1968
DOI: 10.1007/bf02147804
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2-Br-α-Ergokryptin: Beeinflussung von Fertilität und Laktation bei der Ratte

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Cited by 159 publications
(36 citation statements)
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“…It was developed originally to investigate whether metoclopramide would inr of prolactin secretion (12), crease adrenocortical sensitivity to angiotensin. Howrecognized to be a dopamine ever, we were not able to demonstrate any difference nocriptine has been demon-in the angiotensin-aldosterone dose-response curves pamine agonist in the central after metoclopramide.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…It was developed originally to investigate whether metoclopramide would inr of prolactin secretion (12), crease adrenocortical sensitivity to angiotensin. Howrecognized to be a dopamine ever, we were not able to demonstrate any difference nocriptine has been demon-in the angiotensin-aldosterone dose-response curves pamine agonist in the central after metoclopramide.…”
Section: Discussionmentioning
confidence: 99%
“…The subjects were placed on a constant diet containing 150 meq of sodium, 60 meq of potassium, 1 g of protein/kg and 2,860 cal/day for 5 d at the Clinical Research Center before the studies. Consecutive 24 h urine samples were collected for the first 4 d of the diet and consecutive 12 h urine samples were collected for the remainder of each study and were analyzed for sodium, potassium, and creatinine. No food was given after midnight before study day 1 when the subjects assumed the supine position until completion of each study.…”
Section: Methodsmentioning
confidence: 99%
“…This drug has not only been used to suppress prolactin secretion in laboratory animals (Fluckiger and Wagner, 1968), but also in mature cyclic ewes (Niswender, 1974) and in ram lambs (Ravault et al, 1977). As shown in figure 1, ergocryptine was quite effective in reducing serum prolactin during summer anestrus; yet average interval to first estrus was almost identical to that recorded for control ewes.…”
Section: Discussionmentioning
confidence: 99%
“…In 1978 Pawlikowski et al [3] showed that DA directly inhibits the pituitary growth The dopamine receptors, which are responsible for the direct effects of DA at the anterior pituitary level, were characterized as belonging to D2 type [for review see 4]. A synthesis of bromocriptine, a first selective and long-lasting agonist of D2 receptors, allowed to introduce this drug to the medical treatment of pituitary adenomas, particularly prolactinomas [5]. Nowadays bromocriptine and other newer D2 agonists consist a first line treatment for prolactinomas [6].…”
Section: Introductionmentioning
confidence: 99%