• Title/Summary/Keyword: 혈관 수축

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Relation between Expression of Heat Shock Protein 70 and Vascular Contractility of Rat Aorta Treated with Arsenic (Arsenic처리에 따른 흰쥐 혈관의 수축과 heat shock protein 70과의 관계)

  • 권윤정;박태규;김중영
    • Korean Journal of Environmental Biology
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    • v.21 no.3
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    • pp.313-318
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    • 2003
  • Environmental stresses, such as heat shock, alcohol and physiological salt have been shown to induce a group of protein called heat shock protein (HSPs) in various tissues. In this investigation, we studied that arsenic stress would alter contraction of isolated rat aorta and expression of heat shock protein 70 and investigated the relation between expression of HSP 70 and vascular contractility of isolated rat aorta. Rat aorta strips, mounted in organ baths were exposed to 0, 0.5, 1,2 and 4 mM arsonic for 60 min. and 1,3 and 8 hours later tested for contractile response and expression of heat shock protein 70. Contractility of rat aorta were determined by isometric transducer connected to computerized physiograph and expression of HSP 70 was characterized by western blotting, respectively. Potassium chloride (55 mM) significantly augmented vascular contractility of yat aorta by 39% compared with the control at 8 hours but not one or three hours after treatment of 4 mM arsenic. Arsonic stress (4 mM) also increased the expression of HSP 70 in rat aorta at 8 hours but one or three hours compared with the control and HSP expressed in vascular smooth muscle cells and some expressed in endothelium cells. These results suggest that arsenic stress not only did alter the magnitude of the contractile response to high potassium chloride but also increased the expression of HSP 70 in the rat aorta.

Changes of Vascular Contraction and Relaxation of Rat aorta under Arsenic Stress (비소 스트레스에 의한 흰쥐 대동맥의 수축과 이완반응의 변화양상)

  • 권윤정;박태규;성유진;김인겸;김중영
    • Journal of Life Science
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    • v.13 no.5
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    • pp.634-641
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    • 2003
  • In order to examine whether arsenic, one of environmental stress, contribute to augumentation and relaxation of rat aorta, this study was performed in vivo and in vitro, using intacted or denuded rats aorta ring preparation, respectively. The carotid arterial pressure was recorded on an ink-writing physiograph(Grass Co. 79E) connected to strain gauge. The contractile response of vascular ring with or without endothelium preparation isolated from rat were determined in organ bath and was recorded on physiograph connected to isometric transducer. Vasopressin-,and phenylephrine- induced increase in arterial pressure significantly enhanced in arsenic-treated rats; increase of 19.1%, and 46.6%, respectively. Vascular contractile response was measured in vitro preparations exposed to 0, 0.5, 1, 2 and 4 mM of arsenic for 1, 3, 5 and 8 hours. The dose-vascular responses of phenylephrine augmented by increasing dose of arsenic in the strips exposed to arsenic for 8 hours, and did not augmented for 1, 3, 5 hours. The phenomenon was not affected by strips denuded endothelium. And the response of relaxation of rat aorta induced by nitroprusside was not influenced by arsenic stress, but acetylcholine was a little increased. compared to that of control. There were no significant difference in relaxation between control and arsenic treated rings with endothelium or denuded. All of the results, phenyleprine-induced vascular contraction was significantly enhanced in 4 mM arsenic-treated rat aortic rings compared with control, whether endothelium was present or denuded at 8 hours after arsenic treatment. It may be a mechanism by which long-term arsenic stresses play a role in development of hypertension.

뇌혈류 자가조절과 내인성 $K^{+}$ channel 개방물질에 대한 연구

  • 홍기완
    • Proceedings of the Korean Society of Applied Pharmacology
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    • 1993.04a
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    • pp.85-85
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    • 1993
  • 뇌동맥계는 일과성 저혈압에 반응하여 혈관확장이 야기되고, 혈압 상승시에는 혈관수축이 일어남으로서 뇌혈류가 일정하게 조절된다. 이러한 자가조절은 뇌손상 등의 병적 상태에서 야기된다. 연구의 목적은 \circled1 Cromakalim, CGRP(calcitonin-gene related peptide), 및 substance P에 의하여 뇌연막동맥의 직경이 어떻게 변동하는가를 관찰하고 \circled2 이들 신경성 peptide의 작용에 대하여 $K^{+}$ 통로 개방 봉쇄제인 glibenclamide의 전처치 효과를 검색하고 \circled3 Capsaicin 전처치가 뇌혈류 자가조절에 어떻게 영향을 미치는가를 검색하였다. 그 결과는 다음과 같다. 1. 뇌혈류 자가조절은 대퇴동맥을 통한 사혈에 의하여 혈압하강을 일으킬 때 뇌연막 동맥은 이완하였고, reservoir내의 혈액을 체내로 주입함로서 혈압반전을 일으켰을 때는 혈관 수축이 일어났다. 2. 연막동맥은 glibenclamide (1~3$\mu$M)의 관류에 의하여는 영향을 받아니하였다. 3. 혈압변동에 따른 혈관직경의 변화를 회기직선으로 분석하였다. Glibenclamide 1과 3$\mu$M의 전처치 관류에 의하여 혈압하강에 따른 혈관 이완경사도와 혈압반전에 따른 혈관수축 경사도가 대조군에 비하여 현저히 약화되었다. 4. Cromakalim (0.1-30$\mu$M)의 각 농도를 대뇌표면에 관류시 연막동맥의 기초직경은 약물농도에 의존하여 증가되었고, 이는 glibenclamide (1$\mu$M) 전처치 관류에 의하여 억제되었다. 5. CGRP (0.1~100 nM)와 substance P (0.1~10nM)도 용량에 의존하여 혈관이완을 일으켰다. 전자는 glibenclamide (1$\mu$M) 전처치 관류에 의하여 억제되었으나 후자는 영향을 받지 아니하였다. 6. Capsaicin(50 nmol: intracisternally) 주사에 의하여 뇌혈류자가조절의 변동이 초래되었다. 이상의 결과들을 종합하면 CGRP가 혈압변동에 의하여 반사적으로 유리되고, 이는 glibenclamide-sensitive $K^{+}$ 통로에 작용하는 것으로 시사된다.

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Reversible Cerebral Vasoconstriction Syndrome Presenting as Transient Vessel Wall Enhancement on Contrast-Enhanced Fluid-Attenuated Inversion Recovery Images: A Case Report and Literature Review (조영증강 유체감쇠반전회복기법 영상에서 일과성 혈관 벽 조영증강으로 나타나는 가역성 대뇌 혈관 수축 증후군: 증례 보고 및 문헌 고찰)

  • Sun Ah Heo;Eun Soo Kim;Yul Lee
    • Journal of the Korean Society of Radiology
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    • v.81 no.5
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    • pp.1239-1245
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    • 2020
  • Reversible cerebral vasoconstriction syndrome (RCVS) is a clinical and radiological syndrome with primary features that include hyperacute onset of severe headache and segmental vasoconstriction of the cerebral arteries, which resolve within 3 months. Vessel wall enhancement has been reported in some cases of RCVS; however, its pathophysiological and diagnostic implications remain unclear. We review a case of RCVS in a patient with transient vessel wall enhancement on contrast-enhanced fluid-attenuated inversion recovery images, focusing on the pathophysiological and diagnostic implications.

영상인식을 이용한 혈관조영기(Angiography)의 정량분석

  • Lee, Dong-Hyeok;Kim, Hui-Chan;Min, Byeong-Gu
    • Proceedings of the KOSOMBE Conference
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    • v.1994 no.05
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    • pp.19-22
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    • 1994
  • 심장과 혈관의 고해상도 영상을 얻어 심질환에 관한 정보를 얻는데는 혈관조영기(Angiograph)가 가장 유용하게 사용되고 있다. 본 연구는 혈관조영기의 정량분석을 위한 영상 알고리즘을 구현하였다. 심장의 수축 이완에 따른 심벽의 부위별 움직임과 심장 체적 변화를 측정 수치화하고 혈관을 따라가면서 혈관의 두께를 기록하는 프로그램을 작성하였다. 영상획득과정에서 생기는 잡음과 위치오차를 없애는 전처리를 거친 후에 구조적 형태 인식법(Structural Pattern Recognition)으로 인식 알고리즘을 구현하였다. 14장의 심장의 수축이완 연속사진과 2장의 관상동맥 혈관조영사진을 분석한 결과 비교적 정확한 측정을 해내는 것을 관찰할 수 있었다.

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The Convergence Effect of Phloretin Existent in Plants on Vascular Contractility (플로레틴(Phloretin)의 혈관내피수축 융합효과와 관련기전 연구)

  • Bang, Joon Seok;Je, Hyun Dong;Min, Young Sil
    • Journal of Convergence for Information Technology
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    • v.10 no.10
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    • pp.143-149
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    • 2020
  • This study tried to observe the ability to inhibit vasocontriction in phloretin - the primary ingredient of apple tree leaves and the Manchurian apricot - through ROCK(Rho-associdated, coiled-coil containing protein kinase) inactivation in rat aortae. A piece of artery that was separated from Sprague-Dawley male rats and retained or damaged the endothelium was suspended in myograph tank with two metal rings, the lower ring fixed to the bottom of the tank, and the upper ring connected to the isotonic force transducer. Interestingly, phloretin inhibited fluoride- or phorbol ester-provoked contraction implying that additional pathways dissimilar from endothelial nitric oxide synthesis such as ROCK or MEK (mitogen activated protein kinase kinase) inactivation might be involved in the vasorelaxation. Therefore, this study provides that phloretin participates in the reduction of ROCK or MEK activity in smooth muscle in addition to the endothelial-dependent action of the endotheliuim in complete blood vessels, and consequently inhibits actin-myosin interaction in smooth muscle. Furthermore, phloretin inhibited thromboxane A2-induced contraction suggesting the mechanism including inhibition of ROCK and MEK.

Effect of Quinolinedione Derivative on Blood Vessels and Its Acute Toxicity (Quinolinedione 유도체에 의한 혈과 수축작용 및 급성독성 연구)

  • 이선구;배옥남;강규태;이주영;유충규;김화정;정진호
    • Journal of Food Hygiene and Safety
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    • v.14 no.3
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    • pp.282-286
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    • 1999
  • OQ-21을 암·수 ICR계 마우스에 복강투여 하여 급성독성을 측정한 결과 최대용량 투여군에서도 사망한 동물은 관찰되지 않았다. 그리고 시험동물을 부검하여 육안 관찰한 결과 OQ-21 투여군은 대조군과 전혀 차이가 없었고 실제 독성도 비교적 낮은 것으로 판단된다. 또한 OQ-21이 혈과에 수축 반응에 영향을 미치는 지를 연구한 결과 용량 의존적으로 phenylephirne에 의한 혈관 수축을 증가시킴을 관찰하였다. 이상의 결과로부터 OQ-21은 급성독성이 약한 것으로 생각되지만 혈관 수축에 미치는 영향은 앞으로 인체 안전성에 관하여 검토하여야 할 과제로 사료된다.

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Convergence Study of Cell Viability and Vascular Relaxtion of Hanbang-tea Prescrpition (한방차 조성물의 세포활성과 혈관이완 효과에 대한 융합적 연구)

  • Park, Sung-Hye;Min, Je-Ho
    • Journal of the Korea Convergence Society
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    • v.8 no.2
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    • pp.291-297
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    • 2017
  • This study was aimed to secure the basis for developing the hangbang-tea may help promote healthy blood vessels by natural herbal ingredients formulated in accordance with the basic principles of oriental medicinal theory. We investigated the vessels contracted by concentrations and safety assessment carried out by the cell viability of Taraxaci Herba, Gardeniae Fructus, Chrysanthemum indicum and Lonicerae Flos composition and concentration. We found cell survival were higher than the control group show a beneficial trend in the growth of normal liver and kidney cells. As a results of this study will be the basis to develop the hangbang-tea differentiated in the future oriental medicine resources. Medicinal resources will be hangbang-tea based on clinical trials utilizing herbal western and oriental medicine convergence principle and vascular relaxation mechanism.

The characteristics of cholinergic responses in tilapia dorsal aorta (틸라피아 배대동맥의 콜린성 반응의 특성)

  • Choi, Dong-Lim;Chung, Joon-Ki
    • Journal of fish pathology
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    • v.9 no.1
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    • pp.53-63
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    • 1996
  • The present study was undertaken to investigate the physiological characteristics of the cholinergic responses in the tilapia dorsal aorta. In vessels under resting tension or precontracted with norepinephrine, acetylcholine caused only concentration-dependent vasoconstrictions. Contractile response to acetylcholine was not affected by the removal of endothelium or the application of methylene blue. Atropine, gallamine or pirenzepine shifted concentration-response curve to the right. However pirenzepine showed a similar effect on the curve only at high concentration ($1{\times}10^{-5}$M). Acetylcholine-induced vasoconstriction was not markedly influenced by indomethacin, or verapamil, but was almost abolished in the calcium-free physiological buffer solution. These results suggest that acetylcholine produces only an endothelium-independent vasoconstriction in tilapia dorsal aorta and that the contractile effect of acetylcholine is mainly mediated by the activation of $M_2$ subtype receptor, which might be associated with the extracellular calcium influx through receptor-linked calcium channel.

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