Matches in SemOpenAlex for { <https://semopenalex.org/work/W2038894588> ?p ?o ?g. }
- W2038894588 endingPage "e63386" @default.
- W2038894588 startingPage "e63386" @default.
- W2038894588 abstract "Purpose Anandamide, one of the endocannabinoids, has been reported to exhibit cardioprotective properties, particularly in its ability to limit the damage produced by ischemia reperfusion injury. However, the mechanisms underlying the effect are not well known. This study is to investigate whether anandamide alter Na+/Ca2+ exchanger and the intracellular free Ca2+ concentration ([Ca2+]i). Methods Na+/Ca2+ exchanger current (INCX) was recorded and analysed by using whole-cell patch-clamp technique and [Ca2+]i was measured by loading myocytes with the fluorescent Ca2+ indicator Fura-2/AM. Results We found that INCX was enhanced significantly after perfusion with simulated ischemic external solution; [Ca2+]i was also significantly increased by simulated ischemic solution. The reversal potential of INCX was shifted to negative potentials in simulated ischemic external solution. Anandamide (1–100 nM) failed to affect INCX and [Ca2+]i in normal solution. However, anandamide (1–100 nM) suppressed the increase in INCX in simulated ischemic external solution concentration-dependently and normalized INCX reversal potential. Furthermore, anandamide (100 nM) significantly attenuated the increase in [Ca2+]i in simulated ischemic solution. Blocking CB1 receptors with the specific antagonist AM251 (500 nM) failed to affect the effects of anandamide on INCX and [Ca2+]i in simulated ischemic solution. CB2 receptor antagonist AM630 (100 nM) eliminated the effects of anandamide on INCX and [Ca2+]i in simulated ischemic solution, and CB2 receptor agonist JWH133 (100 nM) simulated the effects of anandamide that suppressed the increase in INCX and [Ca2+]i in simulated ischemic solution. In addition, pretreatment with the Gi/o-specific inhibitor pertussis toxin (PTX, 500 ng/ml) eliminated the effects of anandamide and JWH133 on INCX in simulated ischemic solution. Conclusions Collectively, these findings suggest that anandamide suppresses calcium overload through inhibition of INCX during perfusion with simulated ischemic solution; the effects may be mediated by CB2 receptor via PTX-sensitive Gi/o proteins. This mechanism is importantly involved in the anti-ischemia injury caused by endocannabinoids." @default.
- W2038894588 created "2016-06-24" @default.
- W2038894588 creator A5014942240 @default.
- W2038894588 creator A5018069866 @default.
- W2038894588 creator A5035770690 @default.
- W2038894588 creator A5044417934 @default.
- W2038894588 creator A5057759880 @default.
- W2038894588 date "2013-05-07" @default.
- W2038894588 modified "2023-10-11" @default.
- W2038894588 title "Anandamide Reduces Intracellular Ca2+ Concentration through Suppression of Na+/Ca2+ Exchanger Current in Rat Cardiac Myocytes" @default.
- W2038894588 cites W133992910 @default.
- W2038894588 cites W1685169768 @default.
- W2038894588 cites W1968630563 @default.
- W2038894588 cites W1973615313 @default.
- W2038894588 cites W1976426436 @default.
- W2038894588 cites W1978622737 @default.
- W2038894588 cites W1982569456 @default.
- W2038894588 cites W1986987261 @default.
- W2038894588 cites W1989655446 @default.
- W2038894588 cites W2002538995 @default.
- W2038894588 cites W2006755079 @default.
- W2038894588 cites W2011962376 @default.
- W2038894588 cites W2015614945 @default.
- W2038894588 cites W2018323486 @default.
- W2038894588 cites W2027688921 @default.
- W2038894588 cites W2029860176 @default.
- W2038894588 cites W2030142394 @default.
- W2038894588 cites W2036334874 @default.
- W2038894588 cites W2052715846 @default.
- W2038894588 cites W2053737336 @default.
- W2038894588 cites W2054284283 @default.
- W2038894588 cites W2054301281 @default.
- W2038894588 cites W2055830816 @default.
- W2038894588 cites W2056188558 @default.
- W2038894588 cites W2059690330 @default.
- W2038894588 cites W2063375328 @default.
- W2038894588 cites W2075894678 @default.
- W2038894588 cites W2088139813 @default.
- W2038894588 cites W2088140639 @default.
- W2038894588 cites W2094735736 @default.
- W2038894588 cites W2102941373 @default.
- W2038894588 cites W2103098013 @default.
- W2038894588 cites W2103208173 @default.
- W2038894588 cites W2113299996 @default.
- W2038894588 cites W2113950363 @default.
- W2038894588 cites W2115697402 @default.
- W2038894588 cites W2116884436 @default.
- W2038894588 cites W2117571600 @default.
- W2038894588 cites W2118958095 @default.
- W2038894588 cites W2130625353 @default.
- W2038894588 cites W2138730095 @default.
- W2038894588 cites W2139198003 @default.
- W2038894588 cites W2141260882 @default.
- W2038894588 cites W2158771670 @default.
- W2038894588 cites W2159454962 @default.
- W2038894588 cites W2163132732 @default.
- W2038894588 cites W2181841531 @default.
- W2038894588 cites W2320751042 @default.
- W2038894588 doi "https://doi.org/10.1371/journal.pone.0063386" @default.
- W2038894588 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3646750" @default.
- W2038894588 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/23667607" @default.
- W2038894588 hasPublicationYear "2013" @default.
- W2038894588 type Work @default.
- W2038894588 sameAs 2038894588 @default.
- W2038894588 citedByCount "21" @default.
- W2038894588 countsByYear W20388945882013 @default.
- W2038894588 countsByYear W20388945882014 @default.
- W2038894588 countsByYear W20388945882015 @default.
- W2038894588 countsByYear W20388945882016 @default.
- W2038894588 countsByYear W20388945882017 @default.
- W2038894588 countsByYear W20388945882018 @default.
- W2038894588 countsByYear W20388945882020 @default.
- W2038894588 countsByYear W20388945882021 @default.
- W2038894588 countsByYear W20388945882022 @default.
- W2038894588 crossrefType "journal-article" @default.
- W2038894588 hasAuthorship W2038894588A5014942240 @default.
- W2038894588 hasAuthorship W2038894588A5018069866 @default.
- W2038894588 hasAuthorship W2038894588A5035770690 @default.
- W2038894588 hasAuthorship W2038894588A5044417934 @default.
- W2038894588 hasAuthorship W2038894588A5057759880 @default.
- W2038894588 hasBestOaLocation W20388945881 @default.
- W2038894588 hasConcept C12554922 @default.
- W2038894588 hasConcept C126322002 @default.
- W2038894588 hasConcept C148001335 @default.
- W2038894588 hasConcept C170493617 @default.
- W2038894588 hasConcept C185592680 @default.
- W2038894588 hasConcept C2776158853 @default.
- W2038894588 hasConcept C2778938600 @default.
- W2038894588 hasConcept C2779783865 @default.
- W2038894588 hasConcept C28406088 @default.
- W2038894588 hasConcept C55493867 @default.
- W2038894588 hasConcept C71924100 @default.
- W2038894588 hasConcept C79879829 @default.
- W2038894588 hasConcept C86803240 @default.
- W2038894588 hasConceptScore W2038894588C12554922 @default.
- W2038894588 hasConceptScore W2038894588C126322002 @default.
- W2038894588 hasConceptScore W2038894588C148001335 @default.
- W2038894588 hasConceptScore W2038894588C170493617 @default.