pubmed-article:9596807 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:9596807 | lifeskim:mentions | umls-concept:C0036945 | lld:lifeskim |
pubmed-article:9596807 | lifeskim:mentions | umls-concept:C0005615 | lld:lifeskim |
pubmed-article:9596807 | lifeskim:mentions | umls-concept:C0376604 | lld:lifeskim |
pubmed-article:9596807 | lifeskim:mentions | umls-concept:C0001629 | lld:lifeskim |
pubmed-article:9596807 | lifeskim:mentions | umls-concept:C0441712 | lld:lifeskim |
pubmed-article:9596807 | pubmed:dateCreated | 1998-8-6 | lld:pubmed |
pubmed-article:9596807 | pubmed:abstractText | 1. The ability of the fetal adrenal medulla to respond directly to hypoxaemia and secrete catecholamines before the development of a functional innervation of the gland is essential for intrauterine survival. The cellular mechanisms involved in this response to low PO2 are not known, although the presence of oxygen-sensitive K+ channels in carotid body chemoreceptor cells and other sites suggests that these might underlie the chromaffin cell response. 2. Whole-cell patch-clamp techniques have been used to study K+ currents during normoxia and hypoxia in chromaffin cells isolated from the adrenal glands of fetal sheep. 3. Two types of chromaffin cells were observed, those with a fast inactivating K+ current and a larger capacitance and those with a delayed K+ current and smaller capacitance. No cell showed both types of current. The fast inactivating current showed voltage-dependent inactivation and was blocked by 1 mM 4-aminopyridine, characteristics of an IA-type current. The delayed current had two components, a TEA-sensitive, Ca2+-dependent current and a component with the kinetic behaviour of a delayed rectifier. 4. Both types of current were oxygen sensitive. The IA-type current was reduced by 27.4 +/- 3.2 % when the PO2 was reduced to about 15 mmHg. With the delayed current, hypoxia reduced the amplitude by 26.9 +/- 2.4 %, largely by reduction of the Ca2+-dependent component. 5. In the presence of hypoxia, reduction in the amplitude of these oxygen-sensitive K+ currents would increase the frequency and duration of action potentials, leading to increased activation of the L-type Ca2+ channels, influx of Ca2+ and the subsequent secretion of catecholamines. | lld:pubmed |
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pubmed-article:9596807 | pubmed:language | eng | lld:pubmed |
pubmed-article:9596807 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:9596807 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:9596807 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:9596807 | pubmed:month | Jun | lld:pubmed |
pubmed-article:9596807 | pubmed:issn | 0022-3751 | lld:pubmed |
pubmed-article:9596807 | pubmed:author | pubmed-author:RobertsM LML | lld:pubmed |
pubmed-article:9596807 | pubmed:author | pubmed-author:AdamsM BMB | lld:pubmed |
pubmed-article:9596807 | pubmed:author | pubmed-author:McMillenI CIC | lld:pubmed |
pubmed-article:9596807 | pubmed:author | pubmed-author:RychkovG YGY | lld:pubmed |
pubmed-article:9596807 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:9596807 | pubmed:day | 15 | lld:pubmed |
pubmed-article:9596807 | pubmed:volume | 509 ( Pt 3) | lld:pubmed |
pubmed-article:9596807 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:9596807 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:9596807 | pubmed:pagination | 887-93 | lld:pubmed |
pubmed-article:9596807 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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pubmed-article:9596807 | pubmed:year | 1998 | lld:pubmed |
pubmed-article:9596807 | pubmed:articleTitle | Oxygen-sensing mechanisms are present in the chromaffin cells of the sheep adrenal medulla before birth. | lld:pubmed |
pubmed-article:9596807 | pubmed:affiliation | Department of Physiology, University of Adelaide, Adelaide 5005, Australia. | lld:pubmed |
pubmed-article:9596807 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:9596807 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
pubmed-article:9596807 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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