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  • 우리나라 백부자의 적출 조개 심장운동에 대한 작용
  • The Action of Extract of Aconitum koreanum R. Raymond on Isolated Clam Heart
저자명
하병국(Ha, Byoung-Kuk),김유성(Kim, Yoo-Sung),김원자(Kim, Won-Ja),박철훈(Park, Chul-Hoon),
간행물명
대한약리학잡지
권/호정보
1972년|8권 1호(통권10호)|pp.15-26 (12 pages)
발행정보
대한약리학회|한국
파일정보
정기간행물|KOR|
PDF텍스트(0.58MB)
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영문초록

Korean aconitum (Aconitum koreanum R. Raymond) as one of the botanical crude drugs which pertain to helleboraceae has been extensively applied in Chinese medicine during the past decades. It has been particularly used in immortal tonic among the folk remedies in China, however, its general uses comprehend diuresis, cardiotonic, analgesia, neuralgia, gout and, furthermore, even neoplastic effect. The components of aconitum have been acknowledged as aconitine, mesaconitine, hypaconitine, aconine and so on. The main ingredient, aconitine has the advantage of causing the atrial fibrillation, but, its pharmacological research has not been fully elucidated. Although there are many reports with regard to the pharmacological effects on the motility of several animal hearts, their conclusions have not been regretfully coincided yet. The authors hereby paid attention to this point of view and made experiment to examine the relationship between the alcohol extract of Korean aconitum and the motility of the isolated clam heart, making the use of several drugs related to the heart such as serotonin, acetylcholine, pilocarpine, physostigmine, barium chloride, procaine and quinidine. The cardiac movement of the isolated clam (Meretrix lusoria) heart in the standard sea water solution was recorded with the electric kymograph according to the Magnus method. The results of the experiment are as follows. 1. The motility of the isolated clam heart represents the tendency of gradual inhibition in proportion to the concentration of AK-A 10-4, 5 X 10-4, and 10-3. 2. The cardiac inhibitory effect of AK-A 10-3 antagonizes the motility of the isolated clam heart pretreated with serotonin 10-6. 3. The cardiac inhibitory effect of AK-A 10-3 antagonizes the systolic state appealed by barium chloride 10-3. 4. The systolic state caused by quinidine 10-4 is not inhibited by AK-A 10-3.

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