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In vivo effect of dopamine antagonists on melanocyte-stimulating hormone cells of the goldfish (Carassius auratus L.) pituitary.

作者信息

Olivereau M, Olivereau J M, Lambert J F

机构信息

Laboratoire de Physiologie, Institut Océanographique, Paris, France.

出版信息

Gen Comp Endocrinol. 1987 Oct;68(1):12-8. doi: 10.1016/0016-6480(87)90054-2.

DOI:10.1016/0016-6480(87)90054-2
PMID:3666418
Abstract

Young goldfish were injected with three dopaminergic antagonists, pimozide, sulpiride, and domperidone, for 5 (low dose) and 7 days (higher dose). Cytological and immunocytochemical techniques using anti-alpha-melanocyte-stimulating hormone (MSH) serum were applied to the pituitary. MSH cells in the three treated groups showed a decrease in immunoreactive cytoplasmic granules, a significant nuclear hypertrophy, and, after 7 days, a cellular enlargement. The nucleolus and the lamellar endoplasmic reticulum were more developed and some mitotic figures occurred. Erythrophores and occasional melanophores were in a stage of maximal dispersion. These changes were not apparent in the solvent-injected controls. The responses to the three blockers of dopaminergic receptors were similar. These data suggest that MSH release seems to be under a dopaminergic inhibitory control in the goldfish. The other cell type of the pars intermedia (PAS-positive and calcium-sensitive in the goldfish) was not clearly affected by the three drugs.

摘要

相似文献

1
In vivo effect of dopamine antagonists on melanocyte-stimulating hormone cells of the goldfish (Carassius auratus L.) pituitary.
Gen Comp Endocrinol. 1987 Oct;68(1):12-8. doi: 10.1016/0016-6480(87)90054-2.
2
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Dopamine inhibition of gonadotropin and alpha-melanocyte-stimulating hormone release in vitro from the pituitary of the goldfish (Carassius auratus).多巴胺对金鱼(Carassius auratus)垂体在体外释放促性腺激素和α-黑素细胞刺激素的抑制作用。
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[Melanotropic hormone of goldfish (Carassius auratus L.): radioimmunologic comparison with synthetic alpha-MSH].[金鱼(Carassius auratus L.)的促黑素细胞激素:与合成α-促黑素细胞激素的放射免疫比较]
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J Physiol. 1986 Jan;370:381-93. doi: 10.1113/jphysiol.1986.sp015940.

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