Arginine vasopressin stimulates phosphoinositide turnover in an enriched rat Leydig cell preparation

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Arginine vasopressin stimulates phosphoinositide turnover in an enriched rat Leydig cell preparation. / Nielsen, J.R.; Hansen, Harald S.; Jensen, B.

In: Molecular and Cellular Endocrinology, Vol. 61, No. 2, 01.01.1989, p. 181-188.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Nielsen, JR, Hansen, HS & Jensen, B 1989, 'Arginine vasopressin stimulates phosphoinositide turnover in an enriched rat Leydig cell preparation', Molecular and Cellular Endocrinology, vol. 61, no. 2, pp. 181-188.

APA

Nielsen, J. R., Hansen, H. S., & Jensen, B. (1989). Arginine vasopressin stimulates phosphoinositide turnover in an enriched rat Leydig cell preparation. Molecular and Cellular Endocrinology, 61(2), 181-188.

Vancouver

Nielsen JR, Hansen HS, Jensen B. Arginine vasopressin stimulates phosphoinositide turnover in an enriched rat Leydig cell preparation. Molecular and Cellular Endocrinology. 1989 Jan 1;61(2):181-188.

Author

Nielsen, J.R. ; Hansen, Harald S. ; Jensen, B. / Arginine vasopressin stimulates phosphoinositide turnover in an enriched rat Leydig cell preparation. In: Molecular and Cellular Endocrinology. 1989 ; Vol. 61, No. 2. pp. 181-188.

Bibtex

@article{447b7c4c2f974f28a2c5b4d5382fcb17,
title = "Arginine vasopressin stimulates phosphoinositide turnover in an enriched rat Leydig cell preparation",
abstract = "An enriched rat Leydig cell preparation was preincubated with [C]arachidonic acid. Stimulation of the cells with arginine vasopressin (AVP) (1 µM) for 2 min caused a significant increase in labelled phosphatidic acid and a significant fall in radioactivity in phosphatidylinositol and phosphatidylinositol 4-monophosphate + phosphatidylinositol 4,5-bisphosphate. Preincubation with dibutyryl cyclic AMP had no effect on the AVP-induced phospholipid turnover. Leydig cells were preincubated with myo-[2-H]inositol for 22 h and then with 10 mM LiCl for 10 min. Exposure to AVP (1 µM) induced a rise in labelled inositol phosphates. The response was inhibited when the cells were preincubated with the phorbol ester, 4{\ss}-phorbol 12-myristate 13-acetate (0.16 µM) for 10 min. These results provide evidence for an AVP-induced phospholipase C stimulation in rat Leydig cells and suggest a protein kinase C-dependent feedback inhibition of the stimulation. Other agonists that might have a regulatory function in the testis were tested for possible effects on phosphoinositide metabolism. Of prostaglandin E (10 µm), angiotensin II (0.1 µM), and bradykinin (0.9 µM), only the latter induced a significant increase in the labelled inositol phosphates. This suggests that Leydig cells possess a bradykinin receptor which can activate phospholipase C.",
author = "J.R. Nielsen and Hansen, {Harald S.} and B. Jensen",
year = "1989",
month = jan,
day = "1",
language = "English",
volume = "61",
pages = "181--188",
journal = "Molecular and Cellular Endocrinology",
issn = "0303-7207",
publisher = "Elsevier Ireland Ltd",
number = "2",

}

RIS

TY - JOUR

T1 - Arginine vasopressin stimulates phosphoinositide turnover in an enriched rat Leydig cell preparation

AU - Nielsen, J.R.

AU - Hansen, Harald S.

AU - Jensen, B.

PY - 1989/1/1

Y1 - 1989/1/1

N2 - An enriched rat Leydig cell preparation was preincubated with [C]arachidonic acid. Stimulation of the cells with arginine vasopressin (AVP) (1 µM) for 2 min caused a significant increase in labelled phosphatidic acid and a significant fall in radioactivity in phosphatidylinositol and phosphatidylinositol 4-monophosphate + phosphatidylinositol 4,5-bisphosphate. Preincubation with dibutyryl cyclic AMP had no effect on the AVP-induced phospholipid turnover. Leydig cells were preincubated with myo-[2-H]inositol for 22 h and then with 10 mM LiCl for 10 min. Exposure to AVP (1 µM) induced a rise in labelled inositol phosphates. The response was inhibited when the cells were preincubated with the phorbol ester, 4ß-phorbol 12-myristate 13-acetate (0.16 µM) for 10 min. These results provide evidence for an AVP-induced phospholipase C stimulation in rat Leydig cells and suggest a protein kinase C-dependent feedback inhibition of the stimulation. Other agonists that might have a regulatory function in the testis were tested for possible effects on phosphoinositide metabolism. Of prostaglandin E (10 µm), angiotensin II (0.1 µM), and bradykinin (0.9 µM), only the latter induced a significant increase in the labelled inositol phosphates. This suggests that Leydig cells possess a bradykinin receptor which can activate phospholipase C.

AB - An enriched rat Leydig cell preparation was preincubated with [C]arachidonic acid. Stimulation of the cells with arginine vasopressin (AVP) (1 µM) for 2 min caused a significant increase in labelled phosphatidic acid and a significant fall in radioactivity in phosphatidylinositol and phosphatidylinositol 4-monophosphate + phosphatidylinositol 4,5-bisphosphate. Preincubation with dibutyryl cyclic AMP had no effect on the AVP-induced phospholipid turnover. Leydig cells were preincubated with myo-[2-H]inositol for 22 h and then with 10 mM LiCl for 10 min. Exposure to AVP (1 µM) induced a rise in labelled inositol phosphates. The response was inhibited when the cells were preincubated with the phorbol ester, 4ß-phorbol 12-myristate 13-acetate (0.16 µM) for 10 min. These results provide evidence for an AVP-induced phospholipase C stimulation in rat Leydig cells and suggest a protein kinase C-dependent feedback inhibition of the stimulation. Other agonists that might have a regulatory function in the testis were tested for possible effects on phosphoinositide metabolism. Of prostaglandin E (10 µm), angiotensin II (0.1 µM), and bradykinin (0.9 µM), only the latter induced a significant increase in the labelled inositol phosphates. This suggests that Leydig cells possess a bradykinin receptor which can activate phospholipase C.

UR - http://www.scopus.com/inward/record.url?scp=0024501126&partnerID=8YFLogxK

M3 - Journal article

AN - SCOPUS:0024501126

VL - 61

SP - 181

EP - 188

JO - Molecular and Cellular Endocrinology

JF - Molecular and Cellular Endocrinology

SN - 0303-7207

IS - 2

ER -

ID: 45561822