Matches in SemOpenAlex for { <https://semopenalex.org/work/W2077882709> ?p ?o ?g. }
- W2077882709 endingPage "192" @default.
- W2077882709 startingPage "180" @default.
- W2077882709 abstract "Enhanced epinephrine secretion from adrenal chromaffin cells (ACCs) is an important homeostatic response to severe systemic inflammation during sepsis. Evidence suggests that increased activation of ACCs by preganglionic sympathetic neurons and direct alterations in ACC function contribute to this response. However, the direct effects of sepsis on ACC function have yet to be characterized. We hypothesized that sepsis enhances epinephrine secretion from ACCs by increasing intracellular Ca2+ signaling. Plasma epinephrine concentration was increased 5-fold in the lipopolysaccharide-induced endotoxemia model of sepsis compared with saline-treated control mice. Endotoxemia significantly enhanced stimulus-evoked epinephrine secretion from isolated ACCs in vitro. Carbon fiber amperometry revealed an increase in the number of secretory events during endotoxemia, without significant changes in spike amplitude, half-width, or quantal content. ACCs isolated up to 12 hours after the induction of endotoxemia exhibited larger stimulus-evoked Ca2+ transients compared with controls. Similarly, ACCs from cecal ligation and puncture mice also exhibited enhanced Ca2+ signaling. Although sepsis did not significantly affect ACC excitability or voltage-gated Ca2+ currents, a 2-fold increase in caffeine (10 mM)-stimulated Ca2+ transients was observed during endotoxemia. Depletion of endoplasmic reticulum Ca2+ stores using cyclopiazonic acid (10 μM) abolished the effects of endotoxemia on catecholamine secretion from ACCs. These findings suggest that sepsis directly enhances catecholamine secretion from ACCs through an increase in Ca2+ release from the endoplasmic reticulum. These alterations in ACC function are likely to amplify the effects of increased preganglionic sympathetic neuron activity to further enhance epinephrine levels during sepsis." @default.
- W2077882709 created "2016-06-24" @default.
- W2077882709 creator A5041329927 @default.
- W2077882709 creator A5055953572 @default.
- W2077882709 date "2014-01-01" @default.
- W2077882709 modified "2023-09-26" @default.
- W2077882709 title "Endotoxemia Enhances Catecholamine Secretion From Male Mouse Adrenal Chromaffin Cells Through an Increase In Ca2+ Release From the Endoplasmic Reticulum" @default.
- W2077882709 cites W1518494023 @default.
- W2077882709 cites W1571332834 @default.
- W2077882709 cites W1606631580 @default.
- W2077882709 cites W1820594263 @default.
- W2077882709 cites W1943804967 @default.
- W2077882709 cites W1963975982 @default.
- W2077882709 cites W1965489387 @default.
- W2077882709 cites W1966670564 @default.
- W2077882709 cites W1966795480 @default.
- W2077882709 cites W1966886300 @default.
- W2077882709 cites W1972329720 @default.
- W2077882709 cites W1972721072 @default.
- W2077882709 cites W1977433566 @default.
- W2077882709 cites W1977484354 @default.
- W2077882709 cites W1980723571 @default.
- W2077882709 cites W1981409881 @default.
- W2077882709 cites W1981860055 @default.
- W2077882709 cites W1983714985 @default.
- W2077882709 cites W1997116271 @default.
- W2077882709 cites W2002422493 @default.
- W2077882709 cites W2004960843 @default.
- W2077882709 cites W2006926451 @default.
- W2077882709 cites W2007203396 @default.
- W2077882709 cites W2009945632 @default.
- W2077882709 cites W2012458221 @default.
- W2077882709 cites W2013324232 @default.
- W2077882709 cites W2013922264 @default.
- W2077882709 cites W2017780941 @default.
- W2077882709 cites W2019021669 @default.
- W2077882709 cites W2023945291 @default.
- W2077882709 cites W2029216493 @default.
- W2077882709 cites W2035433014 @default.
- W2077882709 cites W2036244056 @default.
- W2077882709 cites W2040113487 @default.
- W2077882709 cites W2053958174 @default.
- W2077882709 cites W2062040725 @default.
- W2077882709 cites W2062135327 @default.
- W2077882709 cites W2063596141 @default.
- W2077882709 cites W2076833993 @default.
- W2077882709 cites W2077438176 @default.
- W2077882709 cites W2080954023 @default.
- W2077882709 cites W2086528578 @default.
- W2077882709 cites W2087817212 @default.
- W2077882709 cites W2088407436 @default.
- W2077882709 cites W2092134407 @default.
- W2077882709 cites W2093057855 @default.
- W2077882709 cites W2094207502 @default.
- W2077882709 cites W2095853585 @default.
- W2077882709 cites W2096324267 @default.
- W2077882709 cites W2096458210 @default.
- W2077882709 cites W2098635427 @default.
- W2077882709 cites W2110841019 @default.
- W2077882709 cites W2112719571 @default.
- W2077882709 cites W2113076389 @default.
- W2077882709 cites W2114361822 @default.
- W2077882709 cites W2116232103 @default.
- W2077882709 cites W2116562969 @default.
- W2077882709 cites W2116884014 @default.
- W2077882709 cites W2123967696 @default.
- W2077882709 cites W2125605921 @default.
- W2077882709 cites W2131737428 @default.
- W2077882709 cites W2139951075 @default.
- W2077882709 cites W2146174593 @default.
- W2077882709 cites W2152955526 @default.
- W2077882709 cites W2156573479 @default.
- W2077882709 cites W2160721095 @default.
- W2077882709 cites W2170568009 @default.
- W2077882709 cites W2171244089 @default.
- W2077882709 cites W2317548247 @default.
- W2077882709 cites W2324129500 @default.
- W2077882709 cites W2406476677 @default.
- W2077882709 cites W2427683182 @default.
- W2077882709 cites W3017100980 @default.
- W2077882709 doi "https://doi.org/10.1210/en.2013-1623" @default.
- W2077882709 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/24169560" @default.
- W2077882709 hasPublicationYear "2014" @default.
- W2077882709 type Work @default.
- W2077882709 sameAs 2077882709 @default.
- W2077882709 citedByCount "10" @default.
- W2077882709 countsByYear W20778827092014 @default.
- W2077882709 countsByYear W20778827092015 @default.
- W2077882709 countsByYear W20778827092016 @default.
- W2077882709 countsByYear W20778827092017 @default.
- W2077882709 countsByYear W20778827092020 @default.
- W2077882709 countsByYear W20778827092022 @default.
- W2077882709 crossrefType "journal-article" @default.
- W2077882709 hasAuthorship W2077882709A5041329927 @default.
- W2077882709 hasAuthorship W2077882709A5055953572 @default.
- W2077882709 hasBestOaLocation W20778827091 @default.
- W2077882709 hasConcept C126322002 @default.
- W2077882709 hasConcept C134018914 @default.