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21. |
Secretion of Vasopressin, Oxytocin, and Two Neurophysins from Rat Hypothalamo-Neurohypophyseal Explants in Organ Culture |
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Neuroendocrinology,
Volume 43,
Issue 2,
1986,
Page 252-258
Judy E. Stern,
Teresa Mitchell,
Victoria L. Herzberg,
William G. North,
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摘要:
Secretion of the neurohypophyseal principles arginine vasopressin, oxytocin, vasopressin-neurophysin, and oxytocin-neurophysin by hypothalamic-neurohypophyseal explants in organ culture was studied. The viability of explant cultures was tested on day 6 by their ability to incorporate 3H-amino acid into acid-precipitable protein, specifically vasopressin-neurophysin. The explants released all four neurosecretory products in a controlled manner during 8 successive days of culture. In addition, these substances were all present in neural lobes and hypothalami at the end of the culture period. Although the tissue retained a 1:1 molar ratio between the hormone and corresponding neurophysin, the levels of neurophysins in culture media were much higher than the levels of hormones. Through immunoprecipitation techniques we determined that both arginine vasopressin and oxytocin were unstable in culture media containing explants or in medium containing 10% heat-inactivated fetal calf serum. This suggests that neurophysins are more stable indicators of secretion by explants than are the corresponding hormones. An increased release of arginine vasopressin, oxytocin, vasopressin-neurophysin, and oxytocin-neurophysin occurred in response to elevated K+ and to increased sodium ions in the medium, and these four substances were released in different molecular proportions. The results indicate that explant cultures may be useful for comparisons of secretion of the two neurophysins and, to a more limited extent, of the two hormones in response to such stimuli.
ISSN:0028-3835
DOI:10.1159/000124534
出版商:S. Karger AG
年代:1986
数据来源: Karger
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22. |
Activation of Estradiol-Positive Feedback at Puberty: Estradiol Sensitizes the LHRH-Releasing System at Two Different Biochemical Steps |
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Neuroendocrinology,
Volume 43,
Issue 2,
1986,
Page 259-265
Sergio R. Ojeda,
Henryk F. Urbanski,
Kathy H. Katz,
Maria E. Costa,
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摘要:
Experiments were performed to examine whether estradiol (E2) can influence some of the intraneuronal mechanisms involved in luteinizing hormone-releasing hormone (LHRH) release during the onset of puberty in the female rat. The capacity of median eminence (ME) nerve terminals to secrete LHRH, as determined by both their basal release of LHRH and by their response to prostaglandin E2 (PGE2) in vitro, increased significantly during the juvenile-early peripubertal periods of development (postnatal days 22–34). Ovariectomy (OVX) on day 22 led to a striking reduction in LHRH response to PGE2 on day 34. E2 administered via s.c. Silastic capsules, at a dose that reproduces juvenile serum E2 levels, restored the response. Simulation of first proestrous serum E2 levels in late juvenile (28-day-old) female rats enhanced both the sensitivity and the responsivenes of LHRH-containing terminals to PGE2. Furthermore, E2 enhanced the sensitivity and the responsiveness of LHRH terminals to norepinephrine (NE). This effect appeared to be related to both the increased LHRH response to PGE2 and an enhanced sensitivity of the PGE2-synthesizing pathway to NE. This is because MEs from E2-treated rats showed a marked increase in PGE2 release in response to a NE concentration which was barely effective in untreated controls. It is suggested that one of the mechanisms by which E2 activates the first preovulatory discharge of LHRH release in the female rat is by facilitating the occurrence of two different but sequentially related biochemical events: the stimulation of PGE2 formation by NE and the enhancement of LHRH release by PGE2. In addition, it appears that maintenance of LHRH responsiveness to PGE2, which has been implicated as an obligatory component of NE-induced LHRH release, is E=-dependen
ISSN:0028-3835
DOI:10.1159/000124535
出版商:S. Karger AG
年代:1986
数据来源: Karger
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23. |
Down-Regulation of Growth Hormone Releasing Factor Receptors following Continuous Infusion of Growth Hormone Releasing Factor in vivo |
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Neuroendocrinology,
Volume 43,
Issue 2,
1986,
Page 266-268
William B. Wehrenberg,
Hans Seifert,
Louise M. Bilezikjian,
Wylie Vale,
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摘要:
The in vivo chronic infusion of growth hormone releasing factor (GRF) results in a loss of the pituitary growth hormone (GH) response to GRF as well as in a substantial depletion of pituitary GH content. To evaluate if the loss in response is due to the down-regulation of GRF receptors the specific GRF binding capacity of pituitary homogenates prepared from rats infused with saline or GRF (1 or 15 µg/h for 24 h) was determined. The pituitary binding capacity of animals infused with GRF was significantly reduced as compared to animals infused with saline
ISSN:0028-3835
DOI:10.1159/000124538
出版商:S. Karger AG
年代:1986
数据来源: Karger
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