Effects of pyrethroid structure on rates of hydrolysis and oxidation by mouse liver microsomal enzymes

Studies on the metabolism rates of 44 pyrethroids and 24 model compounds in mouse liver microsomal systems serve to divide the substrates into three groups based on their ease of hydrolysis and oxidation. Primary alcohol esters of trans-substituted cyclopropanecarboxylic acids are most rapidly metabolized with hydrolysis generally serving as the major component of the total metabolism rate. Although hydrolyzed slowly or not at detectable rates, the primary alcohol cis-substituted cyclopropanecarboxylates, tetramethylcyclopropanecarboxylates, and p-chlorophenyl-α-isopropylacetates are rapidly oxidized. The highly insecticidal α-cyano-3-phenoxybenzyl esters are least susceptible to metabolic attack due to both reduced esterase rates attributable to α substitution in the alcohol moiety and reduced oxidase rates for which no adequate explanation is currently available. Other structural modifications in the acid and alcohol moieties are less important in determining the metabolism rates. The substrate specificities of the microsomal esterases and oxidases are compared with in vivo pyrethroid structure-biodegradability relationships.     

Uptake of pesticides from water and soil by earthworms

The uptake of pesticides by earthworms from aqueous solutions was examined and shown to be a reversible physical process. Measurements of distributions of pesticides between aqueous solutions and worm solids showed that adsorption coefficients were related to octanol-water distribution coefficients, as are soil-water distributions. From these relationships it was calculated that concentration factors of stable chemicals in earthworms from soil should be similar, except for polar substances which penetrate poorly, and be determined mainly by the soil organic matter content. Examination of uptake from soils indicated that the calculated concentration factors are unlikely to be achieved because of slow diffusion of chemicals in soils and because of metabolism in the soil or the worm.     

In vitro metabolism of etrimfos by rat and mouse liver

The in vitro metabolism of etrimfos, O,O-dimethyl-O-(2-ethyl-4-ethoxy-6-pyrimidinyl) phosphorothionate, was studied in rat and mouse liver. The major route of metabolism in rat and mouse liver was via glutathione transferase, and the predominant metabolite was desmethyl etrimfos. The higher toxicity of etrimfos to mice was attributed mainly to lower amounts of reduced glutathione in mouse liver. Thus, the level of reduced glutathione appears to be in part responsible for the selective toxicity. No oxygen analog of etrimfos was found.     

In vitro metabolism of EPN and EPNO by mouse liver

The in vitro metabolism of EPN (O-ethyl O-p-nitrophenyl phenylphosphonothionate) and EPNO (O-ethyl O-p-nitrophenyl phenylphosphonate) in mouse liver was studied. EPNO was metabolized faster than EPN, and the highest metabolic activity was found in the 10,000g supernatant in the presence of both NADPH and glutathione. Liver microsomes in the presence of NADPH metabolize EPN to its oxygen analog, EPNO and p-nitrophenol. With the 100,000g supernatant only slight metabolism of EPN occurred in the presence of GSH. Metabolism of EPNO by liver microsomes increased upon the addition of NADPH. p-Nitrophenol was the only metabolite isolated in the presence of microsomes, whereas, with the addition of NADPH, both p-nitrophenol and desethyl EPNO were formed. Quantitative studies showed that there was little, if any, oxidative dearylation of EPNO by liver microsomes. The 100,000g supernatant was found to actively degrade EPNO, and this increased upon addition of glutathione. The initial rate of p-nitrophenol formation as a result of incubation of EPN and EPNO with liver microsomes was found to be higher with EPN than EPNO.     

Hepatic microsomal oxidative metabolism of pesticides and other xenobiotics in pregnant CD1 mice

Pregnancy-related changes in oxidative metabolism of several xenobiotics including pesticides were examined in the hepatic microsomes of CD₁ mice. The effect of pregnancy on hepatic microsomal cytochrome P-450-catalyzed substrate oxidation was found to be dependent upon the type of reaction examined. Not all substrates undergoing the same reaction showed identical changes during pregnancy. Those enzyme activities which exhibited a decline in specific activity during pregnancy generally exhibited no change in total hepatic capacity. Enzymes posting no change in specific activity throughout gestation generally showed large increases in total hepatic activity. Phorate S-oxidation was catalyzed by both microsomal flavin-containing monooxygenase (MFMO) and cytochrome P-450. Moreover, there was no pregnancy-related change in either MFMO or total enzymatic (MFMO plus cytochrome P-450) phorate S-oxidation.     

合成生物学助力链霉菌天然产物农药创制与产业化

病虫草害防控是国家总体安全建设的重要组成部分。微生物天然产物农药是病虫草害绿色防控体系的重要成员, 在保障国家粮食安全、生态安全和农产品质量安全, 筑牢国家生物安全屏障中具有重要作用。链霉菌以能够产生丰富的次级代谢产物而著称, 是天然产物农药的资源宝库, 也是重要的天然产物药物的工业生产菌。然而, 随着病虫草害抗药性增强, 新发、突发病虫草害增多等问题不断涌现, 以及天然产物研究面临新骨架、高活性化合物发现难度增大, 工业菌株产量提升困难等瓶颈, 链霉菌天然产物农药创制与应用正面临巨大挑战。合成生物学作为一门交叉学科, 突破了生物学研究的传统模式, 为天然产物药物研发提供了新的思路与策略。本文综述了近年来合成生物学在链霉菌研究领域的技术革新, 以及合成生物学在推动链霉菌天然产物资源发现、天然产物高效生物制造等方面的研究进展, 并对合成生物学助力链霉菌天然产物农药的创制与产业化进行了展望。     

Inhibition of microsomal oxidoses from the housefly

The hydroxylation of naphthalene, O-demethylation of p-nitroanisole, and N-demethylation of N,N-dimethyl-p-nitrophenylcarbamate by housefly microsomes were inhibited by CO, sulfhydryl reagents, Cu (II), methylene dioxyphenyl compounds and β-diethylaminoethyldiphenylvaleric acid (SKF 525-A). Kinetic analysis indicates that the inhibitory properties of SKF 525-A and piperonyl butoxide are changed during the incubation period. Bovine serum albumen changes the kinetic constants in a way which suggests binding of an endogenous inhibitor(s). Patterns of inhibition indicate p-nitroanisole oxidation is effected by a system with at least one component distinct from the system which oxidizes naphthalene and N,N-dimethyl-p-nitrophenylcarbamate.     

The in vitro metabolism of azinphosmethyl by mouse liver

The in vitro metabolism of methoxy-¹⁴C- or ³²P-azinphosmethyl by subcellular fractions from mouse liver was studied. The major degradative activity was associated with the microsomal and soluble fractions. Since the microsomal activity required NADPH and was inhibited by carbon monoxide, it is reasonable to assume that the mixed function oxidases were involved. The microsomal system catalyzed the dearylation reaction resulting in the formation of dimethyl phosphorothioic acid and dimethyl phosphoric acid. The system was also responsible for the oxidative desulfuration of azinphosmethyl resulting in the formation of azinphosmethyl oxygen analog.     

Metabolism and toxicity of metribuzin in mouse liver

Metribuzin was hepatotoxic in mice when administered intraperitoneally (ip) at sublethal doses of 150 to 250 mg/kg. Four dose-dependent abnormalities were evident. Histopathological examination revealed a fulminant centrilobular hepatic necrosis. The serum glutamic-pyruvic transaminase (GPT) activity was elevated. The liver glutathione (GSH) content was almost completely depleted. There was extensive covalent binding of radiocarbon from [carbonyl-¹⁴C]metribuzin to liver proteins and also high blood levels of metribuzin fragments. Each of these four effects of metribuzin on the liver or blood was alleviated or blocked in mice pretreated with piperonyl butoxide (PB), which inhibits the cytochrome P-450-dependent monooxygenase. PB also reduced the lethality of metribuzin by three-fold. In contrast, pretreatment with diethyl maleate to suppress the liver GSH content increased the lethality of metribuzin by twofold. The hepatotoxicity and acute lethality of metribuzin were probably due to reactive intermediates which are normally detoxified by GSH conjugation. The principal urinary metabolites of metribuzin in mice and rats are mercapturic acids, which arise via metribuzin sulfoxide or deaminometribuzin sulfoxide reacting with GSH. Sulfoxidation therefore appears to activate metribuzin to an electrophilic metabolite which, in the absence of GSH, binds to tissue proteins producing hepatotoxicity.     

In vitro metabolism and interaction of profenofos by human, mouse and rat liver preparations

Biotransformations of profenofos were studied in vitro. Two metabolites, desthiopropylprofenofos and hydroxyprofenofos, were detected by LC-MS after incubation of profenofos with human liver homogenates and different mammalian liver microsomes. The rank order of desthiopropylprofenofos formation in liver microsomes based on intrinsic clearance (V_max/K_m) was mouse > human > rat, while for profenofos hydroxylation it was mouse > rat > human. In view of the ratio between desthiopropylation and hydroxylation intrinsic clearance rates, human liver microsomes were most active in profenofos bioactivation. The interspecies differences and interindividual variation were within range of the default uncertainty/safety factors for chemical risk assessment. CYP3A4, CYP2B6 and CYP2C19 were identified as profenofos-oxidizing enzymes in human liver on the basis of recombinant expressed enzymes and correlation with CYP model activities. The rank order of CYPs in profenofos activation was CYP3A4 > CYP2B6 > CYP2C19, whereas it was the contrary for profenofos hydroxylation. Profenofos inhibited relatively potently several human liver microsomal activities: the lowest IC₅₀ values were about 3 μM for CYP1A1/2 and CYP2B-associated activities. Profenofos is extensively metabolized by liver microsomal CYP enzymes and its interaction potential with several CYP activities is considerable.     

Host plant induction of microsomal monooxygenase activity in relation to diazinon metabolism and toxicity in larvae of the tobacco budworm Heliothis virescens (F.)

The effect of the wild tomato, Lycopersican hirsutam F. glabratam (accession PI 134417), on susceptibility to and metabolism of diazinon, 0,0-diethyl-0-(2-isopropyl-4-methyl-6-pyrimidinyl) phosphorothioate, in larvae of the tobacco budworm, Heliothis virescans F., was studied. The larvae were over 4-fold more tolerant to diazinon toxicity when fed on leaves of wild tomato than when fed on an artificial diet. Diazinon injected into fifth instar larvae is converted into two chloroform-soluble and five water-soluble metabolites. Degradation of diazinon was faster in larvae fed tomato leaves (88.1%) than in larvae fed on the artificial diet (68.4%). Some oxon (13.0%) was detected in the latter case but none in larvae fed tomato leaves. The major metabolite was hydroxypyrimidine and its formation was higher (73.2%) in larvae fed tomato leaves than in larvae fed the artificial diet (49.2%). In vitro studies revealed that both diazinon and its oxon were metabolized primarily by the microsomal cytochrome P-450-dependent monooxygenase system which was induced 2.5- to 3.7-fold by feeding on tomato leaves. It was concluded that diazinon was degraded in H. virescens larvae through desulfuration, hydroxylation of the ring-alkyl side chain, and oxidative dearylation reactions, all of which were increased by varying amounts after feeding on tomato leaves. Treatment of the larvae with 2-tridecanone, a naturally occurring toxin in tomato leaves, resulted in increased tolerance to diazinon and increased in vitro degradation of diazinon and its oxon, the induction being dependent on the magnitude of 2-tridecanone treatment. The microsomes of tomato fed larvae had a 1.5- to 2.1-fold higher concentration of cytochrome P-450, accompanied by a 1–2 nm shift in the λmax of the cytochrome P-450 carbon monoxide complex.     

植物源农药中生物碱提取和纯化技术进展

生物碱是广泛存在于植物中的碱性含氮化合物,一些生物碱因其具有一定的防治病虫害等作用,成为近年来研究的热点。为了使生物碱提取率和纯度不断提高,生物碱的提取与纯化技术也在不断地改进与发展。本文综述了近年来植物源农药中生物碱在提取和纯化新技术的进展,并分析探讨新技术原理、优缺点以及发展前景。     

Isolation of insect microsomal oxidases by rapid centrifugation

Only about 60% of the total relative gravitational force conventionally used to sediment microsomes is needed to prepare highly active microsomes from the midgut tissues of an insect larva. A rapid preliminary centrifugation for 2 min at 39,000g_max effectively removed contaminating microorganisms, tissue debris, nuclei, and mitochondria. The supernatant was recentrifuged for 20 min to 210,000g to sediment the microsomes. There were no losses of microsomal oxidase activities or degradation of cytochrome P-450 to the inactive form (P-420) resulting from the application of the higher gravitational force. Incorporation of 1 mM EDTA in the buffer and washing the microsomes resulted in an improved yield of the cytochrome compared to that in microsomes prepared in sucrose. Yields of microsomal protein, cytochrome P-450, and NADPH-cytochrome c reductase in the rapidly isolated microsomes were as good as those in conventionally prepared microsomes. The apparent kinetic characteristics of several microsomal oxidation activities and optical difference spectra of Types 1 and 2 ligands were identical in the rapidly and conventionally prepared microsomes. The morphological appearance of the microsomes was examined by electron microscopy. Microsomal pellets prepared by either method were indistinguishable. The rapid procedure saves significant time in microsome preparation and yields microsomal oxidase activities as good or slightly better than those prepared by usual centrifuged procedures.     

糠菌唑在大鼠、小鼠、兔、狗和人肝微粒体中的立体选择性代谢

采用高效液相色谱-串联质谱 (HPLC-MS/MS) 手性色谱柱法定量分析肝微粒体中的糠菌唑,通过密度泛函理论计算光谱与振动圆二色光谱 (VCD) 和红外光谱 (IR) 比对,确定了糠菌唑4种对映体的绝对构型;以大鼠、小鼠、兔、狗和人肝微粒体为模型,研究了糠菌唑的立体选择性降解行为。结果表明:在供试肝微粒体中,4种异构体的降解均遵循一级反应动力学方程,且在人和小鼠肝微粒体中的代谢速率相对较慢。(2S, 4R)-和 (2R, 4S)-糠菌唑在5种供试肝微粒体中的立体选择性趋势一致,而 (2R, 4R)- 和 (2S, 4S)-糠菌唑只在兔肝微粒体中的降解有显著的立体选择性差异,在小鼠肝微粒体中几乎没有立体选择性。酶促反应动力学结果也证实了糠菌唑代谢的立体选择性,并显示 (2R, 4R)- 和 (2S, 4S)-糠菌唑在供试肝微粒体中的酶促反应趋势存在种属差异。     

Oxidation of diazinon and malathion by myeloperoxidase

The aim of the work was to investigate the in vitro oxidation of diazinon and malathion, organophosphorous pesticides (OPs) containing phosphorthioate group, catalyzed by enzyme myeloperoxidase (MPO). The oxidation was performed in the presence of hydrogen peroxide. The products were identified as oxon derivatives (phosphates), where the sulfur atom from thioate group was substituted by an oxygen atom. No hydrolysis products were detected after enzyme - induced oxidation. The oxidation efficiency was controlled using acethylcholinesterase (AChE) bioassay for determination of oxon derivatives concentration. The influence of OPs concentration, incubation time of OPs with MPO, as well as MPO concentration on the yield of oxo forms was investigated. Kinetic constants of MPO in oxidation of malathion and diazinon were estimated. The maximum concentration of oxo forms was achieved after 10 min incubation of OPs in 50 mM phosphate buffer (pH 6.0) with 100 nM MPO.     

In-vitro metabolism of O,O-diethyl S-(N-methylcarbamoylmethyl) phosphorodithioate by mouse liver

The in-vitro metabolism of O,O-diethyl S-(N-methylcarbamoymethyl) phosphorodithioate in mouse liver was studied. The major route of metabolism was via the mixed-function oxidases present in the microsomal fraction, which formed the oxygen analogue, O,O-diethyl hydrogen phosphorothioate and diethyl hydrogen phosphate upon addition of nicotinamide-adenine dinucleotide phosphate (NADPH). In the absence of NADPH, the carboxylic acid analogue (S-carboxymethyl O,O-diethyl phosphorodithioate) was isolated only from the microsomal fraction. Addition of glutathione to the 100 000 g supernatant resulted in no metabolism of the parent compound. However, addition of glutathione to the 10 000 g supernatant resulted in the carboxylic acid formed by amidase activity being further metabolised to O,O-diethyl hydrogen phosphorodithioate by a glutathione-dependent reaction.     

微生物降解农药的研究进展

在农药的微生物降解研究中,分离构建一种由天然微生物构成的复合系,将其应用于被污染的环境是消除农药污染的一个有效方法。本文综述了环境中降解农药的微生物种类、微生物降解农药的机理、在自然条件下影响微生物降解农药的因素及农药微生物降解研究方面的新技术和新方法。