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Prevention of Drug-Induced Programmed andUnprogrammed Cell Death by Citrus Flavonoids

机译:通过柑橘类黄酮预防药物诱导的编程的Andunpramumber细胞死亡

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Cell life and cell death in vivo are delicately balanced andlinked processes dependent upon several "death" or "survival"signals from inside and outside the cell. These signals areregulated by several vital intracellular events associated withDNA, RNA, caspases, proteins, and ions. Drugs and otherchemicals are known to threaten the stability of such keyintracellular molecules by causing ion deregulation, oxidativestress, DNA fragmentation and activation of caspases. Citrusflavonoids, such as hesperidin (HES) and rutin (RUT), areknown to specifically interfere with such deleterious pathways,minimize macromolecular perturbations, and exhibit theirprolific antitoxic properties. This study was designed toinvestigate whether HES and RUT pre-exposures (1.25g/kgorally for 14 days) have the ability to counteract hepatotoxicityand nephrotoxicity induced by toxic doses of acetaminophen(APAP, 500 mg/kg, ip) and diclofenac (DCLF, 200 mg/kg, po)respectively in vivo.
机译:体内细胞寿命和细胞死亡是精致的平衡和链接过程,依赖于来自细胞内外的几个“死亡”或“存活”信号。这些信号通过伴随于DNA,RNA,胱天蛋白酶,蛋白质和离子的几个重要细胞内事件产生的信号。已知药物和其他化学物质通过引起离子放松,氧化,氧化剂,DNA片段化和半胱天冬酶活化来威胁这种关键分子的稳定性。柑橘氟烷类(如Hesperidin(HES)和芦丁(RUT),才知道以特定干扰这种有害途径,最小化大分子扰动,并表现出恒定的抗毒性。本研究设计为hes和车辙预曝光(1.25g / kgorally 14天)的设计能够抵消毒性剂量致乙酰氨基酚(Apap,500 mg / kg,IP)和双氯芬酸(DCLF,200的毒性剂量诱导的肝毒性Mg / kg,po)分别在体内。

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