Central control of peripheral circulating somatostatin in dogs: effect of 2-deoxyglucose

E. Ipp, U. Piran, H. Richter, C. Garberoglio, A. Moossa and A. H. Rubenstein Circulating plasma somatostatin concentrations are known to fluctuate in response to nutrients and hormones. However, little is known about neural or central nervous system (CNS) control of somatostatin secretion. To test w...

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Veröffentlicht in:American journal of physiology: endocrinology and metabolism 1982-09, Vol.243 (3), p.E213-E216
Hauptverfasser: Ipp, E, Piran, U, Richter, H, Garberoglio, C, Moossa, A, Rubenstein, A. H
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Sprache:eng
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Zusammenfassung:E. Ipp, U. Piran, H. Richter, C. Garberoglio, A. Moossa and A. H. Rubenstein Circulating plasma somatostatin concentrations are known to fluctuate in response to nutrients and hormones. However, little is known about neural or central nervous system (CNS) control of somatostatin secretion. To test whether peripheral circulating somatostatin is influenced by a central stimulus, 2-deoxyglucose (37.5 mg/kg) was infused into a lateral cerebral ventricle of six conscious dogs over a period of 15 min. Plasma somatostatin levels rose from a base line of 105 +/- 6 pg/ml (mean +/- SE) to a peak of 154 +/- 10 pg/ml (P less than 0.005) at 30 min after the onset of the infusion. Somatostatin levels were still significantly elevated (P less than 0.025) at 60 min (119 +/- 6 pg/ml) and thereafter gradually returned toward base line. Plasma glucose and glucagon levels increased in response to intraventricular 2-deoxyglucose. Glucose concentrations rose from 105 +/- 5 mg/dl to peak at 203 +/- 16 mg/dl (P less than 0.005) at 80 min and remained elevated to 120 min. The concentration of plasma glucagon increased from 41 +/- 6 to 92 +/- 18 pg/ml at 60 min (P less than 0.05) and then declined. In marked contrast to intraventricular 2-deoxyglucose, similar concentrations of 2-deoxyglucose administered intravenously (n = 4) resulted in a slight fall in plasma somatostatin. Intraventricular saline did not result in a change in plasma somatostatin. It is concluded that peripheral circulating somatostatin may be susceptible to central nervous system control.
ISSN:0193-1849
0002-9513
1522-1555
DOI:10.1152/ajpendo.1982.243.3.e213