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Inhibitors of guanylate cyclase inhibit phototransduction in Limulus ventral photoreceptors

Published online by Cambridge University Press:  11 January 2002

ALEX GARGER
Affiliation:
Department of Biology and Volen Center for Complex Systems, Brandeis University, Waltham
EDWIN A. RICHARD
Affiliation:
Department of Biology and Volen Center for Complex Systems, Brandeis University, Waltham
JOHN E. LISMAN
Affiliation:
Department of Biology and Volen Center for Complex Systems, Brandeis University, Waltham

Abstract

The second messenger systems involved in the final stages of the phototransduction cascade in Limulus photoreceptors remain unclear. Excised patches of transducing membrane contain cGMP-gated channels, suggesting the involvement of cGMP in the excitation process. To further explore this possibility, we tested the effects of inhibitors and agonists of guanylate cyclase. The active site cyclase inhibitors guanosine 5′-tetraphosphate and adenosine 5′-tetraphosphate produced a reversible reduction of the response to light without affecting resting membrane properties. The cyclase inhibitor Rp-GTPαS produced a similar reduction, but the effect was only slightly reversible. The reduction in the response produced by these inhibitors was robust, often producing over a 95% decrease in the amplitude of the light response. Previous work had shown that an end-product cyclase inhibitor, imidodiphosphate, also inhibited the response. The consistent results with four different guanylate cyclase inhibitors strongly support the involvement of this enzyme in the phototransduction cascade. To determine whether the guanylate cyclase involved is the NO-dependent soluble form, we applied inhibitors and activators of the nitric oxide synthase/guanylate cyclase pathway such as L-N5-(1-iminoethyl) ornithine, sodium nitroprusside, and carboxy-PTIO. None of these agents had any substantial effect on phototransduction. Taken together, these results support a role for a particulate guanylate cyclase in Limulus photoreceptor excitation.

Type
Research Article
Copyright
2001 Cambridge University Press

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