• Journal of Pharmaceutical Investigation
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• 제15권1호
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• pp.22-31
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• 1985

The influence of some sympathetic blocking agents on pressor actions of norepinephrine and angiotensin was investigated in rabbits. 1. Phentolamine, sympathetic ${\alpha}-blocking$ agent, blocked the pressor action of norepinephrine, but did not affect the pressor action of angiotensin 2. Chlorisondamine, autonomic ganglionic blocking agent, potentiated the both actions of norepinephrine and angiotensin. 3. Guanethidine, bethanidine and debrisoquine, sympathetic neuronal blocking agents, potentiated the action of norepinephrine, while diminished that of angiotensin. 4. Reserpine, norepinephrine depleting agent, increased the pressor response of norepinephrine, but did not influence the pressor action of angiotensin.

• 생명과학회지
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• 제12권5호
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• pp.549-554
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• 2002

포공영약침액의 암억제 효과를 살펴보기 위하여 quinone reductase (QR) 생성유도를 생쥐의 간암세포인 Hepa Iclc7를 이용하여 측정한 결과, 포공영약침액을 처리한 Hepa Iclc7에서 QR생성이 유도되었다. 또한 포공영약침액은 phase II detoxification 효소인 glutathione S-transfer-ase (CST) 활성을 증가시키고 glutathione 생성도 증가시켰다 QR과 CST는 간세포에서 주로 생성되는 phase II효소로 발암물질에 의해 일어나는 돌연변이와 종양화 효과를 막아주고 발암물질을 무독화 시키는 것으로 알려져 있다. 따라서 본 실험에서 포공영약침액은 QR 효소 생성 유도, glutathione 함량 증가 및 CST 효소활성 증대등 phase II detoxification의 기작을 통한 발암과정의 blocking agent로서 효과가 있음을 알 수 있었다.

• 한국멀티미디어학회논문지
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• 제14권1호
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• pp.144-152
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• 2011

IPv4 주소가 고갈되어가고 있기 때문에 IPv6 주소의 사용이 늘어나고 있다. IPv6 환경에서는 주소자동설정 기능이 제공된다. 주소가 각 호스트(host)에 자동으로 할당될 경우, 네트워크 관리 시스템은 모든 장비의 IP주소를 조사하고 해당 정보를 유지해야 하는 어려움이 따른다. 또한, IP주소가 자동으로 설정되기 때문에 악의적 사용자가 아무런 제약 없이 네트워크 주요장비에 접근할 수 있는 문제가 발생한다. 이런 문제를 해결하기 위해 악의적 사용자들에 대한 관리 및 차단이 필요하다. 본 논문에서는, IPv6 환경에서 호스트를 탐색하고 인가되지 않은 호스트가 네트워크에 접속하는 것을 차단함으로써, 네트워크 주요 자원을 효율적으로 관리하고 보호하는 호스트 탐색 및 네트워크 접속 차단 에이전트 시스템을 제안한다. IPv6 환경에서 본 에이전트 시스템의 성능을 테스트한 결과, 본 시스템은 정상적으로 탐색과 차단 기능을 수행하였다.

• 약학회지
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• 제30권3호
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• pp.111-120
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• 1986

The influence of debrisoquine on pressor actions of norepinephrine (NE) and tyramine (TR) was investigated in rabbits. Debrisquine(D), in the doses of 1.0, 3.0 and 6.0.mu.g/kg, i.v. potentiated significantly the pressor actions of NE and TR, except the action of TR in the dose of 1.0mg/kg of debrisoquine. NE response potentiated by debrisoquine was not affected by tranylcypromine, a MAO inhabiter, or desipramine, a NE uptake blocking agent, but augmented by reserpine, a NE depleting agent, or bethanidine, a sympathetic neuronal blocking agent. NE response potentiated by tranylcypromine or desipramine was augmented by debrisoquine, while NE response potentiated by reserine or bethanidine was not affected by debrisoquine. TR response potentiated by debrisoquine was weakened by tranylcypromine, desipramine or reserpine, and not affected by bethanidine. TR response in rabbit pretreated with tranylcypromine, desipramine or reserpine was augmented by debrisoquine, but in rabbit pretreated with bethanidine was not affected by debrisoquine.

• Macromolecular Research
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• 제13권5호
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• pp.427-434
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• 2005

To improve the performance and reduce raw material costs, blocked isocyanates were prepared with mixture of blocking agents in many industries. Three blocked isocyanates (adducts) namely $\varepsilon$-caprolactam/benzotriazole-blocked 4,4'-diphenylmethane diisocyanate (MDI), toluene-2,4-diisocyanate (TDI) and 4,4'-dicyclohexyl-methane diisocyanate ($H_{12}$MDI) were synthesized. Six reference adducts were also prepared by blocking MDI, TDI, and $H_{12}$MDI with $\varepsilon$-caprolactam ($\varepsilon$-CL) or benzotriazole. The reactions were carried out in acetone medium and dibutyltin dilaurate (DBTDL) was used as a catalyst. The progress of the blocking reaction was monitored by IR spectroscopy. De-blocking temperatures (dissociation temperatures) of these adducts were studied using DSC and TGA and the results were correlated. As expected, the thermal analysis data showed that de-blocking temperature of blocked aromatic isocyanates was lower than that of the blocked aliphatic isocyanates. The low de-blocking temperature of blocked aromatic isocyanate could be due to electron withdrawing benzene ring present in the blocked isocyanates. It was also found that benzotriazole-blocked adducts de-blocked at higher temperature compared with $\varepsilon$-CL-blocked adducts.

• Elastomers and Composites
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• 제40권4호
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• pp.249-257
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• 2005

폴리우레탄 프리폴리머들이 폴리올과 디이소시아네이트로부터 제조되었다. 이온화되지 않은 폴리우레탄 프리폴리머들은 폴리프로필렌 글리콜(PPG, MW:1000), 디메치롤 프로피온산(DMPA)과 이소포론 디이소시아네이트(IPDI)를 사용하여 합성되었다. 폴리올과 디이소시아네이트의 몰비를 변화시키면서 합성된 폴리우레탄 프리폴리머들은 물에 분산된 후 물성을 측정하였다. 실험결과는 프리폴리머가 하드세그먼트 40%, NCO 3.43%, [NCO]:[OH]=1.5:1.0의 조건에서 가장 안정한 분산액을 보여 주었고, 30%의 고형분으로 물에 분산되었다. 폴리우레탄 프리폴리머들은 또한 PPG와 DMPA의 몰비를 변화시키면서 합성되었다. DMPA의 몰비가 높을 때 폴리우레탄 수분산액의 입경은 감소하였다 3가지 종류의 말단기 차단제(blocking agent)를 사용하여 제조된 폴리우레탄 프리폴리머들은 사용된 차단제에 따라 각각 다른 초기 해리 온도를 나타내었고 3가지 종류의 차단제에 대한 해리의 시작은 모두 30분 안에 일어났다.

• 약학회지
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• 제22권3호
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• pp.138-147
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• 1978

Bethanidine, which is known as a sympathetic blocking agent, was injected into the vein of a dog in an attempt to investigate the influence on renal funciton. Bethanidine resulted in an increased urine flow and glomerular filtration rate, and it produced an increase of urinary sodium and potassium excretion and a decrease of reabsorption rate of sodium and potassium in renal tubules, whereas renal plasma flow showed no significant changes. After pretreatment of phentolamine, a specific alpha adrenergic blocking agent, bethanidine did not significantly increase glomerular filtration rate and diuresis, significantly increased urinary sodium and potassium excretion although the magnitudes were reduced when compared with that of bethanidine alone. In conclusion, bethanidine-induced diuresis appears to be the result of an inhibited tubuler reabsorpting of electrolytes within the kidney through its sympathetic blockade of renal nerves and of an increased glomerular filtration rate, which was caused by the constriction of vas efferense in the glomeruli.

• 약학회지
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• 제36권4호
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• pp.379-389
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• 1992

In order to investigate the effect of nifedipine, $Ca^{+2}$ channel antagoninst, on the action of some drugs participating in blood pressure, this experiment was peformed in rabbits. Nifedipine decreased the pressor actions of norepinephrine, angiotensin and carotid artery clamping, but did not affect the pressor actions of tyramine and depressor actions of acetylcholine and pilocarpine. Nifedipine inhibited the potentiated pressor action of norepinephrine and angiotensin, but did not influence the potentiated pressor action of tyramine in rabbits pretreated with chlorisondamine, ganglionic blocking agent. Nifedipine weakened the potentiated pressor action of norepinephrine, did not affect the pressor action of angiotensin and the potentiated pressor action of tyramine in rabbits pretreated with debrisoquine, sympathetic neuronal blocking agent.

• Archives of Pharmacal Research
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• 제13권2호
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• pp.136-141
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• 1990

The vasorelaxant effects of KR-30075 in guinea-pig pulmonary, bovine coronary and renal arterial strips contracted by either$K^+$depolarization, phenylephrine, or prostaglandin $F_{2a}$($PGF_{2a}$) were evaluated. KR-30075 was more potent than imazodan as a vasorelaxant against $PGF_{2a}$-induced contractions in bovine coronary and renal arteries, whereas against$K^+$induced contractions KR-30075 was less potent than imazodan in guieapig pulmonary arteries and more potent in bovine coronary arteries. KR-30075 was more potent against contractions induced by phenylephrine or $PGF_{2a}$ than the contractions induced by $K^+$ This profile of activity for KR-30075 was similar to that of imazodan and dissimilar from the calcium entry blocking agent nifedipine. There was no vascular selectivity of KR-30075 between bovine coronary and renal arterial strip preparations. In conclusion, this study shows that KR-30075 represents the vasorelaxant effects on guinea-pig pulmonary, bovine coronary and renal arteries without specific vascular selectivity. The vasorelaxant profile of KR-30075, with different sources of vascular smooth muscle, is unlike that of calcium entry blocking agent and more similar to the profile of the agent that inhibit cyclic nucleotide phosphodiesterase.

• Clinical and Experimental Pediatrics
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• 제46권2호
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• pp.192-194
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• 2003

가정분만으로 태어난 후 생후 6일된 신생아에서 전신성 강직-간대 경련이 발생하여 내원한 환아에서, 병력과 진찰 소견상 신생아 파상풍으로 진단하여 근이완제 및 인공환기요법으로 치료한 1례를 경험하였기에 보고하는 바이다.