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Pesticide residues in food — 2007: Toxicological ... - ipcs inchem

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305<br />

(b)<br />

Potentiation of hexobarbiton sleep<strong>in</strong>g time <strong>in</strong> mice<br />

In six male mice, dimethomorph at a dose of 100 mg/kg bw <strong>in</strong>creased the barbital-<strong>in</strong>duced<br />

mean sleep<strong>in</strong>g time from 187.17 m<strong>in</strong> to 257 m<strong>in</strong>. Accord<strong>in</strong>g to the company, this might be expla<strong>in</strong>ed<br />

by competition of dimethomorph with barbital for metabolism pathways (A<strong>in</strong>sworth & Wright,<br />

1991e).<br />

(c)<br />

Alteration of body temperature <strong>in</strong> mice<br />

In six male mice, dimethomorph at a dose of 100 mg/kg bw did not alter the body temperature<br />

(A<strong>in</strong>sworth & Wright, 1991f).<br />

(d)<br />

Spontaneus motor activity <strong>in</strong> mice<br />

In six male mice, dimethomorph at a dose of 100 mg/kg bw did not statistically significant<br />

<strong>in</strong>crease spontaneous locomotor activity. However, a very slight <strong>in</strong>crease <strong>in</strong> groom<strong>in</strong>g was observed<br />

(A<strong>in</strong>sworth & Wright, 1991g).<br />

(e)<br />

Tail flick test for analgesia<br />

In six male mice, dimethomorph at a dose of 100 mg/kg bw did not change the reaction time<br />

(tail flick<strong>in</strong>g) to pa<strong>in</strong>. Therefore, dimethomorph has no analgesic activity (A<strong>in</strong>sworth & Wright,<br />

1991i).<br />

(f)<br />

Effect on the Irw<strong>in</strong> test <strong>in</strong> mice<br />

In groups of five male and five female mice given dimethomorph at a dose of 30, 100 or<br />

300 mg/kg bw, the results of the Irw<strong>in</strong> test showed very mildly <strong>in</strong>creased <strong>in</strong>cidences of parameters<br />

that suggest a sedative effect (A<strong>in</strong>sworth & Wright, 1991k).<br />

(g)<br />

Charcoal meal transit times <strong>in</strong> the rat small <strong>in</strong>test<strong>in</strong>es<br />

In groups of five male and five female rats given dimethomorph at a dose of 30, 100 or 300 mg/<br />

kg bw, <strong>in</strong>test<strong>in</strong>al motility measured as charcoal-meal transit (migration distance at a certa<strong>in</strong> timepo<strong>in</strong>t<br />

as percentage of the whole length of <strong>in</strong>test<strong>in</strong>e) was not <strong>in</strong>fluenced <strong>in</strong> males but was <strong>in</strong>creased <strong>in</strong><br />

females <strong>in</strong> a dose-related manner (A<strong>in</strong>sworth & Wright, 1991d).<br />

(h)<br />

Effect on motility of uter<strong>in</strong>e smooth muscle <strong>in</strong> rats<br />

Smooth muscles from preparations of rat uterus were reproducibly <strong>in</strong>duced to contract by acetylchol<strong>in</strong>e<br />

and this contraction could be <strong>in</strong>hibited by adrenal<strong>in</strong>e. Dimethomorph at concentrations<br />

of up to 30 μg/ml had no effect greater than that of the vehicle (dimethylformamide) on muscle<br />

contraction and did not <strong>in</strong>terfere with the chol<strong>in</strong>ergic and adrenergic receptor dependant reactions<br />

(A<strong>in</strong>sworth & Wright, 1991j).<br />

(i)<br />

Assessment of potential anti-<strong>in</strong>flammatory activity <strong>in</strong> rats<br />

In groups of eight male and eight female rats given dimethomorph at a dose of 30, 100 or<br />

300 mg/kg bw, the <strong>in</strong>flammation potential of dimethomorph was <strong>in</strong>vestigated by kappa carrageenan<br />

<strong>in</strong>jection <strong>in</strong> the h<strong>in</strong>d paw. Edema formation was <strong>in</strong>hibited at 300 mg/kg bw <strong>in</strong> males (A<strong>in</strong>sworth &<br />

Wright, 1991b).<br />

DIMETHOMORPH 273–315 JMPR <strong>2007</strong>

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