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1.
Thirty-six new nitro-alcohol derivatives were synthesised. Tested in vitro against Helminthosporium sativum, the compounds had high antifungal activities; the EC50 values varied between 10?2 and 10?6 M , and for the majority of the compounds between 10?4 and 10?6 M . The EC50 values were calculated by probit analysis, except for the compounds with low activity, for which the values were estimated. Interesting relationships between the structure and antifungal action of the compounds were established.  相似文献   

2.
Eleven 2-n-alkyl-, ten 2-n-alkyl-3-hydroxy- and ten 2-n-alkyl-2,3-epoxy-3-hydro-1,4-naphthoquinones, together with eighteen 1,4-naphthohydroquinone esters were tested as protectant fungicides against the apple and cucumber powdery mildews (caused by Podosphaera leucotricha and Sphaerotheca fuliginea respectively). In.general the former pathogen was more susceptible to compounds from all four series, the lowest 105ED50(M) being 0.7 for 2-n-octyl-2,3-epoxy-3-hydro-1,4 naphthoquinone.  相似文献   

3.
The effect of some 1,3,5-triazine herbicides, on the rate of oxidative decarboxylation of tryptophan by peroxidase from corn seedlings, varied with the concentration. Atrazine was stimulatory in vivo at 10-6M but not at 108 M or lower, whereas terbutryne was inhibitory at 10-6M but not at 10-8M or below. Prometryne inhibited enzyme activity at 10-6M and stimulated it at 10-10M and at 1012M, while simazine caused stimulation at 10-6M and inhibition at 10?10M and 10?12M. Atraton reduced enzyme activity at 10?6M and 10?8M but had no effect at 10?10M and 10?12M. When peroxidase activity was assayed in acetone-dried powders from seeds, harvested from fields that had received typical atrazine applications, the quantities of tryptophan consumed were significantly less than the quantity determined in the control powder. From the results obtained, by incorporating dealkylated and 2-hydroxy metabolites of atrazine at 10?6M into the culture solutions, it seems possible that the inhibition observed may have been due to the presence of 4-amino-6-ethylamino-1, 3, 5-triazin-2-ol and/or 4, 6-diamino-1, 3, 5-triazin-2-ol residues in seeds from treated plots, even if, in previously reported experiments, analyses had not detected their presence.  相似文献   

4.
A series of 2-alkyl-7, 8-dihydro-3-hydroxynaphtho[1,2-c]chromen-6-ones was synthesised by the condensation of ethyl 3, 4-dihydro-1-oxonaphthalene-2-carboxylate with substituted phenols in the presence of POCl3. The compounds were characterised and tested for their toxicity towards the mycelial growth of seven phytopathogenic fungi in culture. Drechslera oryzae, Rhizoctonia solani and Colletotrichum falcatum exhibited maximum sensitivity to these compounds whereas Macro-phomina phaseolina, Fusarium solani, Alternaria alternata and Pythium aphanidermatum were less sensitive. 2-Ethyl-7, 8-dihydro-3-hydroxy-naphtho[1,2-c]chromen-6-ones possessed greatest toxicity with EC50 values ranging from 0.2 to 2.5 μg ml?1 against all fungi except A. alternata and P. aphanidermatum.  相似文献   

5.
Tepraloxydim [(EZ)‐(RS)‐2‐{1‐[(2E)‐3‐chloroallyloxyimino]propyl}‐3‐hydroxy‐5‐perhydropyran‐4‐ylcyclohex‐2‐en‐1‐one] showed high activity against annual bluegrass (Poa annua L.), which is relatively tolerant to sethoxydim [(±)‐2‐(1‐ethoxyiminobutyl)‐5‐[2‐(ethylthio)propyl]‐3‐hydroxycyclohex‐2‐en‐1‐one]. Absorption and translocation rates of tepraloxydim and sethoxydim were higher in P. annua than in Setaria faberi, but the absorption and translocation patterns of tepraloxydim in the two plants were similar to those of sethoxydim. Metabolic rates of tepraloxydim and sethoxydim in P. annua and S. faberi were found to be similar. The concentration for 50% inhibition (I50) of acetyl‐coenzyme A carboxylase (ACCase) with tepraloxydim was approximately 3 × 10?6 mol L?1 for P. annua and 7 × 10?7 mol L?1 for S. faberi. For sethoxydim, the I50 was found to be 2 × 10?6 mol L?1 with the enzyme of S. faberi, while sethoxydim showed a slight effect on ACCase from P. annua activity, even at 10?4 mol L?1. The strong inhibition of ACCase with tepraloxydim is considered to be the major factor contributing to the high herbicidal activity against P. annua. Measuring the whole plant growth response, the ratio of the tepraloxydim I50 dose of P. annua to that of S. faberi (P/S) was found to be 2.4, while the P/S ratio of sethoxydim and a tepraloxydim analog with a propyl chain at R2 were 56.3 and 73.3, respectively. The herbicidal activity against P. annua was remarkably influenced by the length of the R2 alkyl chain, while the effect on S. faberi was not affected. Acetyl‐coenzyme A carboxylase from P. annua also exhibited a higher resistance to the tepraloxydim analog with a propyl chain than to tepraloxydim. These results suggest that a binding site structure of cyclohexane‐1,3‐diones in the ACCase differs between P. annua and S. faberi.  相似文献   

6.
The effect of nitroxynil, rafoxanide, diamphenethide, oxyclozanide and hexachlorophene on the malate dehydrogenase activity of homogenates of Fasciola hepatica was investigated. The ratio of oxaloacetate reduction to malate oxidation in homogenates of F. hepatica was 6.2:1. Nitroxynil, rafoxanide and diamphenethide had no inhibitory effect on malate dehydrogenase at 10?3 M . Oxyclozanide at 10?3 M inhibited malate oxidation by 100% and oxaloacetate reduction by 81%, while 10?3 M hexachlorophene inhibited activity in both directions by 100%. The inhibition quotient (K1 of bovine liver/Ki of F. hepatica) was 7.8 for oxyclozanide and 5.4 for hexachlorophene. No inhibition was seen with 2,4-dinitrophenol at 10?3 M . Rapid death resulted in vitro with 10?4 M oxyclozanide and 10?5 M hexachlorophene. Oxaloacetate reduction was inhibited 61% and malate oxidation 91% with oxyclozanide and 71 and 100% respectively with hexachlorophene. Slow death was also seen at 10?6 M concentration with both products although there was only 30% inhibition of malate dehydrogenase. Both products act as non-competitive inhibitors of malate dehydrogenase and this inhibition is more marked against the mitochondrial subcellular fraction than the cytoplasmic fraction.  相似文献   

7.
Vetiver (Vetiveria zizanioides Nash) cells derived from an inflorescence were cultured in a modified N6 liquid medium supplemented with 10 µm 2,4‐D and 10 mm proline. Exponentially growing cell suspensions were subcultured with a selection medium containing glufosinate (ammonium dl ‐homoalanin‐4‐yl(methyl)phosphinate). The glufosinate‐resistant cells which can grow in a medium containing 5 × 10?5 M glufosinate was selected by a stepwise selection, and its I50 value was determined to be 4.2 × 10?5 M. The growth of susceptible cells was inhibited by lower concentrations of glufosinate and its I50 value was 2.5 × 10?7 M. This indicated that the selected cells were 170‐fold resistant compared with the susceptible cells. Glutamine synthetase (GS) activity of the resistant cells was twice as high as that of the susceptible cells. The I50 values of glufosinate were 3.2 × 10?5 M and 9.0 × 10?7 M for GS from the resistant and susceptible cells, respectively. The accumulation of ammonia caused by GS inhibition was higher in the susceptible cells. Absorption of [3,4–14C]glufosinate was not significantly different between the resistant and susceptible cells. Both cell types did not metabolize glufosinate. These results suggest that the resistance of the selected vetiver cell suspension to glufosinate is mainly due to increased GS activity and its decreased sensitivity to the herbicide.  相似文献   

8.
The inhibitory activity of commercial and experimental triazole fungicides on the target enzyme, sterol 14α-demethylase (P45014DM), was studied in a cell-free sterol synthesis assay of Botrytis cinerea Pers. ex Fr. In order to assess structure-activity relationships, the inhibitory activities of the compounds on radial growth of the fungus were tested as well. The EC50 values (concentrations of fungicide inhibiting radial growth of B. cinerea on PDA by 50%) of all triazoles tested ranged between 10?8 and 10?5 m. IC50 values (concentrations of fungicide inhibiting incorporation of [2-14C]mevalonate into C4-desmethyl sterols by 50%) generally ranged between 10?9 and 10?7 M and correlated with inhibition of radial mycelial growth. However, differences in IC50 values did not reflect quantitatively the observed differences in EC50 values, since the ratio between EC50 and IC50 increased with decreasing fungitoxicity. For a limited number of compounds the correlation between intrinsic inhibitory activity and fungitoxicity was low. Both in-vitro tests were used to investigate structure-activity relationships for stereoisomers of cyproconazole, SSF-109 and tebucona-zole. Fungitoxicity and the potency to inhibit cell-free C4-desmethyl sterol synthesis correlated for all stereoisomers tested. Mixtures of isomers of tebucona-zole or cyproconazole were slightly less active than the most potent isomer. The high activity of several commercial triazoles in both experiments implies that poor field performance of triazole fungicides against B. cinerea is due neither to insensitivity of the P45014DM nor to low in-vitro sensitivity of the fungus.  相似文献   

9.
Benomyl [methyl 1-(butylcarbamoyl)-benzimidazol-2-ylcarbamate] (350 × 10?6 M) decreased the respiration rate of Fusarium oxysporum conidia by 50% during germination. This inhibition was maintained at least 24 h after the treatment had begun. The treatment did not modify the relation between incubation time and respiration rate. Carbendazim [methyl benzimidazol-2-ylcarbamate], thiabendazole[2-(thiazol-4-yl)benzimidazole], thiophanate [1,2-di-(3-ethoxycarbonyl-2-thioureido)benzene] and thiophanate-methyl [1,2-di-(3-methoxycarbonyl-2-thioureido)benzene] were assayed using isolated mitochondria of Saccharomyces cerevisiae. These four compounds decreased mitochondrial respiration and oxidative phosphorylation rates to different extents when they were applied at a concentration of 250 × 10?6 M . Thiophanate-methyl was the most effective since it completely suppressed the mitochondrial respiratory control at 75 × 10?6 M .  相似文献   

10.
Non-cyclopropane pyrethroid esters of different substituted 2-phenoxy-3-methylbutanoic acids have been synthesised using the three alcohols—3-phenoxybenzyl alcohol, α-cyano-3-phenoxybenzyl alcohol and 3, 4-methylene-dioxybenzyl alcohol. Among the 35 esters synthesised and tested against Culex quinquefasciatus Say, the Bancroftian filariasis vector, for both larvicidal and adulticidal activities, α-cyano-3-phenoxybenzyl 2-(4-fluorophenoxy)-3-methylbu-tanoate, with an LC50 value of 2.5 × 10?3 mg litre?1 for larvicidal activity, and α-cyano-3-phenoxybenzyl-2-(4-chlorophenoxy)-3-methylbutanoate, with an LD50 value of 30 times; 10?4 ug insect?1 for adulticidal activity, were found to be as effective as fenvalerate, a well-known non-cyclopropane pyrethroid ester. Structure-activity studies showed that the insecticidal activity is dependent on the nature and position of the substituent in the phenyl ring of the acid moiety and also on the type of alcohol moiety.  相似文献   

11.
A muscarinic acetylcholine receptor (mAChR) has been demonstrated and partially characterized in larvae of the cattle tick Boophilus microplus. Its properties are compared with mAChR from an epithelial cell line from the dipteran insect Chironomus tentans. Competition studies with cholinergic ligands of different specificity revealed the muscarinic nature of the cholinergic receptors investigated in both species. In homogenates from tick larvae, specific binding sites for [3H]quinuclidinyl benzilate (QNB) with high affinity (1·2±(0·13) nM ; Bmax 22·5 pmol mg protein−1) were detected that do not bind nicotinic compounds specifically. The estimated IC50 values for nicotine, imidacloprid and α-bungarotoxin were all in the mM range. Additionally, with tick larvae, high-affinity nicotinic binding sites were detected with [3H]nicotine which could be displaced by high concentrations of imidacloprid or QNB. The estimated IC50 values for nicotine, α-bungarotoxin, imidacloprid and QNB were 43(±8) nM , 0·8(±0·2) μM , 2·8(±0·6) μM and 78(±1·9) μM , respectively. With homogenates of the non-neuronal insect cell line from C. tentans, only high-affinity binding sites for [3H]QNB were found. Muscarinic antagonists selectively displaced [3H]quinuclidinyl benzilate (QNB) binding to tick larvae homogenates. The mAChR of B. microplus preferred pirenzepine (IC50 2·13(±1·02) μM ) among different subtype-specific mAChR antagonists (4-DAMP had IC50 49·9(±9·13) μM and methoctramine had IC50 121(±14·2) μM ) indicating a type of binding site similar to the vertebrate M1 mAChR subtype. The tick muscarinic receptor seems to be a G-protein-coupled receptor, as concluded from the 4·8-fold reduction in receptor affinity for binding of the muscarinic agonist oxotremorine M upon treatment with the non-hydrolysable GTP-analogue γ-S-GTP. Binding data for the agonists oxotremorine M (IC50 71·3(±19·6) μM ) and carbachol (IC50 253(±87·1) μM ) parallel the biological efficacy of these compounds, in that, while oxotremorine M showed some activity against ticks, carbachol was ineffective.  相似文献   

12.
Fresh rhizomes of Zingiber officinale (ginger), when subjected to steam distillation, yielded ginger oil in which curcumene was found to be the major constituent. The thermally labile zingiberene‐rich fraction was obtained from its diethyl ether extract. Column chromatography of ginger oleoresin furnished a fraction from which [6]‐gingerol was obtained by preparative TLC. Naturally occurring [6]‐dehydroshogaol was synthesised following condensation of dehydrozingerone with hexanal, whereas zingerone and 3‐hydroxy‐1‐(4‐hydroxy‐3‐methoxyphenyl)butane were obtained by hydrogenation of dehydrozingerone with 10% Pd/C. The structures of the compounds were established by 1H NMR, 13C NMR and mass (EI‐MS and ES‐MS) spectral analysis. The test compounds exhibited moderate insect growth regulatory (IGR) and antifeedant activity against Spilosoma obliqua, and significant antifungal activity against Rhizoctonia solani. Among the various compounds, [6]‐dehydroshogaol exhibited maximum IGR activity (EC50 3.55 mg ml ?1) while dehydrozingerone imparted maximum antifungal activity (EC50 86.49 mg litre?1). © 2001 Society of Chemical Industry  相似文献   

13.
No registered fungicide controls Mucor piriformis, a cause of severe postharvest storage rot in pears, but the experimental fungicide RH 886 (active ingredients: 77% 5-chloro-2-methylisothiazol-3-(2H)-one and 23% 2-methylisothiazol-3-(2H)-one) has an ED50 of 23.1 μg ml?1 in 5 min exposure for germination of sporangiospores of M. piriformis and an ED50 of 9.9 μg ml?1 for mycelial growth. Mixing RH 886 into infested, amended soil at 8 mg g?1 soil or mixing copper sulfate into soil at 1 mg g?1 soil prevented sporulation of M. piriformis. Application of RH 886 to pear fruits prior to inoculation, or immersion of fruits in solutions of RH 886 containing sporangiospores of M. piriformis significantly reduced fruit infection.  相似文献   

14.
The effects of two herbicides, glyphosate (as a 359 g litre?1 SL) and hexazinone (as a 50gkg?1 granule) on soil microbial population, carbon dioxide evolution, and in-vitro growth of five species of ectomycorrhizal fungi were investigated. Glyphosate at 0–54 and 3.23 kg a.i. ha?1 and hexazinone at 1. 2 and 8 kg a.i. ha?1 did not reduce soil microbial population or carbon dioxide evolution in the long term (6 months). However, there was a significant short-term (2 months) effect of glyphosate on both fungal and bacterial counts at the 0.54 kg ha?1 treatment. In in-vitro tests, Cenococcum graniforme. Hebeloma crustuliniforme and Laccaria laccata were more susceptible to both herbicides than was Suillus tomentosus. which was, in turn, more susceptible than Paxillus involutus. The growth of all five ectomycorrhizal fungi was significantly reduced when subjected to concentrations above 50 μl formulation litre?1 (glyphosate) or 50 μg formulation litre?1 (hexazinone).  相似文献   

15.
Phenylpyrazoles constitute a newly developed class of chemicals with insecticidal and herbicidal properties. In acute toxicity experiments in rats, near-lethal doses of phenylpyrazoles produce neurotoxic symptoms with an unknown mode of action. We have investigated the effects of two phenylpyrazoles, SLA4722 and SLA4685, in the frog neuromuscular junction and in the clonal muscle cell line BC3H-1. In the frog neuromuscular junction SLA4722 at concentrations ? 10?5 M caused a pronounced increase in the frequency of miniature endplate potentials (MEPPs). SLA4685 caused a similar increase but was less potent. In the clonal muscle cell line BC3H-1, SLA4685 produced a concentration-dependent block of the acetylcholine (ACh) response (IC50 = 2.4(±0.3) × 10?5 M). At 10?6 M a slight potentiating effect of SLA4685 on the ACh response was observed. SLA4722 was less potent in this preparation. The increased transmitter release might, at least partly, be responsible for the excitatory effects of the phenylpyrazoles in intact animals.  相似文献   

16.
Based on our previous finding that PIM (phenyl-imidazolyl-metyra-pon; 2-(1-imidazolyl)-2-methyl-1-phenylpropan-1-one, 1) is a strong inhibitor of ecdysone 20-monooxygenase (IC50 = 7.89 × 10?7 M) from the fleshfly, Neobellieria bullata (Parker) and has also a good toxic action in vivo against this insect, 17 imidazole and 1,2,4-triazole analogues of metyrapone were synthesized and evaluated for their action against N. bullata larvae in terms of toxicity, length of larval development, weight of the puparium as well as special symptoms, i.e. malformations of the anterior and posterior spiracles, and of the mandibles. The introduction of p-methoxy (LC50 = 49 mg kg?1 in diet) or p-chloro (LC50 = 97 mg kg?1) substituents on the benzene ring of PIM resulted in a significant increase in toxicity compared to that of metyrapone (LC50 = 561 mg kg?1) and PIM (LC50 = 148 mg kg?1). The hybridization state of the carbon atom adjacent to the benzene ring was not an important factor for toxicity because the acetoxy derivative ( 13 ) was almost as toxic as PIM. At least one methyl group was required on the carbon atom adjacent to the azole ring to maintain activity, while an ethyl group ( 4 ) enhanced the toxic effect. At the applied doses some compounds including metyrapone itself, extended the duration of the larval development. Only metyrapone and PIM decreased the puparium weight. Several derivatives induced lethal malformations of mandibles as well as the anterior and posterior spiracles.  相似文献   

17.
A series of substituted 4-methylcoumarins was synthesised and the members tested for their toxicity towards mycelial growth of seven phytopathogenic fungi in culture. Rhizoctonia solani, Alternaria alternata and Fusarium solani exhibited maximum sensitivity to these compounds whereas Pythium aphanidermatum, Colletotrichum falcatum, Drechslera oryzae and Macrophomina phaseolina were relatively less sensitive. 6-Ethyl-3-n- propyl-7-hydroxy4-methylcoumarin ( I ) was relatively toxic towards all fungi except C. falcatum, P. aphanidermatum and M. phaseolina. The 6-n-butyl ( III ) and 6-(1, 1, 3, 3-tetramethylbutyl) ( VI ) derivatives were highly toxic to R. solani with EC50, values of lμg ml?1.  相似文献   

18.
Mefenoxam is one of the most commonly used fungicides for managing diseases caused by Phytophthora spp. on ornamentals. The objectives of this study were to determine whether Phytophthora nicotianae, a destructive pathogen of numerous herbaceous annual and perennial plant species in nurseries, has developed resistance to mefenoxam, and to evaluate the fitness of mefenoxam‐resistant isolates. Ninety‐five isolates of P. nicotianae were screened for sensitivity to mefenoxam on 20% clarified V8 agar at 100 a.i. µg mL?1. Twenty‐five isolates were highly resistant to this compound with EC50 values ranging from 235·2 to 466·3 µg mL?1 and four were intermediately resistant with EC50 values ranging from 1·6 to 2·9 µg mL?1. Sixty‐six isolates were sensitive with EC50 values less than 0·04 µg mL?1. Nine resistant and seven sensitive isolates were tested for mefenoxam sensitivity on Pelargonium × hortorum cv. White Orbit. Mefenoxam provided good protection of pelargonium seedlings from colonization by sensitive isolates, but not by any resistant isolates. Four resistant and four sensitive isolates were compared for fitness components and their relative competitive ability on Lupinus Russell Hybrids in the absence of mefenoxam. Resistant isolates outcompeted sensitive ones within 3 to 6 sporulation cycles on lupin seedlings, regardless of their initial proportions in mixed zoospore inoculum. Resistant isolates exhibited greater infection rate and higher sporulation ability than sensitive ones when they were applied separately onto lupins. These results suggest that fungicide resistance may pose a serious challenge to the continued effectiveness of mefenoxam as a control option for nursery growers.  相似文献   

19.
The formation of roots and shoots on root segments of Rubus procerus P.J. Muell was prevented by soaking the segments for 24 h in a 10?4M solution of 2,4,5-T or a 10?5M solution of picloram. Shoot numbers were significantly increased after treatment with 10?9M and 10?10M 2,4,5-T, but picloram did not cause a significant increase in shoot numbers. Measurement of the concentration of 2,4,5-T in the extracambial tissue showed that roots treated with 10?4M 2,4,5-T contained 5× 10?8 mmole 2,4,5-T per mg dry weight, and by extrapolation, roots treated with 10?9M 2,4,5-T contained 2× 10?10 mmole/mg dry weight. Action du 2,4,5-T et du piclorame sur la régénération de la ronce (Rubus procerus P.J. Muell) è partir de fragments de racines La formation de racines et de tiges è partir de fragments de racines dc Ruhus procerus P.J. Muell a été supprimée par trempage des fragmenls pendant 24 heures dans une solution a 10?4M et de 2.4,5-T, ou dans une solution 10?5M de piclorame. Le nombre de pousses s'est accru significativement après traitement avec le 2,4,5.-T è 10?9M et 10?10M, mais le piclorame n'a pas provoqué d'accroissemcnt significatif du nombre de pousses. La mesure de la concentration de 2,4,5-T dans le tissu extra-cambial a montré que les racines trailées avec du 2,4,5-T è 10?4M contenaient 5×10?8 mmole de 2.4,5-T par mg de poids sec et par extrapolation, quc les racines traitées avec du 2,4,5-T k 10?9M devaient contenir 2 × 10?12 mmole/mg de poids sec. Die Wirkiing von 2,4,5-T und Picloram auf den Wuchs der Wurzehegmenten von Bromheeren (Rubus procerus P.J. Muell). Die Bildung von Wurzeln und Sprossen aus Wurzelsegmen-ten von Ruhu.i procerus P.J. Muell wurde durch 24-stündiges Einlegen der Wurzelstücke in 10?4M 2,4,5-T bzw 10?5M Picloram verhindert. Die Anzahl neugebiideter Sprosse wurde nach Einlegen in 10?9M und 10?10M 2,4,5-T, nicht jedoch durch Picloram, signifikant erhöht. Im extracambialen Gewebe von Wurzeln, die mit 10?4M 2,4,5-T behand-elt worden waren, wurden 5×10?8mMol 2,4,5-T je mg Trockengewiclu bestimmt. Durch Extrapolation wurde ermittclt. dass mit 10?9M 2,4,5-T behandelte Wurzeln 2× 10?12mMol/mg Trockengewicht cnthielten.  相似文献   

20.
A study of the toxico‐kinetics, recovery percentage from different substrates, cytotoxicity and role of cytochrome P450 and b5 of liver microsome in the metabolism of deltamethrin were carried out in female black Bengal goat. The ALD50 value of deltamethrin in goat by intravenous route lies between 0.2 and 0.6 mg kg?1. Intravenous disposition kinetics using a dose of 0.2 mg kg?1 showed that the maximum blood concentration of deltamethrin was recorded at 0.5 min, followed by rapid decline, and a minimum concentration was detected at 6 min after administration. The following values were obtained : Vdarea 0.148 (± 0.02) litre kg?1; t1/2 (α) 0.22 (± 0.02) min; t1/2 (β) 2.17 (± 0.37) min; Kel 1.05 (± 0.24) min?1; AUC 4.30(± 0.45) µg min ml?1; ClB 0.05 (± 0.006) litre kg?1 min?1; T～B 1.93 (± 0.58); fc 0.40(± 0.05). After 10 min, liver retained the maximum residue, and heart, adrenal gland, kidney, spleen, fat and brain also held the insecticide; liver, fat, heart and spleen retained residue after 30 min, and bone, liver and fat retained residue after 60 min of intravenous administration. Oral absorption of deltamethrin was poor and inconsistent, and approximately 65% of administered dose was recovered from faeces and gastrointestinal contents. The excretion of deltamethrin through urine was meagre, and only 0.01 and 0.013% of the administered dose was recovered after 3 and 5 days of oral administration respectively. All the tissues retained the residue after 3 days; while fat, rumen, reticulum, omasum, abomasum, large and small intestine and bone retained the residue after 5 days of oral administration; and the percentage recoveries were 1.73 and 0.027 respectively. Deltamethrin reduced the level of cytochrome P450 content of liver microsomal pellet of goat after 5 days of oral administration. Histopathological examination of liver, kidney, heart, spleen brain and lung sections of treated goats did not reveal any pathological changes. © 2001 Society of Chemical Industry  相似文献   

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