• Title/Summary/Keyword: cocaine

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Cortisone 및 Calcium이 국소마취약의 Acetylcholine 근련축억제효과에 미치는 영향

  • Baei, Yu-Hong;Hahm, Jhong-Dai;Lee, Sang-Sin
    • The Journal of the Korean dental association
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    • v.12 no.6
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    • pp.419-423
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    • 1974
  • The authors have investigated the roles of cortisone and calcium on the depressive effects of local anesthetics on the acetylcholine-induced skeletal muscle contraction in frog. The results are as follows. 1. Tetracaine, cocaine, lidocaine and procaine decreased the acetylcholine-induced skeletal muscle contraction. 2. Cortisone increased the depressive effects of local anesthetics on the acetyl-choline-induced skeletal muscle contraction. 3. There was a tendency that in high calcium concentration, the depressive effects of cocaine and lidocaine on acetylcholine-induced skeletal muscle contraction were increased.

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Neurobehavioral Teratology of cocaine (코카인의 신경행동 기형독성)

  • 김동구
    • Proceedings of the Korean Society of Applied Pharmacology
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    • 1993.11a
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    • pp.13-16
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    • 1993
  • 코카인은 열대지방에 광범위하게 분포되어 있는 Erythroxylon나무의 잎에 존재하고 있는 알칼로이드이다. 1536년 Pizarro가 스페인 침공을 마친 후 귀국하면서 유럽에 소개되었으며 Alfred Niemann에 의해서 1853년 처음으로 코카잎에서 추출되었고 "cocaine"이라고 명명되었다. 코카인은 황홀감을 일으킬 뿐 아니라 감기, 피부병, 천식, 류마치즘, 후두염 및 치통에도 효과가 좋다고 알려졌었고 국소마취효능이 좋아 아직까지도 안과 영역에서 가끔 사용되고 있다. 그러나 코카인은 인류가 알고 있는 물질중 가장 강화(reinforcement)효과가 강한 물질이기에 현재 법적으로 그 사용이 국소마취제 이외에는 금지되어 있으나 황홀감을 얻기위한 불법적인 사용이 크게 늘어있는 형편이다.늘어있는 형편이다.

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Review on some diseases which are differentiated with AMI (심근경색과 감별할 주요질환)

  • Kim, Jeong-A
    • The Journal of the Korean life insurance medical association
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    • v.31 no.1
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    • pp.10-14
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    • 2012
  • The importance of the diseases which are differentiated with acute myocardial infarction (AMI) cannot be overemphasized in insurance medicine. Although there are lots of diseases similar with AMI, in this paper, 5 diseases were described; Myocardial bridging, cocaine toxicity, myocarditis, cardiac syndrome X, and Takotsubo syndrome. Costs of the interventions like coronary angiography or echocardiography are relatively low in Korea compared to western countries. Therefore, detection of those diseases has been increased recently and illegal drug addiction also has been increased probably due to globalization. In conclusion, the knowledge of those diseases dealt with this article could be helpful for the person who is related to insurance medicine.

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Effects of Panax Ginseng on the Central Nervous System (인삼(人蔘)의 중추신경계(中樞神經系)에 대(對)한 작용(作用))

  • Oh, Jin-Sup;Park, Chan-Woong;Moon, Dong-Yeon
    • The Korean Journal of Pharmacology
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    • v.5 no.1
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    • pp.23-28
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    • 1969
  • Saponin, essential oil and fat oil fractions were fractionated from Panax Ginseng and their potentiating or inhibiting actions during the combined use of several central nervous system stimulants or depressants were observed to elucidate the possible role of Ginseng fractions on the central nervous system. Saponin, essential oil and fat oil fractions shortened nembutal sleeping time at low dosage (10 mg/kg) but contrarily they produced potentiation of nembutal hypnosis at high dosage (50mg/kg). In the toxicity study of amphetamine, saponin and essential oil fractions reduced the toxicity in aggregated mice at high dosage (100 mg/kg) but such decreased lethality was not observed in isolated mice. Ginseng fractions, especially high dose of saponin fraction (100mg/kg) prolonged the survival time after injection of convulsive dose of metrazol or cocaine and saponin fraction also prolonged the onset of cocaine convulsion at high dosage (100 mg/kg).

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Production of Monoclonal Antibody against the Principal Metabolite of Cocaine, Benzoylecgonine (코카인의 주대사물인 벤조일에코닌에 대한 단일클론 항체의 제작)

  • Nam, Kyung-Soo;Kim, Jae-Wha;Oh, Eun-Suk;Choi, Myung-Ja;Choi, In-Seong;Chung, Tai-Wha
    • YAKHAK HOEJI
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    • v.36 no.2
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    • pp.188-190
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    • 1992
  • Two clones of monconal antibodies(Co-1 and Co-2) against BSA-benzoylecgonine(BSABE) were produced. Both monoclonal antibodies showed high binding affinity to BSA-BE. Observing from ELISA inhibition assay, Co-1 reacted only weakly with soluble benzoylecgonine, while Co-2 showed considerable reactivity with soluble benzoylecgonine.

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Pharmacological characteristics of higenamine on adrenergic β-receptors (아드레날린성 β-수용체에 대한 higemamine의 약리학적 특성)

  • Yun, Hyo-in;Chang, Ki-churl;Lee, Chang-eop
    • Korean Journal of Veterinary Research
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    • v.32 no.1
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    • pp.41-49
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    • 1992
  • Higenamine is an Aconiti tuber derived compound whose chemical structure is 1-(4'-hydroxybenzyl)-6, 7-dihydroxy-1, 2, 3, 4-tetrahydroisoquinoline containing catechol ring and tetrahydroisoquinoline nucleus in its own structure, both of which are well known to have agonistic effects on adrenergic receptors. Using guinea-pig atria(rich in ${\beta}_1$-receptor) and treachea(rich in ${\beta}_2$-receptor), we studied pharmacological actions of higenamine on these organs with special interest of its relevancy of ${\beta}$-receptor selectivity. In order to further clarify its pharmacological characteristics, the influncences of pretreatment of reserpine or cocaine were also investigated. The results were summarized as follows : 1. Higenamine had remarkable chronotropic, inotropic and bronchodilator effects in guinea-pig spontaneously beating right atria, left atria and trachea, in dose-dependent manners. 2. All of above actions were blocked competitively by propranolol, which shows nonselectivity of higenamine on ${\beta}$-receptor. $pA_2$ values of propranolol against higenamine were 7.93, 7.76 and 8.46 in guinea-pig right atria, left atria and treachea, respectively. 3. Reserpine pretreatment(5mg/kg, ip, 24h) did not show my decrease in pharmacological actions of higenamine, which suggests higenamine has direct action on ${\beta}$-receptor not via catecholamine release. 4. Cocaine pretreatment$(1{\mu}M)$ had no influence on pharmacological actions of higenamine in contrast with nor epinephrine, which suggests there is no neuronal uptake mechanism of higenamine in the studied organ preparations.

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Acupuncture Attenuates Cocaine-induced Dopamine Release in the Nucleus Accumbens and Voluntary Cocaine Intake in Rats (침자극이 코카인 투여로 인한 측핵내 도파민 유리와 자발적 코카인 섭취량에 미치는 효과)

  • Lee, Hak-in;Kim, Mi-ryeo;Kim, So-young;Shim, In-sop;Han, Sang-won;Jin, Chang-bae;Yang, Chae-ha
    • Journal of Acupuncture Research
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    • v.20 no.4
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    • pp.170-179
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    • 2003
  • 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.

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