Methoxol's Impact on the Hepatic Microsomal Mixed Function Oxidase System Induced by Phenobarbital and Pyrene in Rats

Abstract

Insecticides like methomyl (Lannate) are commonly used to keep pests at bay in vineyards. The mixed-function oxidase system undergoes dramatic change after being exposed to methomyl. This research set out to determine if methomyl inhibits phenobarbital-induced CYP 2B1, 2B2, and 3A, as well as benzo[a]pyrene-induced CYP 2D6 (CYP 1A1). There were a total of eight groups, each including six adult male rats. Calcium precipitation was used to separate the microsomes. Extinction coefficients were used to quantify the amounts of the electron transport components cytochrome P450, cytochrome B5, and cytochrome c-reductase. Drug metabolizing enzymes were tested for their efficacy. Mixed function oxidase was significantly elevated in rats when exposed to inducers like phenobarbital and benzo[a]pyrene. Inducer-(Phenobarbital, benzop [a] pyrene) pretreated rats given 4mg/kg methomyl had significantly lower levels of electron transport components and drug-metabolizing enzyme activity compared to inducer treatment alone. The enzymes involved in mixed-function oxidation were likewise affected by methomyl's influence on the induction of phenobarbital. The levels of electron transport components and drug metabolizing enzymes in methomyl-pretreated rats treated with benzo[a]pyrene were much lower than in rats treated with benzo[a]pyrene alone. These findings show that phenobarbital and benzo[a]pyrene increased cytochrome P450 isoform susceptibility to methomyl (CYP 2B1, 2B2, 3A; and CYP 1A1) and the induction pattern of some inducers with respect to CYP 450 isoforms are both modified by methomyl