Serseg Talia, Benarous Khedidja
Laboratoire Des Sciences Fondamentales, Universite Amar Telidji, Laghouat, Algeria.
Departement Des Sciences Naturelles, Ecole Normale Superieure de Laghouat, Laghouat, Algerie.
Endocr Metab Immune Disord Drug Targets. 2018;18(6):602-609. doi: 10.2174/1871530318666180319093342.
Side effects of some drugs may be useful in certain cases. In this work, we studied the inhibitory effects on Lipases of some medications as: Folic Acid which is taken by pregnant women, Colchicine and Febuxostat which is used as treatment of gout disease. These cases are linked to obesity, where women (BMI ≥ 30) have twice higher odds of having an NTDaffected pregnancy than the normal weight women, and the Gout disease frequently occurs in combination of a Metabolic syndrome. The risk of gout increases with the increase of the mass index. In silico studies were aimed to determine the mechanism of inhibition and different interactions for two enzymes: Candida rugosa lipase and human pancreatic lipase.
In the first part of this study, we studied the inhibition activity of these medications on lipase activity of Candida rugosa in vitro. Autodock vina was used for molecular docking with 50 runs and 1000 obtained solutions. The saved interactions were with His449 and Ser209 for the three molecules.
The results show that these drugs have an important inhibition activity with IC50 values 0.64 mg/ml for Folic acid and 0.66 mg/ml for Febuxostat. The results of in silico show competitive, Noncompetitive and uncompetitive inhibition for folic acid, febuxostat and colchicine respectively for two enzymes with different repetition ratios of hydrogen bonds.
These observations support a higher intake of dietary folate, and febuxostat for losing weight to decrease NTD risk and prevent hyperuricemia and recurrent gout attacks.
某些药物的副作用在特定情况下可能有用。在本研究中,我们研究了一些药物对脂肪酶的抑制作用,这些药物包括:孕妇服用的叶酸、用于治疗痛风的秋水仙碱和非布索坦。这些情况与肥胖有关,肥胖女性(BMI≥30)发生神经管缺陷妊娠的几率是正常体重女性的两倍,且痛风疾病常与代谢综合征并发。痛风风险随体重指数增加而升高。计算机模拟研究旨在确定两种酶(皱褶假丝酵母脂肪酶和人胰脂肪酶)的抑制机制和不同相互作用。
在本研究的第一部分,我们在体外研究了这些药物对皱褶假丝酵母脂肪酶活性的抑制作用。使用Autodock vina进行分子对接,运行50次,获得1000个解决方案。这三种分子与His449和Ser209存在保存的相互作用。
结果表明,这些药物具有重要的抑制活性,叶酸的IC50值为0.64mg/ml,非布索坦的IC50值为0.66mg/ml。计算机模拟结果表明,叶酸、非布索坦和秋水仙碱对两种酶分别表现出竞争性、非竞争性和非竞争性抑制作用,氢键重复率不同。
这些观察结果支持增加膳食叶酸摄入量以及使用非布索坦来减肥,以降低神经管缺陷风险并预防高尿酸血症和复发性痛风发作。