Effects of LHRH and ANG II on prolactin stimulation are mediated by hypophysial AT1 receptor subtype

We have used the nonpeptide angiotensin II (ANG II) receptor antagonists losartan (receptor subtype AT1) and PD-123319 (AT2) to determine the participation of ANG II receptor subtypes in luteinizing hormone-releasing hormone (LHRH)-induced prolactin release in a perifusion study using intact pituita...

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Detalles Bibliográficos
Autor principal: Becu-Villalobos, D.
Otros Autores: Lacau-Mengido, I.M, Thyssen, S.M, Diaz-Torga, G.S, Libertun, C.
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 1994
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Acceso en línea:Registro en Scopus
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Registro en la Biblioteca Digital
Aporte de:Registro referencial: Solicitar el recurso aquí
LEADER 05020caa a22008897a 4500
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008 190411s1994 xx ||||fo|||| 00| 0 eng|d
024 7 |2 scopus  |a 2-s2.0-0028260124 
024 7 |2 cas  |a 1 (4 dimethylamino 3 methylbenzyl) 5 diphenylacetyl 4,5,6,7 tetrahydro 1h imidazo[4,5 c]pyridine 6 carboxylic acid, 130663-39-7; angiotensin, 11128-99-7, 1407-47-2; follitropin, 9002-68-0; gonadorelin, 33515-09-2, 9034-40-6; losartan potassium, 124750-99-8; losartan, 114798-26-4; luteinizing hormone, 39341-83-8, 9002-67-9; prolactin, 12585-34-1, 50647-00-2, 9002-62-4; Angiotensin II, 11128-99-7; Biphenyl Compounds; Gonadorelin, 33515-09-2; Imidazoles; Losartan, 114798-26-4; PD 123319, 130663-39-7; Prolactin, 9002-62-4; Pyridines; Receptors, Angiotensin; Tetrazoles 
040 |a Scopus  |b spa  |c AR-BaUEN  |d AR-BaUEN 
030 |a AJPMD 
100 1 |a Becu-Villalobos, D. 
245 1 0 |a Effects of LHRH and ANG II on prolactin stimulation are mediated by hypophysial AT1 receptor subtype 
260 |c 1994 
270 1 0 |m Libertun, C.; Laboratorio de Neuroendocrinologia, IBME, CONICET, V. Obligado 2490, 1428 Buenos Aires, Argentina 
506 |2 openaire  |e Política editorial 
520 3 |a We have used the nonpeptide angiotensin II (ANG II) receptor antagonists losartan (receptor subtype AT1) and PD-123319 (AT2) to determine the participation of ANG II receptor subtypes in luteinizing hormone-releasing hormone (LHRH)-induced prolactin release in a perifusion study using intact pituitaries in vitro. LHRH (1.85 x 10-7 M) released prolactin consistently, whereas losartan (10-5 M) abolished prolactin response without modifying basal prolactin or luteinizing hormone (LH) and follicle-stimulating hormone (FSH) release. PD-123319 (10-5 M) had no effect on basal or LHRH-induced prolactin, LH, or FSH release. We also determined that the effect of ANG II on prolactin release was mediated by the same receptor subtype. In adenohypophysial cells dispersed in vitro ANG II (10-8 M) released prolactin. Losartan (10-7 and 10-6 M), but not PD-123319, inhibited this effect. We conclude that in intact hypophyses of 15-day-old female rats the effect of LHRH on prolactin release is readily demonstrated. LHRH-induced prolactin release appears to be mediated by ANG II acting in a paracrine manner on AT1 receptors located on lactotrophs.  |l eng 
593 |a Laboratorio de Neuroendocrinologia, IBME, CONICET, V. Obligado 2490, 1428 Buenos Aires, Argentina 
690 1 0 |a ANGIOTENSIN II RECEPTOR SUBTYPES 
690 1 0 |a LOSARTAN 
690 1 0 |a LUTEINIZING HORMONE-RELEASING HORMONE 
690 1 0 |a PARACRINE 
690 1 0 |a PD-123319 
690 1 0 |a PITUITARY 
690 1 0 |a 1 (4 DIMETHYLAMINO 3 METHYLBENZYL) 5 DIPHENYLACETYL 4,5,6,7 TETRAHYDRO 1H IMIDAZO[4,5 C]PYRIDINE 6 CARBOXYLIC ACID 
690 1 0 |a ANGIOTENSIN 
690 1 0 |a ANGIOTENSIN RECEPTOR 
690 1 0 |a FOLLITROPIN 
690 1 0 |a GONADORELIN 
690 1 0 |a LOSARTAN 
690 1 0 |a LOSARTAN POTASSIUM 
690 1 0 |a LUTEINIZING HORMONE 
690 1 0 |a PROLACTIN 
690 1 0 |a RECEPTOR SUBTYPE 
690 1 0 |a ADENOHYPOPHYSIS 
690 1 0 |a ANIMAL CELL 
690 1 0 |a ANIMAL TISSUE 
690 1 0 |a ARTICLE 
690 1 0 |a CONTROLLED STUDY 
690 1 0 |a FEMALE 
690 1 0 |a FOLLITROPIN RELEASE 
690 1 0 |a LUTEINIZING HORMONE RELEASE 
690 1 0 |a NONHUMAN 
690 1 0 |a PRIORITY JOURNAL 
690 1 0 |a PROLACTIN RELEASE 
690 1 0 |a PROLACTIN SECRETING CELL 
690 1 0 |a RAT 
690 1 0 |a ANGIOTENSIN II 
690 1 0 |a ANIMAL 
690 1 0 |a BIPHENYL COMPOUNDS 
690 1 0 |a FEMALE 
690 1 0 |a GONADORELIN 
690 1 0 |a IMIDAZOLES 
690 1 0 |a IN VITRO 
690 1 0 |a LOSARTAN 
690 1 0 |a PERFUSION 
690 1 0 |a PITUITARY GLAND 
690 1 0 |a PROLACTIN 
690 1 0 |a PYRIDINES 
690 1 0 |a RATS 
690 1 0 |a RATS, SPRAGUE-DAWLEY 
690 1 0 |a RECEPTORS, ANGIOTENSIN 
690 1 0 |a SUPPORT, NON-U.S. GOV'T 
690 1 0 |a TETRAZOLES 
653 0 0 |a dup 753, du pont merck, United States; pd 123319, parke davis, United States 
700 1 |a Lacau-Mengido, I.M. 
700 1 |a Thyssen, S.M. 
700 1 |a Diaz-Torga, G.S. 
700 1 |a Libertun, C. 
773 0 |d 1994  |g v. 266  |h pp. E274-E278  |k n. 2 29-2  |p AM. J. PHYSIOL. ENDOCRINOL. METAB.  |x 00029513  |w (AR-BaUEN)CENRE-1678  |t American Journal of Physiology - Endocrinology and Metabolism 
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856 4 0 |u https://hdl.handle.net/20.500.12110/paper_00029513_v266_n229-2_pE274_BecuVillalobos  |y Handle 
856 4 0 |u https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00029513_v266_n229-2_pE274_BecuVillalobos  |y Registro en la Biblioteca Digital 
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