By J.E. Treherne
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Additional resources for Advances in Insect Physiology, Vol. 9
18, 327-333. Bentley, P. J. (1960). The effects of vasopressin on the short-circuit current across the wall of the isolated toad bladder, Bufo marinus. J. Endocr. 21, 161-170. Bentley, P. J . (1 967). Natriferic and hydro-osmotic effects on the toad bladder of vasopressin analogues with selective antidiuretic activity. J. Endocr. 39, 299-304. Berridge, M. J. (1 970). The role of 5-hydroxytryptamine and cyclic AMP in the control of fluid secretion by isolated salivary glands. J. exp. Biol. 5 3 , 171-186.
T. , Bdolah, A. and Schramm, M. (1967). The mechanism of enzyme secretion by the cell. 4. Effects of inducers, substrates and inhibitors on amylase secretion by rat parotid slices. Eur. J. Biochem. 1, 96-101. Bdolah, A. and Schramm, M. (1965). The function of 3‘,5‘ cyclic AMP in enzyme secretion. Biochem. biophys. Res. Commun. 18,452-454. Bentley, P. J . (1 959). The effects of ionic changes on water transfer across the isolated urinary bladder of the toad, Bufo marinus. J. Endocr. 18, 327-333.
The subsequent activation of cation and anion pumps then induces a biphasic potential response associated with the beginning of fluid secretion. , 1971). Apart from these studies on the diuretic hormones of Rhodnius there is very little information on the mode of action of this second group of hormones in insects. The present study on the control of fluid secretion by salivary glands may provide a basic model for hormones concerned with regulating the short-term activity of insect cells. Due to our lack of knowledge about the mode of action of insect hormones, the general significance of this model for the control of secretion by salivary glands must be assessed by comparing the mode of action of 5-HT (summarized in Fig.