• 한국식품영양과학회지
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• 제35권2호
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• pp.132-138
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• 2006

혈전성 질환을 예방 및 치료할 수 있는 트롬빈 직접 저해제 개발은 전 세계적으로 지속적으로 이루어지고 있다. 본 연구에서는 안전성이 확보된 식용 및 약용식물로부터 트롬빈 직접저해제를 탐색하였으며, 그 결과 메밀 종자의 메탄올 추출물 및 주정 추출물에서 강력한 트롬빈 저해활성을 확인하였다. 메탄올 추출물의 순차적 유기 용매 분획 결과 부탄올 및 에틸아세테이트 분획물에서 가장 우수한 트롬빈 저해활성을 나타내었다. 특히 주정 추출물의 부탄올 분획의 경우 $312.5{\mu}g/mL$의 낮은 농도에서도 $2,000\%$이상의 트롬빈 저해 활성을 나타내어, 아스피린보다 매우 효율적으로 혈전 생성을 억제함을 확인하였다. 활성성분은 30 KD 이상의 고분자 비단백질 성분임을 확인하였으며, 산 및 열처리에 의해 급격한 활성 감소가 나타나, 활성 물질의 효율적인 이용을 위해서는 메밀 종자의 비열, 비산 처리공정이 필요하리라 추측되었다. 또한 활성 분획물은 ICR 마우스를 이용한 폐색전 실험, 전뇌 허혈성 실험 및 치사유발실험에서 아스피린보다 우수한 혈전성 마비 억제, 혼수방지 및 치사억제 활성을 보여, 혈행 개선제 및 항혈전제로 개발 가능함을 제시하였다.

• 동의생리병리학회지
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• 제16권2호
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• pp.245-256
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• 2002

This studt was investigated to prove the effect of SPBST on the hypertension, the thrombosis and the brain damage. The results were as follows; 1. SPBST affected the htpertension as adepressant, but insignificant. 2. SPBST decreased significantly dopamine, aldosterone but ineffective on the epinephrine, norepinephrine and renin activity. 3. SPBST increased the NO product but insignificant. 4. SPBST had a death suppression effect by 50% in pulmonary thrombosis inducement experiment and activated slightly on the fibrinolytic activity. 5. SPBST suppressed significantly platelet diminution and prolonged insignificantly PT and APTT. 6. On the measure of the blood flow rate induced by the thrombus, in vivo SPBST accelerated the blood flow rate, in vitro insignificant. 7. SPBST had no toxicity on the PC12 cell and B103 cell induced by amyloid β protein (-35) and a protective effect, in proportion to the density. 8. SPBST decreased significantly coma duration time in a Infatal dose of KCN and showed 50% of survival rate in a fatal dose. 9. SPBST decreased significantly ischemic area and edema incited by the MCA blood flow block. These results indicate that SPBST can be used in hypertension, the thrombosis, the brain damage, the ischemic cerebral infarction and the acute stage of the brain damage. Further study will be needed about the functional mechanism and etc.

• 동의생리병리학회지
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• 제17권3호
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• pp.728-737
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• 2003

This study was investigated to prove the effect of GMGHT on the gultamate receptor, free radical and brain damage in rats sujected to Brain Ischemia The results were as follows; 1, GMGHT showed significant inhibitory effect of GMGHT on LDH release induced by NMDA, AMPA, and kinate. 2. GMGHT showed significant inhibitory effect of GMGHT on LDH release induced by BSO and Fe/sup 2+/. 3. GMGHT decreased coma duration time in a infatal dose of KCN and showed 30% of survival rate in a fatal dose. 4. GMGHT decreased ischemic area and edema incited by the MCA blood flow block. 5. GMGHT showed improvement of forelimb and hindlimb test after MCA occulusion in neurological exemination. 6. GMGHT showed no significant change after MCA occulusion in pathological observation as normal group. These results indicate that GMGHT can be used in the brain damage sujected to Brain Ischemia. Further study will be needed about the functional mechanism and etc.

• 대한한의학회지
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• 제25권3호
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• pp.32-44
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• 2004

Objectives : This study was undertaken to prove the effect of GSHT on the glutamate receptor, free radical and brain damage in rats subjected to brain ischemia Methods : Levels of cultured cortical neuron death caused by toxic chemicals were measured by LDH release assay. Neuroprotective effects of GSHT on brain tissues were examined in vivo by ischemic model of middle cerebral artery (MCA) occlusion. Results : GSHT showed significant inhibitory effect on LDH release induced by NMDA-kinate-Fe/sup 2+/. GSHT remarkably decreased coma duration time in a nonfatal dose of KCN and showed higher survival rate in a fatal dose. GSHT remarkably decreased ischemic area and edema induced by the MCA blood flow block. GSHT showed high improvement of forelimb and hind limb test after MCA occlusion in neurological examination. GSHT showed no significant change after MCA occlusion in pathological observation of the normal group. Conclusions : These results indicate that GSHT can be used to treat the brain damage caused by brain ischemia. Further study will be needed about the functional mechanism, etc.