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Clitocybins, novel isoindolinone free radical scavengers, from mushroom Clitocybe aurantiaca inhibit apoptotic cell death and cellular senescence.
Moon, Eun-Yi; Oh, Jin-Mi; Kim, Young-Hee; Ryoo, In-Ja; Yoo, Ick-Dong.
Afiliação
  • Moon EY; Department of Bioscience and Biotechnology, Sejong University, 98 Kunja-Dong Kwangjin-Gu, Seoul 143-747, Republic of Korea. eunyimoon@sejong.ac.kr
Biol Pharm Bull ; 32(10): 1689-94, 2009 Oct.
Article em En | MEDLINE | ID: mdl-19801829
High concentration of intracellular reactive oxygen species (ROS) plays a role in damaging biological systems. We isolated clitocybin A from the culture broth of Clitocybe aurantiaca and then clitocybin B and C derivatives were synthesized from clitocybin A. IMR-90 lung fibroblast cells were pre-treated or post-treated with clitocybin A, B and C to the addition of 100 muM H(2)O(2). These compounds inhibited the level of intracellular reactive oxygen species (ROS) and H(2)O(2)-induced cell death as judged by hypodiploid cell formation. The inhibitory effect of clitocybins on H(2)O(2)-induced cell death was comparable to that with N-acetylcysteine (NAC), a well-known ROS scavenger. The inhibition of H(2)O(2)-induced cell death by clitocybins was mediated by the reduction of caspase 3 and 9 activation, cytochrome c release from mitochondria and the degradation of IkappaB-alpha and IkappaB-beta, which could be resulted in the prevention of cellular senescence. It suggests that clitocybins are novel compounds scavenging ROS and protect cells from apoptosis and cellular senescence.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Fúngicas / Sequestradores de Radicais Livres / Senescência Celular / Apoptose / Agaricales / Isoindóis Limite: Humans Idioma: En Revista: Biol Pharm Bull Ano de publicação: 2009 Tipo de documento: Article
Buscar no Google
Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Fúngicas / Sequestradores de Radicais Livres / Senescência Celular / Apoptose / Agaricales / Isoindóis Limite: Humans Idioma: En Revista: Biol Pharm Bull Ano de publicação: 2009 Tipo de documento: Article