Journal of Experimental Biology · 1994 · 223 citations · 17 references
Protein SecretionFluid SecretionCellular PhysiologyIntegrative PhysiologyMembrane TransportPlant AlkaloidsSecretory PathwayOsmoregulationNovel PhenotypeMolecular PhysiologyOsmotic StressBiochemistrySodium HomeostasisDevelopmental GeneticsMedicineIon ChannelsMorphogenesisMembrane BiologyNervous SystemPotassium HomeostasisBiologyPattern FormationDevelopmental BiologyNatural SciencesPhysiologyInsect RenalEvolutionary Developmental BiologyMalpighianc TubulesComparative Physiology
ABSTRACT The insect renal (Malpighian) tubule has long been a model system for the study of fluid secretion and its neurohormonal control (Maddrell, 1981; Maddrell and O’Donnell, 1992). Classical physiology suggests a model for tubular secretion of iso-osmotic fluid in most insects, in which ions are thought to enter basally either through a series of ion channels (Na+, K+ and Cl−) or through a bumetanide-sensitive Na+/K+/2Cl− cotransport. Apical fluxes are energised by a plasma-membrane H+-pumping V-ATPase, driving secretion of Na+ or K+ through one or more exchangers, at least one of which is amiloride-sensitive and appears to be closely similar to the Na+/H+ exchanger of vertebrates (Maddrell and O’Donnell, 1992). Cl− follows passively, perhaps through apical Cl− channels. Water follows the major ions, and haemolymph solutes diffuse across the tubule wall passively via a paracellular route. There are also transcellular active transport processes for certain metabolites or toxins, such as acylamides (Maddrell et al. 1974) and plant alkaloids (Maddrell, 1976; O’Donnell et al. 1983).
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