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1.
Gen Comp Endocrinol ; 168(2): 293-301, 2010 Sep 01.
Artigo em Inglês | MEDLINE | ID: mdl-20067800

RESUMO

The melanotrope cell in the amphibian pituitary pars intermedia is a model to study fundamental aspects of neuroendocrine integration. They release alpha-melanophore-stimulating hormone (alphaMSH), under the control of a large number of neurochemical signals derived from various brain centers. In Xenopus laevis, most of these signals are produced in the hypothalamic magnocellular nucleus (Mg) and are probably released from neurohemal axon terminals in the pituitary neural lobe, to stimulate alphaMSH-release, causing skin darkening. The presence in the neural lobe of at least eight stimulatory factors implicated in melanotrope cell control has led us to investigate the ultrastructural architecture of this neurohemal organ, with particular attention to the diversity of neurohemal axon terminals and their neurochemical contents. Using regular electron microscopy, we here distinguish six types of neurohemal axon terminal, on the basis of the size, shape and electron-density of their secretory granule contents. Subsequently, we have identified the neurochemical contents of these terminal types by immuno-electron microscopy and antisera raised against not only the 'classical' neurohormones vasotocin and mesotocin but also brain-derived neurotrophic factor, cocaine- and amphetamine-regulated transcript peptide, corticotropin-releasing factor, metenkephalin, pituitary adenylyl cyclase-activating polypeptide, thyrotropin-releasing hormone and urocortin-1. This has revealed that each terminal type possesses a unique set of neurochemical messengers, containing at least four, but in some cases up to eight messengers. These results reveal the potential of the Mg/neural lobe system to release a wide variety of neurochemical messengers in a partly co-ordinated and partly differential way to control melanotrope cell activity as well as ion and water balance regulatory organs, in response to various, continuously changing, environmental stimuli.


Assuntos
Hipófise/metabolismo , Hipófise/ultraestrutura , Xenopus laevis/metabolismo , Animais , Microscopia Imunoeletrônica , Vesículas Secretórias/metabolismo , Vesículas Secretórias/ultraestrutura
2.
Ann N Y Acad Sci ; 1163: 292-5, 2009 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-19456350

RESUMO

We showed the presence of glucocorticoid (GR) and mineralocorticoid (MR) receptors in different populations of Xenopus laevis melanotrope cells and revealed their downregulation (MR) and upregulation (GR) during dark background adaptation. Corticosterone did not affect short-term intracellular calcium dynamics and alpha-melanophore-stimulating hormone secretion, suggesting a role for GR and MR in long-term processes in the melanotropes.


Assuntos
Glucocorticoides/metabolismo , Adeno-Hipófise Parte Intermédia/metabolismo , Receptores de Mineralocorticoides/metabolismo , Xenopus laevis/metabolismo , Animais , Transporte Biológico , Microscopia Imunoeletrônica
3.
Gen Comp Endocrinol ; 164(1): 32-9, 2009 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-19362554

RESUMO

The rodent non-preganglionic Edinger-Westphal nucleus (npEW) is involved in the stress adaptation response. Here we describe the ultrastructural organization of this nucleus in the unchallenged rat, using different tissue fixation and embedding methods, and postembedding immunogold labeling. In this way we have (1) identified Ucn1-immunopositive neurons, (2) described the ultrastructure of these neurons with focus on cell organelles involved in secretion (rough endoplasmic reticulum, Golgi apparatus, secretory granules), (3) demonstrated the subcellular coexistence of Ucn1 with cocaine- and amphetamine-related transcript peptide, and (4) classified various morphological types and configurations of synaptic contact present in the npEW and, specifically, on the npEW-Ucn1 neurons. The data obtained provide the morphological basis for future studies on the plastic effects of acute and chronic stressors as well as feeding conditions specifically affecting the secretory activity of npEW-Ucn1 neurons.


Assuntos
Neurônios/metabolismo , Neurônios/ultraestrutura , Animais , Encéfalo/citologia , Encéfalo/metabolismo , Encéfalo/ultraestrutura , Imuno-Histoquímica , Técnicas In Vitro , Masculino , Microscopia Imunoeletrônica , Fragmentos de Peptídeos/metabolismo , Ratos , Ratos Wistar , Urocortinas/metabolismo
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