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11. |
Hypophyseal Actions of Pulsatile Gonadotropin-Releasing Hormone in the Ewe: Development and Application of a New Experimental Model |
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Neuroendocrinology,
Volume 48,
Issue 3,
1988,
Page 287-295
Alan H. Kaynard,
Fred J. Karsch,
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摘要:
Ovariectomy of ewes during seasonal anestrus and immediate replacement with subcutaneous Silastic progesterone implants which maintained a midluteal-phase level of circulating progesterone obliterated pulsatile luteinizing hormone (LH) secretion for up to 2 weeks without preventing a normal response of the pituitary to exogenous pulses of gonadotropin-releasing hormone (GnRH). Consideration was given to the possibility that such ‘progesterone-suppressed ewes’ would be useful as an animal model for isolating the pituitary from pulsatile GnRH secretion, and for testing the hypophyseotropic actions of exogenous GnRH. Two experiments were conducted using this progesterone-suppressed ewe as an animal model. In the first, the amplitude of LH pulses elicited by episodic delivery of GnRH was found to depend upon the frequency of exogenous GnRH pulses. Hourly frequency produced larger LH pulses than a 30-min frequency of GnRH. In the second experiment, LH surges were induced in progesterone-suppressed ewes by a combined treatment of estradiol and GnRH in patterns designed to approximate those secreted in the follicular phase of the estrous cycle. Our findings suggest that the progesterone-suppressed ewe is a suitable animal model for studying the hypophyseotropic actions of GnRH. Further, they are consistent with two hypotheses concerning the regulation of the tonic and surge modes of LH secretion. (1) The inverse relationship between LH pulse frequency and amplitude observed in a number of situations can be accounted for, at least in part, by a differential response of the pituitary to GnRH. (2) Progesterone can block the LH surge by an action on the brain and an inhibition of pulsatile GnRH rele
ISSN:0028-3835
DOI:10.1159/000125024
出版商:S. Karger AG
年代:1988
数据来源: Karger
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12. |
Importance of Pituitary and Neural Actions of Estradiol in Induction of the Luteinizing Hormone Surge in the Ewe |
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Neuroendocrinology,
Volume 48,
Issue 3,
1988,
Page 296-303
Alan H. Kaynard,
Benoît Malpaux,
Jane E. Robinson,
Nancy L. Wayne,
Fred J. Karsch,
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摘要:
Two experiments were performed to test the importance of both pituitary and neural sites of action of estradiol in inducing the surge of luteinizing hormone (LH) in the ewe. Both experiments were conducted using an animal model in which pulsatile secretion of gonadotropin-releasing hormone (GnRH) and endogenous secretion of ovarian steroids were eliminated by ovariectomy during seasonal anestrus and treatment with Silastic implants which maintained a luteal-phase level of serum progesterone. The hormonal requirements for the surge were then evaluated by systematic application of GnRH and estradiol signals using pulsatile infusion pumps (for GnRH) and Silastic implants (for estradiol). In experiment 1 the circulating level of estradiol and frequency of GnRH pulses were increased either abruptly or progressively (i.e. mimicking the changes in the estrous cycle between luteolysis and just before the LH surge). Abrupt increments led to an LH surge in all ewes; progressive rises to the same absolute levels did not. However, sudden application of a further large increase in GnRH upon the progressive rise elicited an LH surge in every instance. In experiment 2, a GnRH pulse pattern known to be effective in inducing the LH surge was applied under conditions of differing estradiol concentration: no estradiol, basal estradiol, basal rising to peak estradiol. The GnRH signal elicited high-amplitude surges of LH only in the presence of a peak estradiol concentration. Our findings are consistent with the conclusion that two actions are required for a rise in estradiol to elicit a full-amplitude surge of LH in the ewe: an action on the brain to evoke a sudden increase in GnRH release and an action on the pituitary to maximize its response to GnRH.
ISSN:0028-3835
DOI:10.1159/000125025
出版商:S. Karger AG
年代:1988
数据来源: Karger
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13. |
Lack of Acuted-Amphetamine Effects on Thyrotropin Release |
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Neuroendocrinology,
Volume 48,
Issue 3,
1988,
Page 304-307
Karley Y. Little,
James C. Garbutt,
James P. Mayo,
George Mason,
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摘要:
Case reports have suggested that amphetamine abuse causes excessive secretion of thyrotropin (TSH) and thyroxine (T4). Such an amphetamine-induced effect might be noradrenergic-mediated in the hypothalamus. The current controlled study examined oral d-amphetamine effects on the hypothalamic-pituitary-thyroid axis in normal humans. No acute effects were seen on TSH, T3 or T4 levels, d-Amphetamine elevated cortisol levels at 180 min, as previously reported.
ISSN:0028-3835
DOI:10.1159/000125026
出版商:S. Karger AG
年代:1988
数据来源: Karger
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14. |
Twenty-Four-Hour Patterns of Pineal Melatonin and Pituitary and Plasma Prolactin in Male Rats under ‘Natural’ and Artificial Lighting Conditions |
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Neuroendocrinology,
Volume 48,
Issue 3,
1988,
Page 308-313
Maija-Liisa Laakso,
Tarja Porkka-Heiskanen,
Aino Alila,
Mikael Peder,
Gunnar Johansson,
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摘要:
Natural lighting differs from usual artificial lighting mainly as follows: it has larger spectral composition, fluctuations of intensity during the day, higher intensity levels during the night (moonlight, starlight), and gradual changes of illuminance at dawn and dusk. The present experiment was performed in order to study whether these features of lighting affect the 24-hour patterns of melatonin and prolactin in male rats. The rats were kept 7 days in ‘natural’ lighting (sunlight through windows) or in artificial lighting (cool white fluorescent lamps) of similar periodicities (13/1 lh light/ dark). The samples were collected at 3-hour intervals during a 24-hour period. Pineal melatonin contents, pituitary prolactin contents, and plasma prolactin concentrations were measured radioimmunologically. The nocturnal pineal melatonin contents were higher and the daytime contents lower in natural than in artificial lighting conditions. A corresponding ‘strengthening of rhythm’ of prolactin was found in natural lighting. A reason for the higher amplitude variation of melatonin in the natural lighting conditions may be the gradual changes of illuminance at dawn and dusk. The different pituitary and plasma prolactin patterns of the rats kept in the two lighting conditions might partly be explained by a stimulatory effect of melatonin on the production and secretion of prolactin, but other regulatory factors had to be involv
ISSN:0028-3835
DOI:10.1159/000125027
出版商:S. Karger AG
年代:1988
数据来源: Karger
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15. |
Differential Effects of Pituitary Stalk-Section on Posterior Pituitary and Hypothalamic Contents of Prolactin-Releasing Factor, Oxytocin, Dopamine and Beta-Endorphin |
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Neuroendocrinology,
Volume 48,
Issue 3,
1988,
Page 314-319
James F. Hyde,
Ichiro Murai,
Nira Ben-Jonathan,
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摘要:
We have recently shown that the posterior pituitary (neurointermediate lobe) contains a potent prolactin (PRL)-releasing factor (PRF) which is distinct from known PRL secretagogues. Posterior pituitary PRF appears to be a small peptide of an unknown cellular origin. Using pituitary stalk-sectioned (SS) male rats, the objectives of this study were: (1) to determine if PRF is transported from the hypothalamus or is synthesized within the pituitary gland, and (2) to compare changes in PRF activity with alterations in the posterior pituitary content of β-endorphin (β-END), oxytocin (OXY), and dopamine (DA). One or two weeks following pituitary SS or sham surgery (SHAM), acid extracts of the posterior pituitary and medial basal hypothalamus (MBH) were analyzed for their hormone content. PRF activity was assessed by determining the stimulation of PRL secretion from perifused anterior pituitary cells, DA was measured by HPLC, and OXY and β-END levels were determined by RIAs. OXY and DA concentrations in the posterior pituitary were reduced more than 95% at both 1 and 2 weeks after SS. PRF activity in the posterior pituitary was significantly reduced by 75 and 90%, 1 and 2 weeks after SS, respectively. In contrast, β-END levels in the posterior pituitary at these times increased 20 and 60%, as compared to SHAM rats. Unlike the posterior pituitary, OXY levels in the MBH increased 123% 1 week following SS, and 1,260% at 2 weeks. These increases may reflect the accumulation of OXY-containing secretory vesicles in the severed nerves. DA concentrations in the MBH showed a biphasic pattern. DA levels were initially decreased by 70%, and then increased, but remained 30% below SHAM levels. The reason for these alterations in DA levels is not clear. It is concluded that: (1) similar to OXY and DA, but unlike β-END, PRF is likely transported from the hypothalamus to the posterior pituitary, and (2) the low levels of PRF activity in the MBH suggest that PRF may be synthesized as a biologically inactive precursor, the amount of PRF in the MBH is too low to detect, or inhibitors of PRL secretion mask the PRF acti
ISSN:0028-3835
DOI:10.1159/000125028
出版商:S. Karger AG
年代:1988
数据来源: Karger
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16. |
Changes in Tuberoinfundibular Dopaminergic Neuron Activity During the Rat Estrous Cycle in Relation to the Prolactin Surge: Alteration by a Mammary Carcinogen |
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Neuroendocrinology,
Volume 48,
Issue 3,
1988,
Page 320-327
Catherine Pasqualini,
Florence Bojda,
Florence Gaudoux,
Bernard Guibert,
Vincent Leviel,
Elisabeth Teissier,
Richard Rips,
Bernard Kerdelhue,
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摘要:
An attempt was made to correlate the physiological or the dimethylbenz(a)anthracene (DMBA)-enhanced serum prolactin (PRL) surge, which occurs in the afternoon of proestrus in female Sprague-Dawley (SD) rats, with physiological or pathological changes in two biochemical estimates of the tuberoinfundibular dopaminergic (TIDA) neuron activity. Dopamine (DA) and dihydroxyphenylacetic acid (DOPAC) concentrations as well as tyrosine hydroxylase (TH) activity were measured in the median eminence (ME) of control or DMBA-pretreated SD rats throughout the estrous cycle in relation to PRL secretion. In both groups of females, while the DA content was fairly constant, the DOPAC content and TH activity in the ME fluctuated markedly throughout the estrous cycle. Thus, in control animals, the DOPAC content, DOPAC/DA ratio and TH activity which were stable on the days of diestrus and morning of proestrus were markedly decreased at noon and early afternoon when serum PRL levels began to rise. Later in the afternoon of proestrus, when serum PRL levels were maximal, there was a marked but transient increase in the DOPAC content and DOPAC/DA ratio as well as a brief surge in TH activity. In the evening of the same day, when serum PRL returned to basal levels, the DOPAC content, DOPAC/DA ratio and TH activity were low. Finally on estrus morning, the DOPAC content, DOPAC/ DA ratio and TH activity increased again to reach the diestrus levels. In DMBA-pretreated females, similar fluctuations in TIDA neuronal activity occurred during the estrous cycle, but the dynamics of these changes was altered: the DOPAC/DA ratio and TH activity first showed a marked increase in the morning of proestrus day, before decreasing dramatically. No surge in TH activity was detectable in the afternoon of proestrus and the increase in the DOPAC/DA ratio was of lesser amplitude than that in the controls. In those females whose PRL levels were still higher than those of controls on the morning of estrus, the second increase in the DOPAC/DA ratio was not observed. These results suggest that the lowering in TIDA neuronal activity on the day of proestrus might explain the outset, but not the termination of the preovulatory PRL surge. The regulation involved in the latter process seems to be particularly impaired by DMBA pretreatment.
ISSN:0028-3835
DOI:10.1159/000125029
出版商:S. Karger AG
年代:1988
数据来源: Karger
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17. |
Announcement |
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Neuroendocrinology,
Volume 48,
Issue 3,
1988,
Page 328-328
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ISSN:0028-3835
DOI:10.1159/000125030
出版商:S. Karger AG
年代:1988
数据来源: Karger
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