All Relations between somatostatin and insulin

Publication Sentence Publish Date Extraction Date Species
J Tamarit-Rodriguez, E Vara, J Tamari. Starvation-induced secretory changes of insulin, somatostatin, and glucagon and their modification by 2-bromostearate. Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme. vol 16. issue 3. 1984-06-20. PMID:6143716. starvation for 48 h blocked both the glucose-induced stimulation and inhibition of insulin and somatostatin and the glucagon secretion. 1984-06-20 2023-08-12 Not clear
J Tamarit-Rodriguez, E Vara, J Tamari. Starvation-induced secretory changes of insulin, somatostatin, and glucagon and their modification by 2-bromostearate. Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme. vol 16. issue 3. 1984-06-20. PMID:6143716. brs completely restored the insulin response and stimulated both somatostatin and glucagon-basal release, the latter inhibition by glucose being partially recovered. 1984-06-20 2023-08-12 Not clear
J Tamarit-Rodriguez, E Vara, J Tamari. Starvation-induced secretory changes of insulin, somatostatin, and glucagon and their modification by 2-bromostearate. Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme. vol 16. issue 3. 1984-06-20. PMID:6143716. palmitate transient stimulation of insulin and somatostatin and inhibition of glucagon release was turned into a sustained increase in all three cases by addition of brs. 1984-06-20 2023-08-12 Not clear
J Kasurinen, K J Syrjäne. Stainability of the peptide hormones in gastrointestinal apudomas as demonstrated by immunoperoxidase kits. Scandinavian journal of gastroenterology. vol 19. issue 2. 1984-06-20. PMID:6144178. a series of 25 apudomas of the gastrointestinal tract (22 cases), bronchus (2 cases), and thymus (1 case) were subjected to staining with silver impregnation (masson-fontana and grimelius) techniques and with the commercial immunoperoxidase kits for the peptide hormones adrenocorticotropin, calcitonin, gastrin, glucagon, growth hormone, human chorionic gonadotropin (hcg), insulin, somatostatin, and vasoactive intestinal peptide. 1984-06-20 2023-08-12 human
U Keller, H Schnell, J Girard, W Stauffache. Effect of physiological elevation of plasma growth hormone levels on ketone body kinetics and lipolysis in normal and acutely insulin-deficient man. Diabetologia. vol 26. issue 2. 1984-06-18. PMID:6143702. during somatostatin-induced acute insulin deficiency (n = 7), growth hormone enhanced the increase in total ketone body production observed in six subjects receiving somatostatin alone (8.4 +/- 0.8 versus 4.1 +/- 0.7 mumol x kg-1 x min-1, p less than 0.01). 1984-06-18 2023-08-12 human
A M Bucha. An immunocytochemical study of endocrine pancreas of snakes. Cell and tissue research. vol 235. issue 3. 1984-06-18. PMID:6370448. of the eleven peptides studied, insulin, pancreatic glucagon and somatostatin were present in endocrine cells within the islets of all the species investigated. 1984-06-18 2023-08-12 Not clear
A Pernet, V A Hammond, G Blesa-Malpica, J Burrin, H Orskov, K G Alberti, D G Johnsto. The metabolic effects of dopamine in man. European journal of clinical pharmacology. vol 26. issue 1. 1984-06-06. PMID:6143668. somatostatin alone induced a progressive rise in circulating non-esterified fatty acid and 3-hydroxybutyrate levels reflecting insulin deficiency. 1984-06-06 2023-08-12 Not clear
Y Seino, S Seino, M Usami, K Tsuda, J Takemura, S Nishi, H Ishida, H Imur. Somatostatin, glucagon, and insulin secretion from isolated perfused pancreas of new genetically obese hyperglycemic rats. Metabolism: clinical and experimental. vol 33. issue 5. 1984-06-05. PMID:6144033. somatostatin, glucagon, and insulin secretion from isolated perfused pancreas of new genetically obese hyperglycemic rats. 1984-06-05 2023-08-12 rat
Y Seino, S Seino, M Usami, K Tsuda, J Takemura, S Nishi, H Ishida, H Imur. Somatostatin, glucagon, and insulin secretion from isolated perfused pancreas of new genetically obese hyperglycemic rats. Metabolism: clinical and experimental. vol 33. issue 5. 1984-06-05. PMID:6144033. insulin, somatostatin, and glucagon release from the perfused pancreas was studied in the newly developed genetically obese hyperglycemic hyperinsulinemic (wistar fatty) rat. 1984-06-05 2023-08-12 rat
Y Seino, S Seino, M Usami, K Tsuda, J Takemura, S Nishi, H Ishida, H Imur. Somatostatin, glucagon, and insulin secretion from isolated perfused pancreas of new genetically obese hyperglycemic rats. Metabolism: clinical and experimental. vol 33. issue 5. 1984-06-05. PMID:6144033. insulin and somatostatin levels rose significantly compared to those in lean littermate controls during arginine infusion. 1984-06-05 2023-08-12 rat
Y Seino, S Seino, M Usami, K Tsuda, J Takemura, S Nishi, H Ishida, H Imur. Somatostatin, glucagon, and insulin secretion from isolated perfused pancreas of new genetically obese hyperglycemic rats. Metabolism: clinical and experimental. vol 33. issue 5. 1984-06-05. PMID:6144033. these results show that hypersecretion of insulin and somatostatin in vitro may suppress glucagon release in wistar fatty rats. 1984-06-05 2023-08-12 rat
G C Weir, P A Halban, P Meda, C B Wollheim, L Orci, A E Renol. Dispersed adult rat pancreatic islet cells in culture: A, B, and D cell function. Metabolism: clinical and experimental. vol 33. issue 5. 1984-06-05. PMID:6201694. since freshly dispersed adult rat islet cells failed to respond appropriately to secretagogues (no alteration in insulin, glucagon, or somatostatin release after glucose change; modest response to ibmx), these cells were established in primary monolayer culture. 1984-06-05 2023-08-12 rat
G C Weir, P A Halban, P Meda, C B Wollheim, L Orci, A E Renol. Dispersed adult rat pancreatic islet cells in culture: A, B, and D cell function. Metabolism: clinical and experimental. vol 33. issue 5. 1984-06-05. PMID:6201694. whereas the ratio of somatostatin:insulin content was similar for islets and cells (approximately 0.7:100), the dispersed cell population appeared depleted in glucagon (glucagon:insulin ratios being 17:100 for islets and 4:100 for cells) reflecting either degranulation or relative loss of a cells. 1984-06-05 2023-08-12 rat
K Hermanse. Effects of cholecystokinin (CCK)-4, nonsulfated CCK-8, and sulfated CCK-8 on pancreatic somatostatin, insulin, and glucagon secretion in the dog: studies in vitro. Endocrinology. vol 114. issue 5. 1984-05-30. PMID:6143659. effects of cholecystokinin (cck)-4, nonsulfated cck-8, and sulfated cck-8 on pancreatic somatostatin, insulin, and glucagon secretion in the dog: studies in vitro. 1984-05-30 2023-08-12 dog
Y Tanaka, Y Seino, M Ishida, K Yamaoka, H Yabuuchi, H Ishida, S Seino, Y Seino, H Imur. Effect of vitamin D3 on the pancreatic secretion of insulin and somatostatin. Acta endocrinologica. vol 105. issue 4. 1984-05-30. PMID:6144227. effect of vitamin d3 on the pancreatic secretion of insulin and somatostatin. 1984-05-30 2023-08-12 rat
Y Tanaka, Y Seino, M Ishida, K Yamaoka, H Yabuuchi, H Ishida, S Seino, Y Seino, H Imur. Effect of vitamin D3 on the pancreatic secretion of insulin and somatostatin. Acta endocrinologica. vol 105. issue 4. 1984-05-30. PMID:6144227. to clarify the role of vitamin d in the regulation of the endocrine pancreas, we have studied insulin and somatostatin secretion in vitamin d deficient rats (reared on a vitamin d deficient diet), d-replete rats (reared on a vitamin d deficient diet and given 160 iu of vitamin d3 sc twice a week) and control rats (reared on laboratory chow), using the isolated perfused rat pancreas. 1984-05-30 2023-08-12 rat
P P Gerber, E R Trimble, L Herberg, A E Renol. Glucose-induced somatostatin secretion by the rat pancreas is not potentiated by glucose. Acta endocrinologica. vol 105. issue 4. 1984-05-30. PMID:6144228. the effect of previous exposure to glucose on subsequent glucose-stimulated insulin and somatostatin secretion has been investigated using the isolated perfused rat pancreas. 1984-05-30 2023-08-12 rat
P P Gerber, E R Trimble, L Herberg, A E Renol. Glucose-induced somatostatin secretion by the rat pancreas is not potentiated by glucose. Acta endocrinologica. vol 105. issue 4. 1984-05-30. PMID:6144228. since exogenous insulin is known to inhibit glucose-induced somatostatin secretion, it seemed possible that lack of visible potentiation of glucose-induced somatostatin secretion by glucose could have been due to partial d cell inhibition by simultaneously augmented insulin secretion during the second glucose stimulation. 1984-05-30 2023-08-12 rat
P P Gerber, E R Trimble, L Herberg, A E Renol. Glucose-induced somatostatin secretion by the rat pancreas is not potentiated by glucose. Acta endocrinologica. vol 105. issue 4. 1984-05-30. PMID:6144228. in an attempt to exclude such an interaction between b and d cells, somatostatin secretion was also studied in the pancreases of spontaneously diabetic, wistar (bb) rats (these animals are insulin deficient and are maintained by daily injections of insulin). 1984-05-30 2023-08-12 rat
P P Gerber, E R Trimble, L Herberg, A E Renol. Glucose-induced somatostatin secretion by the rat pancreas is not potentiated by glucose. Acta endocrinologica. vol 105. issue 4. 1984-05-30. PMID:6144228. however, even though insulin secretion was not detectable from these pancreases, glucose potentiation of glucose-induced somatostatin secretion did not occur. 1984-05-30 2023-08-12 rat