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C H A P T E R<br />

15<br />

Neuro<strong>trans</strong>mitters<br />

Richard J. Martin 1 , Jennifer Purcell 2 , Tim Day 1 and Alan P. Robertson 1<br />

1 Department of Biomedical Sciences, College of Veterinary Medicine,<br />

Iowa State University, Ames, IA 50011, USA; and<br />

2 Department of Preclinical Veterinary Sciences, R.(D.)S.V.S., Summerhall,<br />

University of Edinburgh, Edinburgh EH9 IQH, UK<br />

NEUROTRANSMITTERS IN<br />

NEMATODES<br />

Introduction<br />

The study of neuro<strong>trans</strong>mitters in parasitic<br />

nematodes has been encouraged by the need<br />

for the development of novel anti-nematodal<br />

drugs and a requirement for an understanding<br />

of the mode of action of these drugs. The<br />

study of neuro<strong>trans</strong>mitters and the study of<br />

anthelmintics are therefore interconnected.<br />

An early illustration of this connection was<br />

the discovery of the action of the inhibitory<br />

neuro<strong>trans</strong>mitter GABA and the effect of the<br />

anthelmintic piperazine in Ascaris.<br />

We know now that the anthelmintics levamisole,<br />

pyrantel, piperazine and ivermectin<br />

(Figures 15.1, 15.2 and 15.3) mimic the effect<br />

of neuro<strong>trans</strong>mitters that open membrane ion<br />

channels of nematodes (Table 15.1). Piperazine<br />

mimics the effect of the inhibitory <strong>trans</strong>mitter<br />

O<br />

O<br />

CH 3<br />

C<br />

N Acetylcholine<br />

CH 3<br />

CH 3<br />

CH 3<br />

S<br />

S<br />

N<br />

N<br />

N<br />

N<br />

N<br />

CH 3<br />

Levamisole<br />

Pyrantel<br />

FIGURE 15.1 Chemical structures of acetylcholine<br />

and the nicotinic anthelmintics, levamisole and<br />

pyrantel. Note that levamisole is the L-isomer of the<br />

D-L mixture, tetramisole.<br />

Molecular Medical Parasitology<br />

ISBN 0–12–473346–8<br />

359<br />

Copyright © 2003 Elsevier Science Ltd.<br />

All rights of reproduction in any form reserved.

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