• 제목/요약/키워드: 1,3,4-oxadiazole

검색결과 67건 처리시간 0.026초

석창포에 의한 발기부전 개선 효과 (Effect of Acorus Gramineus on the Relaxation of Corpus Cavernosum Smooth Muscle)

  • 리향;김호태;이재윤;이윤정;신홍균;강대길;이호섭
    • 동의생리병리학회지
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    • 제25권5호
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    • pp.863-869
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    • 2011
  • The aim of the present study is to investigate whether an ethanol extract of Acorus gramineus Soland (EAG) augments penile erection in vitro and in vivo experiment. Preconstructed with phenylephrine (PE) in isolated endothelium-intact rabbit corpus cavernosum, EAG relaxed penile smooth muscle in a dose-dependent manner, which was inhibited by pretreatment with NG-nitro-L-argininemethylester (L-NAME), a nitricoxide synthase inhibitor, and 1H-[1,2,4]-oxadiazole-[4,3-${\alpha}$]-quinoxalin-1-one (ODQ), a soluble guanylylcyclase (sGC) inhibitor, respectively. EAG-induced relaxation was significantly attenuated by pretreatment with tetraethylammonium (TEA), a nonselective $K^+$ channel blocker. EAG increased cGMP levels of the rabbit corpus cavernosum in a concentration-dependent manner without changes in cAMP levels. In addition, EAG caused increase of peak intracavernous pressure (ICP), ICP/MAP ratio and area under the carve (AUC) in SD rats. Taken together, these results suggest that EAG augments penile erection via NO-cGMP system and $K^+$ channels in corpus cavernosum.

선학초 부탄올 추출물의 혈관 이완 효과의 기전에 대한 연구 (Mechanism for the Vascular Relaxation Induced by Butanol Extract of Agrimonia pilosa)

  • 조려화;이준경;조국현;권태오;권지웅;김진숙;손은진;이호섭;강대길
    • 생약학회지
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    • 제37권2호통권145호
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    • pp.67-73
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    • 2006
  • The butanol extracts of Agrimonia pilosa (BAP) induced dose-dependent vascular relaxation of phenylephrine-precontracted aorta, which was abolished by removal of functional endothelium. Pretreatment of the endothelium-intact aortic tissues with $N^G$-nitro-L-arginine methyl ester (L-NAME) and 1H-[1,2,4]-oxadiazole-[$4,3-{\alpha}$]-quinoxalin-1-one(ODQ) inhibited the relaxation induced by BAP. BAP-induced vascular relaxation was also markedly attenuated by addition of verapamiI, while the relaxant effect of BAP was not blocked by indomethacine, glibenclamide, tetraethylammonium (TEA), atropine, or propranolo. In addition, incubation of endothelium-intact aortic rings with BAP increased the vascular production of cGMP. These results suggest that BAP relaxes vascular smooth muscle via endothelium-dependent nitric oxide/cGMP signaling pathway, which may be causally related with L-type $Ca^{2+}$ channels.

담죽엽 추출물의 혈관이완 기전에 대한 연구 (Effect of Lophatherum gracile on the mechanism of vasorelaxation in thoracic aorta)

  • 김혜윰;리향;이윤정;서환호;조남근;강대길;이호섭
    • 대한한의학방제학회지
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    • 제17권2호
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    • pp.175-186
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    • 2009
  • The vasorelaxant effect of an extract of Lophatherum gracile Brongn (ELB) and its possible action mechanism were ascertained in aortic tissues isolated from rats. ELB relaxed endothelium-intact thoracic aorta in a dose-dependent manner. However, the induced vascular relaxation was abolished by removal in endothelium of the thoracic aorta. Pretreatment of endothelium-intact vascular tissues with $N^G$-nitro-L-arginine methyl ester (L-NAME) or 1H-[1,2,4]-oxadiazole-[4,3-$\alpha$]-quinoxalin-1-one (ODQ) significantly inhibited vascular relaxation induced by ELB. Moreover, ELB significantly increased cGMP production in aortic tissues, which was blocked by pretreatment with L-NAME or ODQ. The vasorelaxant effect of ELB was attenuated by tetraethylammonium (TEA), and glibenclamide. ELB-induced vasorelaxation was not blocked by atropine, propranolol, indomethacin, verapamil, and diltiazem. Taken together, the present study demonstrates that ELB dilates vascular smooth muscle via an endothelium-dependent NO-cGMP signaling pathway, which may be at least in part related with the function of $K^+$ channels.

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정향피 추출물의 혈관 이완효과 및 작용기전에 대한 연구 (Study on the Mechanism of Vascular Relaxation Induced by Cortex Caryphylli)

  • 송철민;신선호;정현애;이준경;조려화;강대길;이호섭
    • 동의생리병리학회지
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    • 제20권5호
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    • pp.1166-1173
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    • 2006
  • The aqueous extracts of Cortex Caryophylli (AEC) induced dose-dependent relaxation of phenylephrine-precontracted aorta, which was abolished by removal of functional endothelium. Pretreatment of the endothelium-intact aortic tissues with N$^G$_nitro-L-arginine methyl ester (L-NAME) or 1 H-[1,2,4]-oxadiazole-[4,3-${\alpha}$l-quinoxalin-1-one (ODQ) inhibited the relaxation induced by AEC. AEC-induced vascular relaxations were also markedly attenuated by addition of verapamil, diltiazem and glibenclamide, tetraethylammonium (TEA), respectively, while the relaxation effect of AEC was not blocked by indomethacin, atropine, or propranolol. Moreover, incubation of endothelium-intact aortic rings with AEC increased the production of cGMP. These results suggest that AEC dilates vascular smooth muscle via endothelium-dependent nitric oxide/cGMP signaling, which seems to be causally related with L-type Ca$^{2+}$ and K$^+$ channels.

월견자 물 분획층을 이용한 혈관이완 기전에 관한 연구 (Vascular Relaxation Induced by the Water Soluble Fraction of the Seeds from Oenothera Odorata)

  • 김혜윰;이윤정;윤정주;고민철;한병혁;최은식;박지훈;강대길;이호섭
    • 동의생리병리학회지
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    • 제29권6호
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    • pp.492-497
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    • 2015
  • In the present study, vasorelaxant effect of the extract of seeds of Oenothera odorata (SOO) and its possible mechanism responsible for this effect were examined in vascular tissues isolated from rats. Changes in vascular tension, 3',5'-cyclic monophosphate (cGMP) levels were measured in thoracic aorta rings from rats. Methanol extract of seeds of Oenothera odorata relaxed endothelium-intact thoracic aorta in a dose-dependent manner. A dose-dependent vascular relaxation was also revealed by treatment of ethylacetate, n-butanol, and H2O (aqua extract of seeds of Oenothera odorata , ASOO) extracts partitioned from methanol, but not by hexane extract. However, the vascular relaxation induced by ASOO were abolished by removal of endothelium of aortic tissues. Pretreatment of the endothelium-intact vascular tissues with NG-nitro-L-arginine methyl ester (L-NAME) or 1H-[1,2,4]-oxadiazole-[4,3-α]-quinoxalin-1- one (ODQ) significantly inhibited vascular relaxation induced by ASOO. Moreover, incubation of endothelium-intact aortic rings with ASOO increased the production of cGMP. However, ASOO-induced increases in cGMP production were blocked by pretreatment with L-NAME or ODQ. The vasorelaxant effect of ASOO was attenuated by tetraethylammonium (TEA), 4-aminopyridine, and glibenclamide attenuated. On the other hand, the ASOO-induced vasorelaxation was not blocked by verapamil, and diltiazem. Taken together, the present study demonstrates that ASOO dilate vascular smooth muscle via endothelium-dependent NO-cGMP signaling pathway, which may be closely related with the function of K+ channels.

벼와 피에 대한 Azimsulfuron의 작용성(作用性)에 미치는 혼합제초제(混合除草劑)의 영향(影響) (Effect of Mixed Herbicides on Phytotoxicity of Azimsulfuron in Rice and Barnyardgrass)

  • 전재철;마상용;김성은
    • 한국잡초학회지
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    • 제15권3호
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    • pp.232-237
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    • 1995
  • 일년생(一年生) 방제용(防除用) 제초제(除草劑) 8종과 혼합(混合)된 azimsulfuron의 벼와 피의 지상부(地上部) 및 뿌리 생육(生育)에 끼치는 영향(影響)을 조사(調査)하였다. 벼 지상부는 일년생(一年生) 제초제(除草劑) 혼합처리(混合處理)가 azimsulfuron 단독(單獨) 처리(處理)보다 큰 생육억제(生育抑制) 효과(效果)를 나타내었으나, 어느 경우에도 약해(藥害) 경감(經減) 효과(效果)는 없었다. 벼 뿌리에 대한 약해 경감 효과는 10ppm 이상의 azimsulfuron에 혼합(混合)된 dimepiperate, molinate 및 dymron 에서만 나타났다. 벼 지상부(地上部) 및 뿌리의 생육억제(生育抑制) 효과(效果)는 직쇄상(直鎖狀) 탄화수소(炭化水素) 치환체(置換體)인 esprocarb나 thiobencarb의 혼합(混合)이 환상(環狀) 탄화수소(炭化水素) 치환체(置換體)인 dimepiperate나 molinate의 혼합(混合)에서 보다 크게 나타났다. Azimsulfuron에 대한 일년생(一年生) 제초제(除草劑)의 혼합(混合)으로 피의 지상부(地上部) 및 뿌리 생육억제(生育抑制) 는 azimsulfuron 단독(單獨) 처리(處理)에 비하여 크게 증대(增大) 되었다.

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장미근(薔薇根) 메탄올 추출물의 혈관이완 기전에 대한 연구 (Study on the Mechanism of Vascular Relaxation of Methanol Extract of Rose multiflora Radix)

  • 김대중;조남근;이준경;조려화;이혁;안준석;엄재연;조규원;나한일;경은호;강대길;이호섭
    • 동의생리병리학회지
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    • 제21권2호
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    • pp.408-413
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    • 2007
  • Vascular tone plays an important role in the regulation of blood pressure. In the present study, the methanol extract of Rosae multiflora Radix (MRM) induced dose-dependent relaxation of phenylephrine-precontracted aorta, which was abolished by removal of functional endothelium. Pretreatment of the endothelium-intact aortic tissues with $N^G$-nitro-L-arginine methly ester (L-NAME) or 1H-[1,2,4]-oxadiazole-[4,3-${\alpha}$]-quinoxalin-1-one (ODQ) inhibited the relaxation induced by MRM, respectively. But, the relaxation effect of MRM was not blocked by indomethacine, glibenclamide, tetraethylammonium (TEA), verapamil, diltiazem, atropine, and propranolol, respectively. Moreover, incubation of endothelium-intact aortic rings with MRM increased the production of cGMP. Taken together, the present results suggest that MRM relaxes vascular smooth muscle via endothelium-dependent nitric oxide/cGMP signaling. These results would be useful for further study to MRM on animal models with cardiovascular diseases.