Aresti-Sanz Julia, Schwalbe Markus, Pereira Rob Rodrigues, Permentier Hjalmar, El Aidy Sahar
Host-Microbe Interactions, Groningen Biomolecular Sciences and Biotechnology Institute (GBB), University of Groningen, 9747 AG Groningen, The Netherlands.
Medical Center Kinderplein, 3083 BB Rotterdam, The Netherlands.
Pharmaceuticals (Basel). 2021 Jul 27;14(8):733. doi: 10.3390/ph14080733.
Methylphenidate is one of the most widely used oral treatments for attention-deficit/hyperactivity disorder (ADHD). The drug is mainly absorbed in the small intestine and has low bioavailability. Accordingly, a high interindividual variability in terms of response to the treatment is known among ADHD patients treated with methylphenidate. Nonetheless, very little is known about the factors that influence the drug's absorption and bioavailability. Gut microbiota has been shown to reduce the bioavailability of a wide variety of orally administered drugs. Here, we tested the ability of small intestinal bacteria to metabolize methylphenidate. In silico analysis identified several small intestinal bacteria to harbor homologues of the human carboxylesterase 1 enzyme responsible for the hydrolysis of methylphenidate in the liver into the inactive form, ritalinic acid. Despite our initial results hinting towards possible bacterial hydrolysis of the drug, up to 60% of methylphenidate is spontaneously hydrolyzed in the absence of bacteria and this hydrolysis is pH-dependent. Overall, our results indicate that the stability of methylphenidate is compromised under certain pH conditions in the presence or absence of gut microbiota.
哌甲酯是治疗注意力缺陷多动障碍(ADHD)最广泛使用的口服药物之一。该药物主要在小肠吸收,生物利用度低。因此,在用哌甲酯治疗的ADHD患者中,治疗反应存在很大的个体间差异。然而,关于影响该药物吸收和生物利用度的因素却知之甚少。肠道微生物群已被证明会降低多种口服药物的生物利用度。在此,我们测试了小肠细菌代谢哌甲酯的能力。计算机分析确定了几种小肠细菌含有人类羧酸酯酶1的同源物,该酶负责在肝脏中将哌甲酯水解为无活性形式的利他林酸。尽管我们的初步结果暗示该药物可能被细菌水解,但在没有细菌的情况下,高达60%的哌甲酯会自发水解,且这种水解是pH依赖性的。总体而言,我们的结果表明,无论是否存在肠道微生物群,在特定pH条件下哌甲酯的稳定性都会受到影响。