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Abstract

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Çϸ鼭 ºÒ¾ÈÁ¤¼º ¹æ±¤¼öÃàÀ» Á¶ÀýÇÏ´Â °ÍÀÌ ¹Ù¶÷Á÷Çѵ¥ Àü¸³¼±ºñ´ëÁõ Ä¡·á¿¡ »ç¿ëÇÏ´Â ¾ËÆÄ
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µéÀº ¹æ±¤ÃⱸÀÇ ºÎºÐ Æó»öÀ¸·Î À¯¹ßµÈ ºÒ¾ÈÁ¤¼º ¹æ±¤¿¡¼­ ¾ËÆÄ-¾Æµå·¹³¯¸° ±æÇ×Á¦ÀÎ
doxazosin, tamsulosin, prazosinµîÀÌ ¹æ±¤¼öÃà ¾ïÁ¦È¿°ú¸¦ ³ªÅ¸³»´ÂÁö¿¡ ´ëÇÏ¿© µ¿¹°½ÇÇèÀ»
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¹ÝÀÀÀ» Á¤»ó±º°ú ºñ±³ÇÏ°íÀÚ ÇÏ¿´´Ù.

Purpose : Our experiments were done to determine the effects of alpha-1-adrenergic
antagonists which have been commonly used in the treatment of BPH against the
partially obstructed detrusor smooth muscle using in-vitro muscle strip study of female
rat bladder.
Materials and Methods : Partial obstruction was created by means of partial ligation
of the proximal urethra in 15 female Sprague-Dawley rats. After 6 weeks of obstruction,
1¡¿0.5§¯ sized each bladder smooth muscle strip was stimulated by field stimulation(FS),
(1-32§Ô) and bethanechol administration(10-7-10-7M). After
the control stimulations, each strip was pre-treated with doxazosin, tamsulosin, prazosin
and atropine for 30 minutes, and then same stimulations were repeated. Seperate strip
was pre-treated by propranolol for 30 minutes, and then was stimulated by
norepinephrine(10-4M) or phenylephrine(10-4M).
Results : After the administration of doxazosin, percent decreases of maximal tension
developed by FS was significantly greater in obstructed(26-50% of the control) than in
normal rats(0-12% of the control)(p<0.05). Field stimulated tension were inhibited more
in normal(32-40%) than in obstructed rats(p<0.05, 1-32§Ô) after the administration of
prazosin. Atropine inhibited field stimulated tension to a greater degree in
normal(73-63%) than in obstructed(27-43%) rats (p<0.01, 1-32§Ô). Complete inhibitory
effects of atropine against bethanechol
stimulation(10-7-10-4M) was achieved at
10-5M in normal rats. In obstructed rats, complete blockage was achieved
at 10-4M of bethanechol. Norepinephrine decreased basal tension both in
normal and obstructed rats. After pre-treatment of propranolol, phenylephrine and
norepinephrine did not show any increase of basal tension.
Conclusions : Our results suggest that changes of adrenoceptors may be the
underlying cause of bladder instability secondary to outflow obstruction as evidenced by
significant inhibition of the tension of the detrusor muscle by alpha-1-adrenoceptor
blocker(doxazosin but not by tamsulosin) onto in obstructed rat bladder. These results
also suggest that non-cholinergic components of bladder contraction are much more in
obstructed than in normal bladder. It also can be said that doxazosin may have
additional effects against bladder instability caused by BPH.

Å°¿öµå

Partial bladder outlet obstruction; Alpha-adrenergic antagonist;

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