pharmaceut Sci Res Inst, Coll Pharm, Jinju 52828, Gyeongnam, South Korea
[2] Chonbuk Natl Univ, Sch Med, Dept Pharmacol, Jeonju 54896, South Korea
[3] Severance Hosp, Dept Pathol, Seoul 03722, South Korea
[4] Yonsei Univ, Coll Med, Seoul 03722, South Korea
关键词
manganese; Euphorbia supina; neurotoxicity; antioxidant; neuroprotection; INDUCED OXIDATIVE STRESS; DEVELOPMENTAL TOXICITY; ENDOPLASMIC-RETICULUM; DEATH RECEPTOR; RAT STRIATUM; DNA-DAMAGE; EXPOSURE; MITOCHONDRIAL; CHLORIDE; NRF2/HO-1;
D O I
10.3390/ijms18020300
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Manganese (Mn) is an important trace element present in human body, which acts as an enzyme co-factor or activator in various metabolic reactions. While essential in trace amounts, excess levels of Mn in human brain can produce neurotoxicity, including idiopathic Parkinson's disease (PD)-like extrapyramidal manganism symptoms. This study aimed to investigate the protective role of polyphenolic extract of Euphorbia supina (PPEES) on Mn-induced neurotoxicity and the underlying mechanism in human neuroblastoma SKNMC cells and Sprague-Dawley (SD) male rat brain. PPEES possessed significant amount of total phenolic and flavonoid contents. PPEES also showed significant antioxidant activity in 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging and reducing power capacity (RPC) assays. Our results showed that Mn treatment significantly reduced cell viability and increased lactate dehydrogenase (LDH) level, which was attenuated by PPEES pretreatment at 100 and 200 mu g/mL. Additionally, PPEES pretreatment markedly attenuated Mn-induced antioxidant status alteration by resolving the ROS, MDA and GSH levels and SOD and CAT activities. PPEES pretreatment also significantly attenuated Mn-induced mitochondrial membrane potential (m) and apoptosis. Meanwhile, PPEES pretreatment significantly reversed the Mn-induced alteration in the GRP78, GADD34, XBP-1, CHOP, Bcl-2, Bax and caspase-3 activities. Furthermore, administration of PPEES (100 and 200 mg/kg) to Mn exposed rats showed improvement of histopathological alteration in comparison to Mn-treated rats. Moreover, administration of PPEES to Mn exposed rats showed significant reduction of 8-OHdG and Bax immunoreactivity. The results suggest that PPEES treatment reduces Mn-induced oxidative stress and neuronal cell loss in SKNMC cells and in the rat brain. Therefore, PPEES may be considered as potential treat-ment in Mn-intoxicated patients.
引用
收藏
页数:20
相关论文
共 62 条
[21]
Ganie S, 2012, FREE RADICAL BIO MED, V53, pS106, DOI [10.3967/0895-3988.2013.03.008, 10.1016/j.freeradbiomed.2012.08.222]
[22]
Carcinogenicity, mutagenicity and teratogenicity of manganese compounds [J].
Gerber, GB ;
Léonard, A ;
Hantson, P .
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2002, 42 (01) :25-34
[23]
The road to elucidating the mechanism of manganese-bilirubin-induced cholestasis [J].
Goering, PL .
TOXICOLOGICAL SCIENCES, 2003, 73 (02) :216-219
[24]
Hudnell HK, 1999, NEUROTOXICOLOGY, V20, P379
[25]
CELLULAR MANGANESE UPTAKE BY THE ISOLATED PERFUSED RAT-HEART - A PROBE FOR THE SARCOLEMMA CALCIUM-CHANNEL [J].
HUNTER, DR ;
HAWORTH, RA ;
BERKOFF, HA .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1981, 13 (09) :823-832
[26]
Iregren A, 1999, NEUROTOXICOLOGY, V20, P315
[27]
Cardiovascular safety of MnDPDP and MnCl2 [J].
Jynge, P ;
Brurok, H ;
Asplund, A ;
Towart, R ;
Refsum, H ;
Karlsson, JOG .
ACTA RADIOLOGICA, 1997, 38 (04) :740-749
[28]
Death receptor signals to mitochondria [J].
Khosravi-Far, R ;
Esposti, MD .
CANCER BIOLOGY & THERAPY, 2004, 3 (11) :1051-1057
[29]
Polyphenol mixtures of Euphorbia supina the inhibit invasion and metastasis of highly metastatic breast cancer MDA-MB-231 cells [J].
Ko, Young Shin ;
Lee, Won Sup ;
Joo, Young Nak ;
Choi, Yung Hyun ;
Kim, Gon Sup ;
Jung, Jin-Myung ;
Ryu, Chung Ho ;
Shin, Sung Chul ;
Kim, Hye Jung .
ONCOLOGY REPORTS, 2015, 34 (06) :3035-3042
[30]
Korsmeyer SJ, 1999, CANCER RES, V59, p1693S