Matches in SemOpenAlex for { <https://semopenalex.org/work/W2149074405> ?p ?o ?g. }
- W2149074405 endingPage "805" @default.
- W2149074405 startingPage "797" @default.
- W2149074405 abstract "The vasoactive peptides angiotensin II (Ang II) and endothelin-1 (ET-1) have been implicated in cardiac hypertrophy. This study investigates Ang II and ET-1 effects on intracellular free calcium concentration and the receptor subtype through which agonist-induced calcium responses are mediated in isolated cardiomyocytes and fibroblasts from hypertrophied hearts of spontaneously hypertensive rats (SHR). We measured intracellular free calcium concentration by fura 2 methodology and determined receptor status by radioligand binding assays. Ang II (10 −12 to 10 −7 mol/L) had no effect on cardiomyocyte calcium levels in control Wistar-Kyoto rats but significantly increased ( P< .01) intracellular free calcium concentration in a dose-dependent manner in cardiomyocytes from SHR. Ang II total and specific binding were increased ( P< .05) in SHR cardiomyocytes. Calcium responses elicited by 10 −7 to 10 −5 mol/L Ang II were significantly reduced ( P< .01) in SHR fibroblasts despite no significant change in Ang II receptor density. The angiotensin type 1 receptor blocker losartan (1 μmol/L) blocked Ang II–stimulated calcium transients, whereas the angiotensin type 2 receptor blocker PD 123319 had no effect. ET-1– and sarafotoxin S6c–induced calcium responses in cardiomyocytes and fibroblasts were not different between hypertensive and control groups. In conclusion, Ang II and ET-1 elicit distinct and differential responses in a cell-specific manner in cardiomyocytes and fibroblasts from hypertrophied hearts of SHR. Whereas Ang II–mediated effects, which are elicited via angiotensin type 1 receptors, are detectable in cardiomyocytes from SHR, responses to Ang II are blunted in fibroblasts from SHR, and ET-1–related actions are similar in cells from both rat groups. Stimulation of cardiomyocytes by Ang II in hypertrophied hearts associated with pressure overload in genetic hypertension suggests that Ang II could modulate the function of cardiomyocytes of SHR but not those of Wistar-Kyoto rats, whereas cardiac actions of ET-1 do not change with the development of hypertension." @default.
- W2149074405 created "2016-06-24" @default.
- W2149074405 creator A5020577597 @default.
- W2149074405 creator A5046910928 @default.
- W2149074405 creator A5065121704 @default.
- W2149074405 creator A5083816500 @default.
- W2149074405 date "1996-11-01" @default.
- W2149074405 modified "2023-10-16" @default.
- W2149074405 title "Intracellular Ca <sup>2+</sup> Modulation by Angiotensin II and Endothelin-1 in Cardiomyocytes and Fibroblasts From Hypertrophied Hearts of Spontaneously Hypertensive Rats" @default.
- W2149074405 cites W1583624289 @default.
- W2149074405 cites W1965078731 @default.
- W2149074405 cites W1973805487 @default.
- W2149074405 cites W1981539578 @default.
- W2149074405 cites W2044261018 @default.
- W2149074405 cites W2045818769 @default.
- W2149074405 cites W2046259108 @default.
- W2149074405 cites W2055703429 @default.
- W2149074405 cites W2060499559 @default.
- W2149074405 cites W2091581734 @default.
- W2149074405 cites W2105763003 @default.
- W2149074405 cites W2108915868 @default.
- W2149074405 cites W2109591901 @default.
- W2149074405 cites W2120422681 @default.
- W2149074405 cites W2127088794 @default.
- W2149074405 cites W2141260882 @default.
- W2149074405 cites W2154890342 @default.
- W2149074405 cites W2170838818 @default.
- W2149074405 cites W2276591666 @default.
- W2149074405 cites W2309341672 @default.
- W2149074405 cites W2321591535 @default.
- W2149074405 cites W2407401749 @default.
- W2149074405 cites W2409305849 @default.
- W2149074405 cites W4231365974 @default.
- W2149074405 doi "https://doi.org/10.1161/01.hyp.28.5.797" @default.
- W2149074405 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/8901826" @default.
- W2149074405 hasPublicationYear "1996" @default.
- W2149074405 type Work @default.
- W2149074405 sameAs 2149074405 @default.
- W2149074405 citedByCount "35" @default.
- W2149074405 countsByYear W21490744052013 @default.
- W2149074405 countsByYear W21490744052017 @default.
- W2149074405 countsByYear W21490744052018 @default.
- W2149074405 countsByYear W21490744052019 @default.
- W2149074405 crossrefType "journal-article" @default.
- W2149074405 hasAuthorship W2149074405A5020577597 @default.
- W2149074405 hasAuthorship W2149074405A5046910928 @default.
- W2149074405 hasAuthorship W2149074405A5065121704 @default.
- W2149074405 hasAuthorship W2149074405A5083816500 @default.
- W2149074405 hasConcept C104849204 @default.
- W2149074405 hasConcept C126322002 @default.
- W2149074405 hasConcept C134018914 @default.
- W2149074405 hasConcept C144980905 @default.
- W2149074405 hasConcept C149601957 @default.
- W2149074405 hasConcept C170493617 @default.
- W2149074405 hasConcept C181080969 @default.
- W2149074405 hasConcept C181199279 @default.
- W2149074405 hasConcept C185592680 @default.
- W2149074405 hasConcept C198710026 @default.
- W2149074405 hasConcept C2778470358 @default.
- W2149074405 hasConcept C2778938600 @default.
- W2149074405 hasConcept C2780288358 @default.
- W2149074405 hasConcept C2908929049 @default.
- W2149074405 hasConcept C519063684 @default.
- W2149074405 hasConcept C55493867 @default.
- W2149074405 hasConcept C71924100 @default.
- W2149074405 hasConcept C79879829 @default.
- W2149074405 hasConcept C84393581 @default.
- W2149074405 hasConcept C86803240 @default.
- W2149074405 hasConcept C98539663 @default.
- W2149074405 hasConceptScore W2149074405C104849204 @default.
- W2149074405 hasConceptScore W2149074405C126322002 @default.
- W2149074405 hasConceptScore W2149074405C134018914 @default.
- W2149074405 hasConceptScore W2149074405C144980905 @default.
- W2149074405 hasConceptScore W2149074405C149601957 @default.
- W2149074405 hasConceptScore W2149074405C170493617 @default.
- W2149074405 hasConceptScore W2149074405C181080969 @default.
- W2149074405 hasConceptScore W2149074405C181199279 @default.
- W2149074405 hasConceptScore W2149074405C185592680 @default.
- W2149074405 hasConceptScore W2149074405C198710026 @default.
- W2149074405 hasConceptScore W2149074405C2778470358 @default.
- W2149074405 hasConceptScore W2149074405C2778938600 @default.
- W2149074405 hasConceptScore W2149074405C2780288358 @default.
- W2149074405 hasConceptScore W2149074405C2908929049 @default.
- W2149074405 hasConceptScore W2149074405C519063684 @default.
- W2149074405 hasConceptScore W2149074405C55493867 @default.
- W2149074405 hasConceptScore W2149074405C71924100 @default.
- W2149074405 hasConceptScore W2149074405C79879829 @default.
- W2149074405 hasConceptScore W2149074405C84393581 @default.
- W2149074405 hasConceptScore W2149074405C86803240 @default.
- W2149074405 hasConceptScore W2149074405C98539663 @default.
- W2149074405 hasIssue "5" @default.
- W2149074405 hasLocation W21490744051 @default.
- W2149074405 hasLocation W21490744052 @default.
- W2149074405 hasOpenAccess W2149074405 @default.
- W2149074405 hasPrimaryLocation W21490744051 @default.
- W2149074405 hasRelatedWork W169516701 @default.
- W2149074405 hasRelatedWork W1971861764 @default.
- W2149074405 hasRelatedWork W1975305402 @default.