Korean J Physiol Pharmacol.  1997 Dec;1(6):759-767.

In vitro pharmacological characteristics of SKP-450, a novel K+ channel opener, in non-vascular smooth muscles in comparison with levcromakalim

Affiliations
  • 1 Department of Pharmacol., Coll. Med., Pusan Natl. University, Pusan 602-739 South Korea.

Abstract

In the present study, we characterized the non-vascular smooth muscle relaxant effects of a novel benzoyran derivative, SKP-450 (2-(2"(1",3"-dioxolone)-2-methyl-4-(2'-oxo-1'-pyrrolidinyl)-6-nitro- 2H-1-benzopyran) and its metabolite, SKP-310, in comparison with levcromakalim (LCRK). In the rat stomach fundus, the spontaneous motility stimulated by 10-6.5 M bethanechol was completely eliminated not only by 10(-7) M SKP-450 but also by 10(-6) M LCRK, which were blocked by 10(-6) M glibenclamide. The inhibitory effect of SKP-450 (pD2, 3.94 +/- 0.66) was much less than LCRK (pD2, 5.73 +/- 0.38, P < 0.05). In the bethanechol (10(-6.5) M)-stimulated urinary bladder, the tonus was decreased in association with elimination of spontaneous motility by 10(-7) M SKP-450 and 10-6 M LCRK (pD2, 6.77 +/- 0.06) (P < 0.05), which were inhibitable by 10-6 M glibenclamide. The inhibitory effect of SKP-450 (pD2, 7.66 +/- 0.05) was significantly more potent than that of LCRK (pD2, 6.77 +/- 0.06, P < 0.05). In the rat uterus stimulated by PGF2alpha (10(-7) M), both increased tonus and spontaneous motility were eliminated by 10(-6) M LCRK with slight depression of the tonus, but not by SKP-450 (10(-5) M). The stimulated trachea of guinea-pig by 10-6.5 M bethanechol was moderately suppressed by SKP-450 (10(-6)~10(-5) M) but little by SKP-310. In association with the relaxant effects, SKP-450 (10(-6) M) and LCRK (10(-5) M) caused a significant stimulation of the 86Rb efflux from rat urinary bladder and stomach fundus, which were antagonized by 10(-5) M glibenclamide, whereas the K+ channel openers could not exert a stimulation of the 86Rb efflux from rat uterus. In
conclusion
, it is suggested that SKP-450 exerts potent relaxant effects on the urinary bladder detrusor muscle and duodenum, whereas it shows much less effect on stomach fundus and uterus as contrasted to LCRK.


MeSH Terms

Animals
Bethanechol
Cromakalim*
Depression
Dinoprost
Duodenum
Glyburide
Muscle, Smooth*
Rats
Stomach
Trachea
Urinary Bladder
Uterus
Bethanechol
Cromakalim
Dinoprost
Glyburide
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