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학술논문

Effect of Bromocriptine on 6-Hydroxydopamine-induced Lipid Peroxidation and Cytotoxicity in vitro and in vivo

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영문명
Effect of Bromocriptine on 6-Hydroxydopamine-induced Lipid Peroxidation and Cytotoxicity in vitro and in vivo
발행기관
대한생리학회-대한약리학회
저자명
Yong Sik Kim Sungho Maeng Chan Woong Park
간행물 정보
『The Korean Journal of Physiology & Pharmacology』제2권 제5호, 565~572쪽, 전체 8쪽
주제분류
의약학 > 의학일반
파일형태
PDF
발행일자
1998.01.01
4,000

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영문 초록

The present study was to evaluate the protective effects of bromocriptine, which is known as D2 dopamine receptor agonist and used for the treatment of patients with Parkinson s disease (PD), on 6-hydroxydopamine (6-OHDA)-induced neurotoxicity in vitro and in vivo. Lipid peroxidation product (malondialdehyde; MDA) produced by the administration of 6-OHDA was profoundly reduced following the treatment of bromocriptine in a dose-dependent manner in rabbit brain homogenate. Quinone formation by 6-OHDA autoxidation was also attenuated, and its effect was as potent as other antioxidants. Pretreatment of bromocriptine reduced the cytotoxicity of 6-OHDA on SH-SY5Y neuroblastoma cell lines dose-dependently. The loss of striatal dopamine and its metabolite, DOPAC (dihydroxyphenylacetic acid) as well as increase of MDA production caused by intrastriatal injection of 6-OHDA was significantly recovered following the treatment of bromocriptine. The present study clearly showed that bromocriptine had a protective action against 6-OHDA-induced neurotoxicity. These results suggest that bromocriptine has the antioxidant properties, which could be another advantage for delaying the progress of Parkinson s disease.

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APA

Yong Sik Kim,Sungho Maeng,Chan Woong Park. (1998).Effect of Bromocriptine on 6-Hydroxydopamine-induced Lipid Peroxidation and Cytotoxicity in vitro and in vivo. The Korean Journal of Physiology & Pharmacology, 2 (5), 565-572

MLA

Yong Sik Kim,Sungho Maeng,Chan Woong Park. "Effect of Bromocriptine on 6-Hydroxydopamine-induced Lipid Peroxidation and Cytotoxicity in vitro and in vivo." The Korean Journal of Physiology & Pharmacology, 2.5(1998): 565-572

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