Effect of serotonin on α-melanocyte-stimulating hormone secretion from perifused frog neurointermediate lobe: evidence for the presence of serotonin-containing cells in the frog pars intermedia

1989 ◽  
Vol 122 (1) ◽  
pp. 135-NP ◽  
Author(s):  
M. Lamacz ◽  
M. C. Tonon ◽  
F. Leboulenger ◽  
F. Héry ◽  
S. Idres ◽  
...  
Keyword(s):  
Inhibitory Effect ◽  
Electron Microscopic Level ◽  
Adrenergic Nerve ◽  
Pars Intermedia ◽  
Intermediate Lobe ◽  
Melanocyte Stimulating Hormone ◽  
Neurointermediate Lobe ◽  
Parenchymal Cells ◽  
Ics 205 930 ◽  
Stimulating Hormone

ABSTRACT We have examined the presence of 5-hydroxytryptamine (serotonin; 5-HT) in the intermediate lobe of the frog pituitary and investigated the effect of exogenous 5-HT on α-melanocyte-stimulating hormone (α-MSH) release from the perifused neurointermediate lobe (NIL). Using a specific antiserum against 5-HT, the indirect immunofluorescence technique revealed the presence of 5-HT-like immunoreactivity (5-HT-LI) in discrete cells, generally gathered in small clusters among parenchymal cells, and in numerous neurites surrounding melanotrophic cells. At the electron microscopic level, using a silver-gold intensification procedure, 5-HT-LI was localized in dense-core secretory vesicles within specific pituitary cells which appear to be different from pituitary melanotrophs. Dense accumulation of gold particles was also observed in nerve fibres running between parenchymal cells. A combination of high-performance liquid chromatography analysis and electrochemical detection showed the presence of both 5-HT and its metabolite 5-hydroxyindol acetic acid (5-HIAA) in frog NIL extracts (534 ± 40 and 1245 ± 65 (s.e.m.) pg/mg wet tissue respectively). Administration of graded doses of 5-HT (from 1 to 30 μmol/l) to perifused frog NIL induced a dose-dependent inhibition of α-MSH release. Repeated pulses of 5-HT (10 μmol/l each) induced a reproducible inhibition of α-MSH without any desensitization phenomena. The inhibitory effect of 5-HT was partially blocked by the serotonergic antagonists methysergide and ICS-205-930 (10 μmol/l each). Concomitant administration of methysergide and ICS-205-930 (10 μmol/l each) totally abolished 5-HT-evoked inhibition of α-MSH. Fenfluramine, a releaser of 5-HT, induced a slight but significant reduction of α-MSH secretion. While 5-HT caused a marked inhibition of α-MSH release from intact NIL, 5-HT was devoid of effect on acutely dispersed pars intermedia cells suggesting that 5-HT does not exert a direct action on pituitary melanotrophs. We have examined the effect of specific dopaminergic, GABAergic and α-adrenergic antagonists on 5-HT-induced α-MSH inhibition. We observed that sulpiride and SR 95531 (10 μmol/l each) did not affect the response of NIL to 5-HT while yohimbine (10 μmol/l) suppressed the inhibitory action of 5-HT. Taken together, our results indicate that discrete cells of the frog pars intermedia contain the neurotransmitter 5-HT which may act locally to inhibit α-MSH release. Our data also suggest that the inhibitory effect of 5-HT is mediated via presynaptic stimulation of catecholamine (possibly norepinephrine) release from adrenergic nerve endings terminating in the intermediate lobe of the frog pituitary. Journal of Endocrinology (1989) 122, 135–146

INCORPORATION OF 14C-LABELLED AMINO ACIDS INTO CORTICOTROPHIN-LIKE INTERMEDIATE LOBE PEPTIDE AND α-MELANOCYTE-STIMULATING HORMONE BY THE RAT PITUITARY NEUROINTERMEDIATE LOBE IN VITRO, AND THE IDENTIFICATION OF FOUR NEW PARS INTERMEDIA PEPTIDES

1976 ◽  
Vol 70 (2) ◽  
pp. 197-205 ◽  
Author(s):  
A. P. SCOTT ◽  
P. J. LOWRY ◽  
TJ. B. VAN WIMERSMA GREIDANUS
Keyword(s):  
Amino Acids ◽  
The Other ◽  
Pars Intermedia ◽  
Intermediate Lobe ◽  
Melanocyte Stimulating Hormone ◽  
Neurointermediate Lobe ◽  
Rat Pituitary ◽  
Stimulating Hormone

SUMMARY At least seven radioactive peptides, which fractionated on Biogel P6, were found in rat neurointermediate lobes after incubation for 6 h with [14C]proline. Only three of these could be tentatively identified; one as α-melanocyte-stimulating hormone (α-MSH) and two as forms of corticotrophin-like intermediate lobe peptide (CLIP). One other crossreacted partially with a β-melanocyte-stimulating hormone (β-MSH) antiserum, was acidically charged and eluted on Biogel P6 in roughly the same position as ACTH. The other three peptides showed no resemblance to α-MSH, CLIP, β-MSH or ACTH.

ABILITY OF VARIOUS FACTORS TO OPPOSE THE STIMULATORY EFFECT OF DIBUTYRYL CYCLIC AMP ON THE RELEASE OF MELANOCYTE-STIMULATING HORMONE BY THE RAT PITUITARY IN VITRO

1976 ◽  
Vol 68 (2) ◽  
pp. 283-287 ◽  
Author(s):  
BRIDGET I. BAKER
Keyword(s):  
Cyclic Amp ◽  
Cyclic Gmp ◽  
Inhibitory Effect ◽  
Aminobutyric Acid ◽  
Intermediate Lobe ◽  
Dibutyryl Cyclic Amp ◽  
Melanocyte Stimulating Hormone ◽  
Rat Pituitary ◽  
Stimulating Hormone

SUMMARY Various agents were tested for their ability to oppose the stimulatory effect of dibutyryl cyclic AMP on the release of the melanocyte-stimulating hormone from the rat neuro-intermediate lobe in vitro. Only dopamine exhibited an inhibitory effect; serotonin, γ-aminobutyric acid, tocinoic acid, tocinamide, the tripeptide Pro-Leu-Gly-NH2 and dibutyryl cyclic GMP were all ineffective.

scholarly journals Adrenocorticotrophic and melanocyte-stimulating peptides in the human pituitary

1974 ◽  
Vol 139 (3) ◽  
pp. 593-602 ◽  
Author(s):  
Alexander P. Scott ◽  
Philip J. Lowry
Keyword(s):  
Pars Intermedia ◽  
Intermediate Lobe ◽  
Human Pituitary ◽  
Melanocyte Stimulating Hormone ◽  
Stimulating Hormone

The adrenocorticotrophic and melanocyte-stimulating peptides of the human pituitary were investigated by means of radioimmunoassay, bioassay and physicochemical procedures. Substantial amounts of adrenocorticotrophin and a peptide resembling β-lipotrophin were identified in pituitary extracts, but α-melanocyte-stimulating hormone, β-melanocyte-stimulating hormone and corticotrophin-like intermediate lobe peptide, which have been identified in the pars intermedia of pituitaries from other vertebrates, were not found. The absence of β-melanocyte-stimulating hormone appears to contradict previous chemical and radioimmunological studies. Our results suggest, however, that it is not a natural pituitary peptide but an artefact formed by enzymic degradation of β-lipotrophin during extraction.

THE EFFECT OF INGESTION OF HYPERTONIC SALINE ON THE MELANOCYTE-STIMULATING HORMONE CONTENT AND HISTOLOGY OF THE PARS INTERMEDIA OF THE RAT PITUITARY GLAND

1970 ◽  
Vol 46 (2) ◽  
pp. 201-NP ◽  
Author(s):  
A. HOWE ◽  
A. J. THODY
Keyword(s):  
Control Level ◽  
Pars Intermedia ◽  
Type I ◽  
Melanocyte Stimulating Hormone ◽  
Level Of Activity ◽  
Numerous Type ◽  
Rat Pituitary ◽  
Stimulating Hormone

SUMMARY The changes in the content of melanocyte-stimulating hormone (MSH) and histology of the neuro-intermediate (n.i.) lobe were followed in rats which drank 2% sodium chloride for periods from 1–15 days. The pars intermedia showed a biphasic response. During the initial phase of 1–4 days there was a rapid rise in the MSH content, by 153% in the first day, falling back to control level by 4 days. These fluctuations were paralleled by an increase in the normally small numbers of Type 2 cells and at the same time numerous Type I cells showed hypertrophy and degranulation. After 4 days on saline there was a second rise in the MSH content, which was still evident at 15 days; during this second period the number of Type 2 cells declined to normal levels. The degranulated Type 1 cells also disappeared, most of Type 1 being smaller in size and intensely PAS-positive. After the ingestion of saline it apparently takes several days before the pars intermedia adapts to a new level of activity. The likely significance of these changes and the possibility of a relationship between the pars intermedia and the neurohypophysis are discussed.

DISTRIBUTION OF RADIOACTIVITY IN THE ORGANS OF THE RAT AND MOUSE AFTER INJECTION OF [125I]α-MELANOCYTE-STIMULATING HORMONE

1975 ◽  
Vol 64 (2) ◽  
pp. 237-241 ◽  
Author(s):  
A. DUPONT ◽  
A. J. KASTIN ◽  
F. LABRIE ◽  
G. PELLETIER ◽  
R. PUVIANI ◽  
...  
Keyword(s):  
Pineal Gland ◽  
Direct Measurement ◽  
Whole Body ◽  
Intermediate Lobe ◽  
High Uptake ◽  
Melanocyte Stimulating Hormone ◽  
Whole Body Autoradiography ◽  
Very High ◽  
Stimulating Hormone

SUMMARY The distribution of radioactivity after intrajugular injection of 125Ilabelled α-melanocyte-stimulating hormone (α-MSH) was studied by whole-body autoradiography of the mouse and by direct measurement of radioactivity in individual organs of the rat. Very high uptake of radioactivity in the pineal gland was measured 5 min after the injection of [125I]α-MSH. Lower levels of accumulation of radioactivity were found in the kidney and in the posterior (including intermediate) lobe of the pituitary. High uptake was also found in the thyroid, stomach, and oesophagus. The specificity of uptake of [125I] α-MSH into the pineal and pituitary is suggested by the very low uptake of Na125I into those tissues.

GABA-ergic control of α-Melanocyte-Stimulating Hormone (α-MSH) release by frog neurointermediate lobe in vitro

1986 ◽  
Vol 17 (5) ◽  
pp. 717-723 ◽  
Author(s):  
S. Adjeround ◽  
M.C. Tonon ◽  
M. Lamacz ◽  
E. Leneveu ◽  
M.E. Stoeckel ◽  
...  
Keyword(s):  
Melanocyte Stimulating Hormone ◽  
Neurointermediate Lobe ◽  
Stimulating Hormone
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