IN VITRO STUDIES OF THE RELEASE MECHANISM FOR VASOPRESSIN IN RATS
- 1 December 1966
- journal article
- research article
- Published by Oxford University Press (OUP) in Acta Endocrinologica
- Vol. 53 (4) , 644-654
- https://doi.org/10.1530/acta.0.0530644
Abstract
A study was made of the release of vasopressin activity from groups of isolated posterior pituitary hemilobes of rats, incubated in media with different ionic compositions and with different drugs added to the medium. Nicotine, amyl nitrite and ATP, which have been reported to cause a large in vivo release of hormone had no significant releasing effect in vitro. Caffeine too did not cause any release of hormone activity. About 5% of the vasopressin activity extractable from the isolated posterior pituitary hemilobes was released during stimulation with a high concentration of potassium in the medium. No more than this percentage could be mobilized during such a stimulation, even after further subdivision of the posterior pituitary glands, prolongation of the stimulation period or after increasing the calcium concentration in the medium five-fold. No release into the medium of vasopressin binding protein could be demonstrated during stimulation of vasopressin release. The results seem to be in agreement with the hypothesis that the release of vasopressin is intimately associated with arrival of impulses to the nerve endings in the posterior pituitary gland and that it takes place from a small pool of readily available hormone, presumably by dissociation of the hormone from the carrier protein.This publication has 3 references indexed in Scilit:
- ROLE OF CALCIUM IN THE RELEASE OF VASOPRESSIN AND OXYTOCIN FROM POSTERIOR PITUITARY PROTEINActa Endocrinologica, 1965
- BINDING OF VASOPRESSIN AND OXYTOCIN TO PROTEIN IN EXTRACTS OF BOVINE AND RABBIT NEUROHYPOPHYSESJournal of Endocrinology, 1964
- L'ocytocine et la vasopressine du mouton: Reconstitution d'un complexe hormonal actifBiochimica et Biophysica Acta, 1959