Aims: 24‐Hydroxycholesterol (24HC) is the main brain cholesterol metabolite, which level in the circulation is significantly changed under physiological and pathological conditions. Here, we have studied the effect of 24HC… Click to show full abstract
Aims: 24‐Hydroxycholesterol (24HC) is the main brain cholesterol metabolite, which level in the circulation is significantly changed under physiological and pathological conditions. Here, we have studied the effect of 24HC on the inotropic responses to &bgr;‐adrenoceptor (AR) stimulation. Main methods: Electrical stimulation‐evoked contractions were recorded in isolated atria from mice. Fluorescent dyes, Fluo‐4 and DAF‐FM, were used for estimation of Ca2+ transient and NO production, respectively. Key findings: We revealed that 24HC in the submicromolar range attenuated &bgr;‐AR‐induced positive inotropy in isolated atria. This was accompanied by a decrease in Ca2+ transient and unchanged nitric oxide (NO) production. However, &bgr;1‐AR‐induced positive inotropy and enhancement of Ca2+ transient were increased by 24HC due to suppression of NO production. Only &bgr;2‐AR‐dependent inotropy and enhancement of Ca2+ transient were decreased by 24HC in a NO‐independent manner. Inhibition of phosphodiesterase (PDE) suppressed effect of 24HC on &bgr;2‐AR‐dependent contractility as well as on non‐subtype specific &bgr;‐AR activation. Moreover, 24HC counteracted positive inopropic action of PDE inhibitors, IBMX and rolipam. Thus, 24HC modulates the effects of &bgr;1‐ and &bgr;2‐AR stimulation via different mechanisms linked with change in activity of NO synthase or PDE, respectively. Under conditions of non‐selective activation of &bgr;‐ARs, the depressant effect of 24HC related with &bgr;2‐AR‐dependent signaling dominates. Significance: We suggest that 24HC could serve as a modulator of atrial &bgr;‐AR signaling, contributing to regulation of contractility. Graphical abstract Figure. No caption available. HighlightsWe studied alteration in responses to &bgr;‐adrenoceptor stimulation in the mice atria.24‐Hydroxycholesterol suppressed effects of &bgr;‐adrenoceptors on contractility and [Ca2+]in.The oxysterol affected responses to &bgr;1 and &bgr;2‐adrenoceptor activation in different ways.The mechanisms of oxysterol effects were dependent on NO synthase and phosphodiesterase.24‐Hydroxycholesterol is a potential modulator of &bgr;‐adrenoceptor dependent signaling.
               
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