Das M, Mallick B N, Dasgupta S C, Gomes A
Laboratory of Toxinology and Experimental Pharmacodynamics, Department of Physiology, University of Calcutta, 92, A.P.C. Road, Calcutta, India.
Toxicon. 2000 Sep;38(9):1267-81. doi: 10.1016/s0041-0101(99)00229-9.
Bufo melanostictus (common Indian toad) acquire different bioactive substances in their skin during their life-time in wide ecological habitat. Earlier investigation from this laboratory revealed that toad (B. melanostictus) skin extract (TSE) posses different bioactive compounds of different diversity (Das, M., Auddy, B. and Gomes, A., 1996. Pharmacological study of the toad skin extract on experimental animals. Indian J. Pharmacol. 28, 72-76). Among these sleep induction and sleep potentiation indicated the possibility of sleep inducing factor(s) in TSE. One such sleep inducing factor (SIF) was isolated and purified by neutral alumina column chromatography followed by HPLC. Spectroscopy (UV, IR, FAB-MASS) study indicated that the sleep inducing factor was a 880 Dalton conjugated aromatic compound with a hydroxyl and carbonyl functional group. Biological study showed that SIF produced no lethality in male albino mice upto the dose of 8 mg/kg, i.v. Cyproheptadine antagonised SIF induced contraction of isolated smooth muscle indicating histamine/serotonin receptor mediated action of SIF. EEG studies showed that SIF increased sleep and decreased awakening condition of freely moving rats. Biochemical studies showed that SIF produced significant alteration of brain biogenic amine levels, monoamine oxidase (MAO) and tryptophan hydroxylase (TH) activity. This may be the reason of SIF induced sleep, although the SIF induced sleep mechanism needs further detail investigation.
黑眶蟾蜍(印度普通蟾蜍)在其广阔生态栖息地的生命周期中,会在皮肤中积累不同的生物活性物质。本实验室早期的研究表明,蟾蜍(黑眶蟾蜍)皮肤提取物(TSE)含有不同种类的生物活性化合物(Das, M., Auddy, B. 和 Gomes, A., 1996年。蟾蜍皮肤提取物对实验动物的药理学研究。《印度药理学杂志》28卷,第72 - 76页)。其中,睡眠诱导和睡眠增强表明TSE中可能存在睡眠诱导因子。通过中性氧化铝柱色谱法,随后再用高效液相色谱法,分离并纯化了一种这样的睡眠诱导因子(SIF)。光谱学(紫外、红外、快原子轰击质谱)研究表明,该睡眠诱导因子是一种880道尔顿的共轭芳香化合物,带有羟基和羰基官能团。生物学研究表明,静脉注射剂量高达8毫克/千克时,SIF对雄性白化小鼠无致死性。赛庚啶拮抗SIF诱导的离体平滑肌收缩,表明SIF的作用是由组胺/5 - 羟色胺受体介导的。脑电图研究表明,SIF增加了自由活动大鼠的睡眠时间并减少了觉醒时间。生化研究表明,SIF使脑生物胺水平、单胺氧化酶(MAO)和色氨酸羟化酶(TH)活性发生了显著变化。这可能是SIF诱导睡眠的原因,尽管SIF诱导睡眠的机制需要进一步详细研究。