Pathak Neelima, Khandelwal Shashi
Industrial Toxicology Research Centre, Mahatma Gandhi Marg, P.Box 80, Lucknow - 226001, India.
Eur J Pharmacol. 2007 Dec 8;576(1-3):160-70. doi: 10.1016/j.ejphar.2007.07.033. Epub 2007 Jul 25.
Piper longum Linn. and Piper nigrum Linn. are conventionally used as immuno-enhancers in Indian system of traditional medicine. The underlying mechanism remains unknown. The present study was therefore, undertaken to delineate the role of piperine (major alkaloid) in cadmium (Cd) induced immuno-compromised murine splenocytes. The various biological determinants such as oxidative stress markers (reactive oxygen species and GSH), Bcl-2 protein expression, mitochondrial membrane potential, caspase-3 activity, DNA damage, splenic B and T cell population, blastogenesis and cytokines (Interleukin-2 and gamma-Interferon) were measured to ascertain its cell protective potential. Cadmium induces apoptosis at 6 h onwards. The oxidative stress markers markedly alter prior to a decline in mitochondrial membrane potential, caspase-3 activation and DNA degradation The splenic cell population was observed to change only at 18 h and the release of two cytokines was affected at 72 h. Addition of piperine in various concentrations (1, 10 and 50 microg/ml) ameliorated the above events. The highest dose of piperine could completely abrogate the toxic manifestations of cadmium and the splenic cells behaved similar to control cells. The reported free radical scavenging property of piperine and its antioxidant potential could be responsible for the modulation of intracellular oxidative stress signals. These in turn appear to mitigate the apoptotic pathway and other cellular responses altered by cadmium. The findings strongly indicate the anti-oxidative, anti-apoptotic and chemo-protective ability of piperine in blastogenesis, cytokine release and restoration of splenic cell population and is suggestive of its therapeutic usefulness in immuno-compromised situations.
长蒌叶胡椒和黑胡椒在印度传统医学体系中传统上被用作免疫增强剂。其潜在机制尚不清楚。因此,本研究旨在阐明胡椒碱(主要生物碱)在镉诱导的免疫受损小鼠脾细胞中的作用。测量了各种生物学指标,如氧化应激标志物(活性氧和谷胱甘肽)、Bcl-2蛋白表达、线粒体膜电位、半胱天冬酶-3活性、DNA损伤、脾脏B细胞和T细胞群体、细胞增殖以及细胞因子(白细胞介素-2和γ-干扰素),以确定其细胞保护潜力。镉在6小时后开始诱导细胞凋亡。在线粒体膜电位下降、半胱天冬酶-3激活和DNA降解之前,氧化应激标志物明显改变。脾脏细胞群体仅在18小时时观察到变化,两种细胞因子的释放在72小时时受到影响。添加不同浓度(1、10和50微克/毫升)的胡椒碱可改善上述情况。最高剂量的胡椒碱可完全消除镉的毒性表现,脾脏细胞的行为与对照细胞相似。报道的胡椒碱的自由基清除特性及其抗氧化潜力可能是调节细胞内氧化应激信号的原因。这些反过来似乎减轻了镉改变的凋亡途径和其他细胞反应。研究结果强烈表明胡椒碱在细胞增殖、细胞因子释放和脾脏细胞群体恢复方面具有抗氧化、抗凋亡和化学保护能力,提示其在免疫受损情况下具有治疗作用。