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.