• Title/Summary/Keyword: vascular smooth muscle contraction

검색결과 104건 처리시간 0.024초

관상동맥이완과 혈소판응집에 대한 GS283과 GS386의 약리작용기전에 관한 연구 (Pharmacological Mechanism of Action of GS283 and GS386 on Human Platelet and Pig Coronary Artery)

  • 장기철;이회영;이균우;구의본;강영진;이영수
    • Biomolecules & Therapeutics
    • /
    • 제5권3호
    • /
    • pp.239-245
    • /
    • 1997
  • Trimetoquinol (TMQ) and its analogs are known to have thromboxane $A_2$ antagonistic action. We also reported that GS389, chemically similar to TMQ, has competitive antagonistic action in rat aorta and human platelets. In the present study, we investigated the pharmacological characteristics of GS283 and GS 386, analogs of GS389, using vascular smooth muscle, human platelets and rat brain homogenates. In isolated pig coronary artery (PCA), both of GS283 and GS386 relaxed U46619-contracted rings in concentration dependent manner. Pretreatment with several concentrations of GS283 and GS386 shifted the dose-response curves to the right, and reduced of maximum contration dose-dependently. Furthermore, GS283 and GS386 strongly inhibited $Ca^{2+}$ -induced contraction in the PCA. In human platelets, U46619- and A23187-induced platelet aggregation was inhibited by GS283 and GS386, concentration-dependently. Anti-platelet aggregation was related to the compound\`s ability to inhibit ATP release at each stimulation. In rat brain homogenates, receptor-binding assay resulted that both GS283 and GS386 have a relative affinity to $\alpha$-adrenergic receptor. Taken together. we concluded that the mechamism of action of GS283 and GS86 is not related with in TXA$_2$ receptor but concerned with calcium antagonistic action and a-blocking action.n.

  • PDF

봉독약침 후 발생한 Anaphylaxis 에 관한 임상적 연구 (Clinical Study of Anaphylaxis on Bee-Venom Acupuncture)

  • 황유진;이병철
    • Journal of Acupuncture Research
    • /
    • 제17권4호
    • /
    • pp.149-159
    • /
    • 2000
  • Bee-venom Acupucture has good effect on pain control but We may be anxious about the problem of side-effect. Bee-venom components are composed of phospholipase $A_2$, hyaluronidase, melitin, apamin, MCD peptide, citrate and so on. Especially Apamin, MCD peptide and histamine cause severe reacting that is named Anaphylaxis. Anaphylaxis is a clinical syndrome characterized by the acute system reaction of multiple organ systems to an IgE-mediated immunologic mediator release in previously sensitized individuals. Respiratory and dermatologic manifestations are the most commonly expressed clinical features of anaphylaxis, and a majority of anaphylactic reactions initially appear to be localized to these two systems. Anaphylatic reaction of bee-venom are expressed clinically ulticaria, itching sensation, erythema, dizziness, nausea, hypotension and so on. Especially ulticaria and erythema are end points of increased vascular permeability and vasodilatation at the other extreme of the clinical spectrum, Gastrointestinal mucosal edema and smooth muscle contraction can result in cramping abdominal pain, nausea, and vomiting. Therefore, we have observed anaphylatic reaction of bee-venom in 11 patients, who visited WonKwang University Kunpo Oriental Medical Center, treated bee venom. The results were summarized as follows : 1. The patient distribution ratio, in regard to sex, was shown to be 1 : 2.67 for male to females. In regard to age, it was shown that people in their 30's was the most predominant case, followed by people in their 20's, 30's, 50's and 60's, respectively. 2. When Anaphylaxis was occured, it was observed to abnormality of CBC, LFT, IgE, IgG. 3. In regard to patient condition, it was observed that fatigue was most frequent. 4. In regard to the number of times and quantity of bee venom inj., it was observed that anaphylaxis is most frequent at 7-10 times(1.6-2.0cc) 5. In regard to duration of reaction, it was observed that people in their l0min' was most frequent. In disappearing duration of anaphylaxic reaction, The results showed under 60min lcases(9%), 60-120min 7cases(64%) and 180-240min 3cases(27%). 6. In symptoms of anaphylaxis, The results showed hypotension 8cases(19%), itching sensation 7cases(16%), nausea 4cases(9%), erythema 4cases(9%) and dizziness 4cases(9%). In mentality, The results showed drowsy 8case(73%) and alert 3cases(27%). 7. Generally, patients were treated with Avil, Dexa IM and PDS, peniramine, cimetidine, Q-zyme per os after H/S, N/S inj. $O_2$ was supplied according to patient's symptom. In 1 severe case, Dopamine was iv injected.

  • PDF

Sodium nitroprusside와 Forskolin의 Phorbol ester 수축에 대한 혈관이완작용의 기전 (The Vasodilating Mechanism of Sodium Nitroprusside and Forskolin on Phorbol dibutyrate-Induced Contractions in Rat Aorta)

  • 안희열
    • 대한약리학회지
    • /
    • 제31권3호
    • /
    • pp.291-297
    • /
    • 1995
  • 본 연구의 목적은 protein kinase C의 활성물질인 phorbol ester의 수축에 대한 cGMP 및 cAMP의 조절기전을 명확히 하기 위하여 흰쥐의 대동맥을 재료로 실험을 수행하였다. Sodium nitroprusside는 guanylyl cyclase를 활성화시켜 cGMP를, forskolin은 adenylyl cyclase를 활성화시켜서 cAMP를 증가시키는 것으로 보고되어 있으므로 위의 두 약물을 선택하였다. Phorbol ester는 시간경과와 함께 지속적인 수축을 발생하였으며 30분경 안정상태에 도달하였다. 동시에 20-kDa myosin light chain (MLC)의 인산화도 증가하였으며 30분경 최대치를 나타내었다. Sodium nitroprusside와 forskolin은 phorbol ester에 의한 수축을 농도의존적으로 억제하였으나 sodium nitroprusside가 forskolin보다 더욱 민감하게 억제하였다. Phorbol ester는 $^{45}Ca^{2+}$의 유입을 증가시켰고 sodium nitroprusside와 forskolin은 이 증가된 $^{45}Ca^{2+}$을 유의하게 억제하였다. Phorbol ester에 의하여 증가된 MLC의 인산화는 sodium nitroprusside 및 forskolin 각각의 최대농도로 억제되었다. 이상과 같은 결과로 볼때 아마도 cGMP와 cAMP는 phorbol ester에 의한 수축을 $^{45}Ca^{2+}$ 유입억제에 이은 MLC 인산화 억제에 의하여 이완작용을 나타내는 것으로 추측되며 cGMP가 cAMP보다 protein kinase C 매개의 수축조절에 더 중요하게 작용하리라 추측된다.

  • PDF

쥐 대동맥 혈관 내피세포에서 세포 외 $K^+$에 의한 혈관 수축선 조절 기전 (Extracellular $K^+$ Effects on the Mouse Aortic Endothelial Cell Contractility)

  • 안재호;유지영
    • Journal of Chest Surgery
    • /
    • 제36권12호
    • /
    • pp.887-893
    • /
    • 2003
  • 외부 자극에 의해 세포 내 $Ca^{2+}$이 증가하면 $K^{+}$이 유출되는 기전을 통해 세포 외 $K^{+}$이 증가하는데, 이 $K^{+}$ 의 증가가 혈관 수축에 미치는 영향을 규명하고자 쥐 대동맥 혈관내피세포를 이용해 실험을 시행하였다. 대상 및 방법: 세포 외 $K^{+}$ 농도를 증가시키거나, 혈관 내피세포의 제거, nitric oxide 생성 억제제인 L-NAME (N-nitro-L-arginine methyl ester)의 투여, $Na^{+}$- $K^{+}$ pump 억제제인 Ouabain, $Na^{+}$-C $a^{2+}$ exchanger 억제제인 N $i^{2+}$의 투여 등 조건을 달리하며, 막전압고정법을 이용, $Ca^{2+}$ 변화와 여러 이온 전류 변화를 측정해 혈관의 수축성을 알아보았다. 결과: 세포외 $K^{+}$ 농도를 6에서 12 mM 증가시켜도 norepinephrine에 의한 혈관의 수축성에는 변화가 없었고, 12 mM 상으로 증가시키면 평활근이 수축하기 시작하였다. Acetylcholine (ACh)에 의해 유발된 내피세포 의존성 이완은 세포 외 $K^{+}$ 농도를 6에서 12 mM로 증가시키면 억제되었으며, 혈관내피세포를 제거하거나 L-NAME을 투여하는 경우에 ACh에 의한 이완은 일어나지 않았다. 배양한 쥐 대동맥 내피세포에서는 ATP혹은 ACh에 의해 세포 내 $Ca^{2+}$이 증가하였으며, 세포 내 $Ca^{2+}$ 증가가 정점에 이른 후 세포 외 $K^{+}$을 6에서 12 mM로 증가시키면 세포 내 $Ca^{2+}$이 농도 의존적으로 감소하였으나 다시 6 mM로 감소시키면 세포 내 $Ca^{2+}$이 증가하였다. 또한 세포 외 $K^{+}$ 증가에 의한 내피세포 의존성 이완효과는 Ouabain과 N $i^{2+}$에 의하여 억제되었다. 걸론 세포 외 $K^{+}$의 증가는 저항혈관 평활근은 이완시키며, 혈관내피세포 $Ca^{2+}$을 감소시켜 내피세포 의존성 이완을 억제하는데 이는 $Na^{+}$- $K^{+}$ pump와 $Na^{+}$-C $a^{2+}$exchanger를 활성화시켜 일어나는 것으로 생각된다.