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In vivo administered reserpine increases piecemeal degranulation in rat adrenal chromaffin cells

BELLONI, A.
•
NICO, B.
•
NUSSDORFER, G.
altro
CRIVELLATO, Enrico
2006
  • journal article

Periodico
ANATOMICAL RECORD. PART A, DISCOVERIES IN MOLECULAR, CELLULAR, AND EVOLUTIONARY BIOLOGY
Abstract
The effects of the amine-depletory agent reserpine have been evaluated by transmission electron microscopy in chromaffin cells of the rat adrenal glands. The drug has been injected intraperitoneally in the animals at a dose of 0.5 mg/kg body weight in two administrations at 24-hr interval. The observed ultrastructural changes closely reminded of piecemeal degranulation (PMD), a slow and long-lasting secretory process previously described in normal and tumor pheochromocytes. Both adrenaline- and noradrenaline-storing cells presented the following microscopic features: high granule polymorphism, due to coexistence in the same cell of normal resting granules, granules with partially mobilized components, and large empty containers; absence of granule fusion; characteristic "haloed" pattern of residual secretory contents; great amount of 30-150 nm diameter, membrane-bound, electron-dense and -lucent vesicles, free in the cytoplasm or attached to granules; and multiple vesicles budding from the granule-limiting membranes. Morphometric analysis revealed that the frequency of all these microscopic parameters was found to be significantly increased in adrenal chromaffin cells from reserpinized rats in comparison to cells from control animals. These data suggest that reserpine, besides blocking the inward transport of catecholamines in chromaffin granules, might also stimulate a complex secretory reaction, which shares many common passages with bona fide PMD.
DOI
10.1002/ar.a.20280
WOS
WOS:000236216600008
Archivio
http://hdl.handle.net/11390/880321
info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-33645033798
Diritti
closed access
Scopus© citazioni
8
Data di acquisizione
Jun 14, 2022
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Web of Science© citazioni
7
Data di acquisizione
Mar 19, 2024
Visualizzazioni
1
Data di acquisizione
Apr 19, 2024
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