Corticotropin‐releasing Factor in the Adrenal Medulla
Division of Endocrinology, Rhode Island Hospital/Brown University, Providence 02902. Annals of the New York Academy of Sciences
(Impact Factor: 4.38).
02/1987; 512(1):115-28. DOI: 10.1111/j.1749-6632.1987.tb24954.x
Immunoreactive and bioactive corticotropin-releasing factor has been identified in the adrenal gland of dogs, rats and humans. Radioimmunoassay and immunohistochemical experiments have clearly demonstrated that localization of the peptide is confined to the adrenal medulla. CRF-containing cells have a characteristic appearance and are often found in close association with blood vessels. Electron microscopic studies suggest that CRF is secreted at blood vessels within the adrenal medullary vasculature. CRF has also been identified in pheochromocytomas. The amount of the peptide made by such tumors is highly variable as the CRF content of pheochromocytomas may be 20 to 100 times higher or lower than that of normal adrenal tissue. The pathophysiological importance of CRF in pheochromocytomas is unknown. Excessive secretion of the peptide into the peripheral circulation may cause prolonged activation of the pituitary adrenal axis. The peptide may also act within the tumor, although its role remains obscure. Studies on chronically cannulated, awake dogs have shown that CRF is secreted into adrenal venous blood. A gradient exists between adrenal venous and peripheral arterial blood, as CRF is undetectable peripherally under resting conditions. Hemorrhage, a hemodynamic stimulus known to activate a sympathetic adrenal response, increases the CRF secretory rate. The time course of CRF secretion in response to this stimulus parallels that of epinephrine secretion. The physiological significance of adrenal medullary CRF remains to be determined. Although CRF has been shown to affect catecholamine secretion, the peptide appears to be only a weak secretagogue for catecholamines. We suggest that CRF may affect local blood flow within the adrenal medulla and may modify catecholamine secretory rates via this mechanism. The localization of CRF cells in close apposition to blood vessels supports this hypothesis.
Available from: Mark O. Huising
- "The adrenal medulla in particular produces and contains many neurotransmitters and peptide hormones other than CRF, such as neuropeptide Y, serotonin (5-HT), and vasoactive intestinal peptide; the presence has been established, but the functions are incompletely understood (Nussdorfer 1996, Ehrhart-Bornstein et al. 1998). CRF is found exclusively in a subpopulation of medullary chromaffin cells (Hashimoto et al. 1984, Suda et al. 1984, Bruhn et al. 1987a,b, Minamino et al. 1988). Moreover, direct effects of CRF, independent of HPA-axis activation, have been demonstrated on adrenocortical steroid release (Bornstein et al. 1990, Jones & Edwards 1992, van Oers et al. 1992, Nussdorfer 1996). "
[Show abstract] [Hide abstract]
ABSTRACT: Corticotropin-releasing factor (CRF) plays a central role in the regulation of the stress axis. In mammals, CRF as well as its receptors and its CRF-binding protein (CRF-BP) are expressed in a variety of organs and tissues outside the central nervous system. One of these extrahypothalamic sites is the adrenal gland, where the paracrine actions of adrenal CRF influence cortical steroidogenesis and adrenal blood flow. Although the central role of CRF signaling in the initiation and regulation of the stress response has now been established throughout vertebrates, information about the possible peripheral presence of CRF in earlier vertebrate lineages is scant. We established the expression of CRF, CRF-BP, and the CRF receptor 1 in a panel of peripheral organs of common carp (Cyprinus carpio). Out of all the peripheral organs tested, CRF and CRF-BP are most abundantly expressed in the carp head kidney, the fish equivalent of the mammalian adrenal gland. This expression localizes to chromaffin cells. Furthermore, detectable quantities of CRF are released from the intact head kidney following in vitro stimulation with 8-bromo-cAMP in a superfusion setup. The presence of CRF and CRF-BP within the chromaffin compartment of the head kidney suggests that a pathway homologous to the mammalian intra-adrenal CRF system is present in the head kidney of fish. It follows that such a system to locally fine-tune the outcome of the centrally initiated stress response has been an integral part of the vertebrate endocrine system since the common ancestor of teleostean fishes and mammals.
Journal of Endocrinology 07/2007; 193(3):349-57. DOI:10.1677/JOE-07-0070 · 3.72 Impact Factor
[Show abstract] [Hide abstract]
ABSTRACT: Over the past twenty years, each of the five major hypothalamic releasing or release-inhibiting hormones has been sequenced and its gene structure determined. With the use of molecular biological techniques, such as in situ hybridization, Northern blot analysis or gene constructs for in vitro or in vivo transfection studies—together with “traditional’ neuroendocrinological techniques, such as immunocytochemistry, radio-immunoassay and portal vessel cannulation—investigators have been able to address major issues in neuroendocrine regulation. Several common themes have emerged: messenger RNA expression is uniformly present in neurons that are immunopositive for the specific hypothalamic hormone. Steady state RNA levels within the hypophysiotropic neuron groups are either increased or reduced by changes in specific target hormones that conform to predictions based on previous physiological data. Regulation by the requisite peripheral hormone is exquisitely anatomically specific and is not evident in extrahypophysiotropic regions. Determining the receptor or genetic basis of this specificity is a major focus of current research. Clarifying the apparently lesser role of afferent neural pathways to the hypothalamus in regulating releasing hormone mRNA levels is also an important challenge.
Baillière s Clinical Endocrinology and Metabolism 11/1988; 2(4-2):835-868. DOI:10.1016/S0950-351X(88)80021-1
Annals of the New York Academy of Sciences 02/1990; 597(1 Neurobiology):71-80. DOI:10.1111/j.1749-6632.1990.tb16159.x · 4.38 Impact Factor
Data provided are for informational purposes only. Although carefully collected, accuracy cannot be guaranteed. The impact factor represents a rough estimation of the journal's impact factor and does not reflect the actual current impact factor. Publisher conditions are provided by RoMEO. Differing provisions from the publisher's actual policy or licence agreement may be applicable.