Anti-diuresis in the blood-feeding insect Rhodnius prolixus Stål: antagonistic actions of cAMP and cGMP and the role of organic acid transport

• Published in: Journal of insect physiology Vol. 44; no. 7; pp. 561 - 568
• Main Authors: Quinlan, Michael C, O'Donnell, Michael J
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 01.07.1998
• Subjects: anti-diuresis; cAMP; cGMP; Malpighian tubule; secretion; cGMP; secretion; Malpighian tubule; cAMP; anti-diuresis
• ISSN: 0022-1910; 1879-1611
• DOI: 10.1016/S0022-1910(98)00047-X

Secretion of primary urine by upper Malpighian tubules of the blood-sucking insect Rhodnius prolixus has recently been shown to be inhibited by cyclic GMP (cGMP). In the present work, we have demonstrated that cGMP has effects antagonistic to those of cAMP in Rhodnius tubules and have further characterized the effects of cGMP on tubular secretion. Cyclic GMP inhibited secretion at all concentrations from 5×10 −6 to 10 −3 M, though this inhibition was partially or wholly reversed by large (2 mM) doses of cAMP. While sub-maximal concentrations of cGMP did not significantly alter [K +] and [Na +] of secreted fluid, high external [cGMP] reduced secretion to minimal levels and caused [K +] and [Na +] to approach pre-stimulation levels. Cyclic GMP does not appear to affect the permeability of the lower Malpighian tubule to water. Both cAMP and cGMP likely enter tubule cells by way of an organic acid transporter whose activity is induced by feeding. Sensitivity of the tubules to exogenous cGMP and cAMP, which is assumed to be a function of transport activity, reaches a peak ≈5 days after the blood meal and declines rapidly thereafter. Transport of anions into upper tubules involves at least two different transporters: one for acylamides (e.g., p-aminohippuric acid) and another for sulphonates (e.g., amaranth, phenol red). Amaranth and phenol red blocked the actions of both cGMP and cAMP, whereas p-aminohippuric acid was without effect. This suggests that cyclic nucleotides enter by way of the sulphonate transporter.