Analyzing the responses of saccharin in context with melatonin receptors on the melanophores of the fish Labeo rohita (Ham.).

IF 2.3
M D Mubashshir, Fraz Ahmed, Safia Sumoona, Mohd Ovais
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引用次数: 3

Abstract

The hormone melatonin regulates the biological clock and assist in various other physiologies of vertebrates. Present work is intended to check the affinity of saccharin towards the melatonin receptors and the possible role of saccharin interference in the melatonin physiology. The present in vitro study is based on the working model of isolated scale melanophores in the dorso-lateral region of Labeo rohita. The pigment cells were incubated in the agonist and the antagonists within a limited time frame and subsequently their Melanophore Size Index (MSI) were calculated. The inferences were drafted through the observed signal transduction upshots in pigment translocations within the melanophores. Saccharin, in a wide dose range, has consistently induced a concentration-related aggregation similar to the aggregatory effect as shown by melatonin on the melanophores. Binding of saccharin with the receptors and eliciting its aggregatory effect is partially dependent on the release of neurotransmitters. The aggregatory effects were found to be significantly blocked by luzindole, K185, and prazosin, which are the potent melatonin receptor blockers, at the higher concentrations of saccharin. Hence, all the three subtypes of melatonin receptors viz. MT₁, MT₂, and MT₃ are participating in saccharin-mediated aggregations. Blocking by neomycin shows that Ca²⁺ ions are very crucial in dispensing the aggregatory effect of the sweetener. This research demands that an intensive and careful thorough study should be made about saccharin, specifically its effects upon melatonin physiology, before its unwarranted use as the food ingredients for human use.

分析糖精与褪黑激素受体对鱼黑素细胞的反应。
褪黑激素调节生物钟,并协助脊椎动物的各种其他生理机能。本研究旨在探讨糖精对褪黑激素受体的亲和力,以及糖精干扰褪黑激素生理的可能作用。本体外实验是建立在背外侧黑素细胞工作模型的基础上的。将色素细胞在激动剂和拮抗剂中孵育一定时间,然后计算其黑色素细胞大小指数(MSI)。这些推论是通过观察到的黑色素细胞内色素易位的信号转导结果起草的。在大剂量范围内,糖精一直诱导浓度相关的聚集,类似于褪黑素对黑素细胞的聚集效应。糖精与受体结合并激发其聚集作用部分依赖于神经递质的释放。在较高的糖精浓度下,这种聚集效应被有效的褪黑激素受体阻滞剂——卢津多、K185和吡唑嗪显著阻断。因此,褪黑素受体的所有三种亚型,即MT₁、MT₂和MT₃都参与了糖精介导的聚集。新霉素的阻断表明,Ca 2 +离子在分配甜味剂的聚集效应中是非常关键的。这项研究要求对糖精,特别是其对褪黑激素生理的影响进行深入细致的研究,然后再将其毫无根据地用作人类使用的食品成分。
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