Ultrastructural and neurochemical architecture of the pituitary neural lobe of Xenopus laevis.

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.

Dynamics of glucocorticoid and mineralocorticoid receptors in the Xenopus laevis pituitary pars intermedia.

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.

Ultrastructural and immunocytochemical characterization of the rat non-preganglionic Edinger-Westphal nucleus.

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.