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- W2105424924 abstract "In severe myocardial ischemia, histamine 3 (H<sub>3</sub>) receptor activation affords cardioprotection by preventing excessive norepinephrine release and arrhythmias; pivotal to this action is the inhibition of neuronal Na<sup>+</sup>/H<sup>+</sup> exchanger (NHE). Conversely, angiotensin II, formed locally by mast cell-derived renin, stimulates NHE via angiotensin II type 1 (AT<sub>1</sub>) receptors, facilitating norepinephrine release and arrhythmias. Thus, ischemic dysfunction may depend on a balance between the NHE-modulating effects of H<sub>3</sub> receptors and AT<sub>1</sub> receptors. The purpose of this investigation was therefore to elucidate the H<sub>3</sub>/AT<sub>1</sub> receptor interaction in myocardial ischemia/reperfusion. We found that H<sub>3</sub> receptor blockade with clobenpropit increased norepinephrine overflow and arrhythmias in Langendorff-perfused guinea pig hearts subjected to ischemia/reperfusion. This coincided with increased neuronal AT<sub>1</sub> receptor expression. NHE inhibition with cariporide prevented both increases in norepinephrine release and AT<sub>1</sub> receptor expression. Moreover, norepinephrine release and AT<sub>1</sub> receptor expression were increased by the nitric oxide (NO) synthase inhibitor <i>N</i><sup>G</sup>-methyl-l-arginine and the protein kinase C activator phorbol myristate acetate. H<sub>3</sub> receptor activation in differentiated sympathetic neuron-like PC12 cells permanently transfected with H<sub>3</sub> receptor cDNA caused a decrease in protein kinase C activity and AT<sub>1</sub> receptor protein abundance. Collectively, our findings suggest that neuronal H<sub>3</sub> receptor activation inhibits NHE by diminishing protein kinase C activity. Reduced NHE activity sequentially causes intracellular acidification, increased NO synthesis, and diminished AT<sub>1</sub> receptor expression. Thus, H<sub>3</sub> receptor-mediated NHE inhibition in ischemia/reperfusion not only opposes the angiotensin II-induced stimulation of NHE in cardiac sympathetic neurons, but also down-regulates AT<sub>1</sub> receptor expression. Cardioprotection ultimately results from the combined attenuation of angiotensin II and norepinephrine effects and alleviation of arrhythmias." @default.
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- W2105424924 date "2011-10-19" @default.
- W2105424924 modified "2023-10-17" @default.
- W2105424924 title "Histamine 3 Receptor Activation Reduces the Expression of Neuronal Angiotensin II Type 1 Receptors in the Heart" @default.
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- W2105424924 doi "https://doi.org/10.1124/jpet.111.187765" @default.
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