Chronic stress elicits prolonged activation of α‐MSH secretion and subsequent degeneration of melanotroph

Prolonged stress affects homeostasis in various organs and induces stress‐associated disorders. We examined the cellular changes of pituitary gland under the continuous stress condition using a rat model in which rats were kept in a cage filled with water to a height of 1.5 cm for up to 5 days. Amon...

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Veröffentlicht in:Journal of neurochemistry 2009-06, Vol.109 (5), p.1389-1399
Hauptverfasser: Ogawa, Tokiko, Shishioh‐Ikejima, Nobue, Konishi, Hiroyuki, Makino, Tetsuya, Sei, Hiroyoshi, Kiryu‐Seo, Sumiko, Tanaka, Masaaki, Watanabe, Yasuyoshi, Kiyama, Hiroshi
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Sprache:eng
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Zusammenfassung:Prolonged stress affects homeostasis in various organs and induces stress‐associated disorders. We examined the cellular changes of pituitary gland under the continuous stress condition using a rat model in which rats were kept in a cage filled with water to a height of 1.5 cm for up to 5 days. Among the pituitary hormone mRNAs, proopiomelanocortin mRNA was up‐regulated specifically in the intermediate lobe (IL) of this rat model. Additionally, the peripheral blood levels of α‐melanocyte stimulating hormone (α‐MSH), a major product of proopiomelanocortin in IL were increased. The α‐MSH secreting cells, melanotrophs, showed a markedly developed endoplasmic reticulum and Golgi apparatus in the early phase of the experiment. Subsequent continuous stress caused remarkable dilation of the endoplasmic reticulum, disruption of the Golgi structure, and the degeneration of some melanotrophs. In addition the dopaminergic nerve fibers from hypothalamus were markedly decreased in IL. A dopamine antagonist elicited the similar morphologic changes of melanotroph in normal rat. These findings suggest that prolonged stress suppressed hypothalamus‐derived dopamine release in IL, which elicited over‐secretion of α‐MSH from the melanotrophs. The present study also suggests that prolonged hyperactivation of endocrine cells could lead to disorder of secretion mechanisms and eventual degeneration.
ISSN:0022-3042
1471-4159
DOI:10.1111/j.1471-4159.2009.06057.x