IndraLab

Statements



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"BK channel activation with NS-1619 (30 muM) significantly inhibited the amplitude, muscle force, frequency, duration, and tone of the spontaneous phasic and pharmacologically induced DSM contractions from human DSM isolated strips."

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"The inhibitory effect of selective BK channel activation with NS1619 on electrical field stimulation-induced contractions is attenuated in DSM strips isolated from HFD rats."

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"XREF_BIBR, XREF_BIBR, XREF_BIBR, XREF_BIBR, XREF_BIBR On the other hand, well established (such as NS1608, NS8 and NS1619) and novel (such as NS11021) BK channel openers increase BK channel open probability and whole-cell BK currents, causing DSM hyperpolarization and relaxation in various species."

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"27 The Petkov research group proposes the novel hypothesis that BK channels are key determinants of age- and sex related differences in bladder physiology, and therefore changes in BK channel expression, function, or regulation may underlie age and sex specific DSM dysfunction and resultant LUTD."

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"By reducing overall DSM excitability, BK channel activation with NS1619 can significantly diminish spontaneous, pharmacologically induced and nerve evoked contractions."

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"BK channel inhibition with paxilline (1 muM) attenuated the PGE 2 -induced DSM phasic contractions, suggesting that BK channels are involved in the mechanism of PGE 2 -induced DSM contractions."

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"BK channel pharmacological inhibition with IBTX completely blocked the NS1619 induced relaxation of rat DSM confirming NS1619 selectivity for the BK channel."

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"Here, we examined systematically how the BK channel pharmacological activation modulates DSM contractility."