遗传毒性
聚ADP核糖聚合酶
微核试验
DNA损伤
体内
生物信息学
药理学
聚合酶
化学
体外毒理学
四氧嘧啶
体外
微核
生物化学
生物
DNA
遗传学
毒性
基因
有机化学
糖尿病
内分泌学
作者
Sudatta Dey,Isha Nagpal,Priyanka Sow,Rishita Dey,Arnob Chakrovorty,Banani Bhattacharjee,Saikat Saha,Avishek Majumder,Manindranath Bera,Naidu Subbarao,Sisir Nandi,Sabir Hossen Molla,P. Guptaroy,Suresh K. Abraham,Anisur Rahman Khuda‐Bukhsh,Asmita Samadder
标识
DOI:10.1080/07391102.2023.2246585
摘要
The present study tends to evaluate the possible potential of bio-active Morroniside (MOR), against alloxan (ALX)-induced genotoxicity and hyperglycaemia. In silico prediction revealed the interaction of MOR with Poly (ADP-ribose) polymerase (PARP) protein which corroborated well with experimental in vitro L6 cell line and in vivo mice models. Data revealed the efficacy of MOR in the selective activation of PARP protein and modulating other stress proteins NF-κB, and TNF-α to initiate protective potential against ALX-induced genotoxicity and hyperglycaemia. Further, the strong interaction of MOR with CT-DNA (calf thymus DNA) analyzed through CD spectroscopy, UV-Vis study and ITC data revealed the concerted action of bio-factors involved in inhibiting chromosomal aberration and micronucleus formation associated with DNA damage. Finally, MOR does not play any role in microbial growth inhibition which often occurs due to hyperglycemic dysbiosis. Thus, from the overall findings, we may conclude that MOR could be a potential drug candidate for the therapeutic management of induced-hyperglycaemia and genotoxicity.Communicated by Ramaswamy H. Sarma.
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