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이종임,진창배,류재하,조정숙,Lee, Jong-Im,Jin, Chang-Bae,Ryu, Jae-Ha,Cho, Jung-Sook 대한약학회 2008 약학회지 Vol.52 No.2
The leaves of Perilla frutescens Britt. var. japonica Hara (Labiatae) are often used in gourmet food in several Asian countries. Two kinds of perilla cultivars, Namcheon (NC) and Bora (BR), have been respectively developed in Korea by the pure line of 'deulkkae' from the local variety and by the cross of 'deulkkae' and 'chajogi'. The present study evaluated and compared antioxidant and neuroprotective effects of the fractions prepared from the leaves of the two cultivars using cell-free bioassay systems and primary cultured rat cortical cells. We found that the spirit, chloroform, hexane and butanol fractions from NC and BR leaves inhibited lipid peroxidation initiated in rat brain homogenates by $Fe^{2+}$ and L-ascorbic acid. In contrast, only the spirit and butanol fractions from both cultivars exhibited 1,1-diphenyl-2-picrylhydrazyl radical scavenging activity. Among the fractions tested, the butanol fractions from NC and BR leaves exhibited the most potent antioxidant properties, and the butanol fraction from BR was more potent than the NC fraction. In consistence with these findings, the butanol fractions from both cultivars protected primary cultured cortical cells from the oxidative damage induced by $H_2O_2$ or xanthine and xanthine oxidase, with the BR butanol fraction being more active. The butanol fractions from NC and BR did not produce cytotoxicity in our cultures treated for 24 h at the concentrations of up to $100\;{\mu}g/ml$. Taken together, these results indicate that the leaves of the two cultivars of Perilla frutescens exert antioxidant and neuroprotective effects, and that the butanol fraction from BR leaves exhibits the most potent antioxidative neuroprotection among the fractions tested in this study.
이학인,김미려,김소영,심인섭,한상원,진창배,양재하,Lee, Hak-in,Kim, Mi-ryeo,Kim, So-young,Shim, In-sop,Han, Sang-won,Jin, Chang-bae,Yang, Chae-ha The Korean Acupuncture Moxibustion Medicine Societ 2003 대한침구의학회지 Vol.20 No.4
목적 : 침(鍼)은 정신이상 및 약물중독과 같은 많은 기능상의 장애질환을 치료, 조정하는데 널리 쓰이고 있으며, 중추신경계에서 생화학적인 균형을 유지하는데 기여한다고 밝혀져 있다. 동물 연구에서 코카인의 강화 및 민감화 특성과 중추의 도파민 활성과의 관련 가능성이 높아지고 있다. 본 연구에서는 약물중독 치료에 이용할 수 있는 침의 효과를 규명하기 위하여 침자극 후 급성 코카인 투여에 의한 도파민 유리 및 자발적 코카인 섭취량에 미치는 침자극의 효과를 측정하였다. 방법 : 웅성 SD 쥐에 코카인 (1mg/kg, i.v.)의 주사 직전 양측의 신문혈(HT7)을 1분간 침자극 한 후, 측핵내 세포외액의 도파민 및 대사산물의 함량변화를 미세투석법을 이용하여 HPLC로 분석하였다. 침자극 후 two-bottle, free choice protocol을 이용하여 자발적 코카인 섭취량의 변화를 관찰하였다. 별도의 쥐를 이용하여 1회 동량의 코카인 정맥주사하고 2주간의 철회를 거친 다음 two-bottle, free choice protocol을 실시하여 자발적 코카인 섭취량과 급성 코카인 투여 후 측핵 중 도파민유리증가율 사이의 상관관계를 조사하였다. 결과 : 신문혈(HT7) 자침이 코카인 1회 주사 후에 유도된 도파민 증가를 대조혈(내관혈(PC6), 또는 꼬리)에 비해 유의하게 억제하였으며 two-bottle choice protocol에 의한 동물의 자발적 코카인 섭취량을 억제하였다. 아울러 자발적 코카인 섭취량과 급성 코카인 투여 후 측핵 중 도파민유리증가율 사이에는 상관관계가 있었다. 결론 : 본 실험결과 침자극에 의해 자발적 코카인 섭취량이 억제되는 것은 측핵에서의 도파민 유리억제에 의해 중개되는 것으로 보여지므로 침자극은 코카인중독과 같은 약물의 중독치료에 이용될 수 있을 것으로 사료된다.
Angiotensin 변환 효소 억제제인 Captopril 유도체들의 구조와 활성관계 연구 수용액상의 분자동력학적 연구의 중요성
박종세(Jong Sei Park),지명환(Myung Whan Chi),윤창노(Chang No Yoon),진창배(Chang Bae Jin) 한국응용약물학회 1994 Biomolecules & Therapeutics(구 응용약물학회지) Vol.2 No.1
In order to investigate the structure-activity relationships of the stereoisomers of angiotensin converting enzyme inhibitors, captopril and its derivatives were selected as model compounds. In vitro enzymatic activities of them depend on the symmetry at the asymmetric carbons. Especially, the alanyl carbon should have the S configuration to be biologically active. But the demethylated captopril having the achiral carbon also shows the activity although it is less active than captopril. Seven stereoisomers of captopril and its derivatives were chosen and their acidic and ionic forms were used for molecular dynamics simulations. Four computer simulations were practiced for each model compound in order to obtain the good condition for simulation to explain the experimental structure-activity relationships. From the computer simulation results, relativistic movements of three well-known pharmacophoric sites, carboxylate carbon, carbonyl oxygen, and sulfur atoms, were analyzed. Good results were obtained from the aqueous solution molecular dynamics simulation with ionic forms of model compounds. Active model compounds have the pharmacophoric areas of 6.08 to 6.38 Ų and the similarity in the geometrical data. But inactive ones have the largely deviated values of 4.51 to 4.87Ų from those of active ones.
신규 백금착물 항암제 KBP31705-C127 , KBP30603-901 의 Clsplatn 및 Carboplatin 과의 약동력학적 동태 비교
정인숙(In Sook Jung),이주선(Ju Seon Lee),허수정(Soo Jung Huh),김진숙(Jin Sook Kim),진창배(Chang Bae Jin),김동현(Dong Hyun KIm),김명수(Myung Soo Kim),박경수(Kyung Su Park),손연수(Youn Soo Sohn),백형기(Hyoung Gee Back),조양하(Yang Ha C 한국응용약물학회 1996 Biomolecules & Therapeutics(구 응용약물학회지) Vol.4 No.4
The present study examined pharmacokinetic profiles of KBP31705-C127 and KBP30603-901, new platinum coordination complexes synthesized as anticancer candidates, in comparison with two well-known platinum-containing anticancer agents, cisplatin and carboplatin in rats. Under sodium pentobarbital anesthesia of male Sprague-Dawley rats, urinary bladder, and femoral artery and vein were catheterized for urine collection, blood sampling and drug injection, respectively. Following i.v, administration of cisplatin (2 ㎎/㎏), KBP31705-C127 (2 ㎎/㎏), carboplatin (20 ㎎/㎏) or KBP30603-901 (20 ㎎/㎏), blood samples were collected at 2, 4, 6, 8, 10, 15, 20, 30, 45, 60 and 120 minutes. Urine samples were collected at 1-hr interval for 4 hr. Platinum concentrations in plasma and urine were measured using an inductively coupled plasmamass spectrometer. The plasma concentration-time curves were biphasic for all drugs during the time period studied. Compared with cisplatin, KBP31705-C127 showed similar decay patterns in the alpha- and beta-phases with slightly lower plasma concentrations. Urinary platinum excretion for cisplatin and KBP31705-C 127 was 56 and 52% of the administered dose in 4 hr, respectively. With regard to carboplatin and KBP30603-901, a similar decay pattern was also observed in the alpha-phase. The half life of KBP30603-901 in the beta-phase, however, was much longer than that of carboplatin, which was consistent with the urinary excretion results that 46 and 59% of the administered dose were excreted in the urine in 4hr, respectively. The results suggest that platinum coordination complexes are primarily excreted via the renal route and KBP30603-901 can elicit longer duration of action due to slower renal excretion compared to carboplatin.
김낙두(Nak Doo Kim),한병훈(Byung Hoon Hahn),이은방(Eun Bang Lee),공재양(Jae Yang Kong),김명혜(Myoung Hae Kim),진창배(Chang Bae Jin) 한국생약학회 1979 생약학회지 Vol.10 No.2
Two pure saponin components, Panax saponin C (protopanaxatriol derivative, ginsenoside Re) and Panax saponin E (protopanaxadiol derivative, ginsenoside Rb_l) were isolated from Panax ginseng root and their acute toxicities in mice and antistress effects in rats were investigated. Average lethal doses (LD_(50)) of ginsenoside Re were 130㎎/㎏ (i.v.), more than 1,000㎎/㎏ (i.p.) and more than 1,500 ㎎/㎏ (s.c.), respectively. Average lethal dose of ginsenoside Rb₁ was 243㎎/㎏ intravenously. Adrenal ascorbic acid and cholesterol contents were significantly decreased when normal rats were exposed to heat (40℃) for 30 min. The reduction of the adrenal ascorbic acid and cholesterol contents in rats was partially prevented when the rats received the ginseng saponins prior to exposure to heat stress and most pronounced effects were observed in rats received ginsenoside Re. However, it was found that administration of ginseng alone, without stress, did not significantly change the ascorbic acid and cholesterol contents in adrenal glands. Eosinophil counts in the blood of the rats were elevated when the rats were exposed to the heat stress, and the elevation of the eosinophil counts were prevented with the ginseng saponins under the stress, but the changes were all insignificant statistically.
김진안,조효제,진창배 부산대학교 1994 生産技術硏究所論文集 Vol.47 No.
It is an important problem to consider the mechanism of capsizing of a ship in waves in the design of ship. Especially, the inclined vessels which were caused by the cargo shift or inclining initially by the wind force etc, are easy to be capsized in comparison with the upright vessel. In this paper, we investigate the characteristics of roll motion of the inclined vessel in following seas by meas of the analysis of parametric oscillation. We derived the nonlinear equation of motion to express the roll motion of the inclined vessel and compared with behaviour of the upright vessel. It is known that capsizing phenomena of the inclined vessel which occur instantaneously in the following seas, can be explained well by the solution of the nonlinear equation. 파랑중 선박의 전복 메카니즘을 규명하는 것은 선박의 안전한 설계를 위하여 다루어져야 할 또하나의 중요한 문제이다. 특히 적하물의 이동이나 바람에 의한 경사모멘트 등에 의하여 경사된 선박의 경우에는 직립선에 비하여 전복될 위험이 많은 것으로 알려져 있다. 따라서, 본 논문에서는 파라메트릭 진동의 관점에서 추파중을 항해하는 초기 경사선의 횡요운동 특성을 조사하여, 선체의 전복 현상을 고찰한다. 위를 위하여 우선 초기 경사선에 대한 비선형 운동방정식을 유도하여 그 운동방정식의 해를 직립선에 대한 것과 서로 비교 검토하였다. 그 결과 추파중을 항해하는 초기경사선이 아주 짧은 시간에 전복하는 현상은 본 논문에서 설정한 비선형 운동방정식으로서 충분히 설명할 수 있음을 보였다.