Horm Metab Res 1988; 20(10): 624-629
DOI: 10.1055/s-2007-1010901
ORIGINALS
Basic
© Georg Thieme Verlag, Stuttgart · New York

Endocrine Control of Cytosolic Factors Stimulating Adenylate Cyclase in Rat Lung

K. C. Chaudhary, M. S. Nijjar
  • Department of Pathology, Faculty of Medicine, University of Manitoba, Winnipeg, Canada
Department of Animal Sciences Punjab Agricultural University, Ludhiana, Punjab, India.Department of Pediatircs Alvin Buckwold Centre, University of Saskachewan, Saskatoon, Canada.
Further Information

Publication History

1987

1987

Publication Date:
14 March 2008 (online)

Summary

Endocrine control of cytoplasmic factors modulating adenylate cyclase activity in rat lung membranes was investigated. Hypophysectomy, adrenalectomy and thyroidectomy showed an adverse effect on the body and organ weights. Lung protein, glycogen and DNA contents were decreased in the endocrine ablated animals which were restored to the normal values on hormone treatment. Phosphodiesterase and phosphorylase activities were increased and decreased in adrenalectomized and thyroidectomized animals, respectively. The activities of these enzymes were restored to normal values on hormone treatment. Adrenalectomy and thyroidectomy affected ATPases differently.

Basal adenylate cyclase activity in rat lung membranes was not affected by adrenalectomy and hormone treatment. However, the total enzyme activity was increased by both dexamethasone (DEX) and thyroxine (T4) treatments. The activation of the particulate adenylate cyclase by the cytoplasmic factors was markedly decreased in the lung from hypophysectomized, adrenalectomized and thyroidectomized rats. This decrease in the cytoplasmic activation of adenylate cyclase was restored to or above the control values on hormone treatment. Alteration in the activation of the enzyme by cytoplasmic factors did not appear to be due to the change in the responsiveness of the enzyme. Glucocorticoids appeared to have a specific effect on the cytoplasmic factors modulating the enzyme.