• 동국한의학연구소논문집
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• 제8권1호
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• pp.107-116
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• 1999

이 실험의 목적은 소속명탕(小續命湯)에 대하여 KCN(potassium cyanide)으로 유발된 혼수시간과 생존시간을 측정하여 전뇌허혈(全腦虛血)에 미치는 영향을 관찰하고, 또한 MCA occlusion 유발시 뇌부종율(腦浮腫率)과 뇌허혈면적(腦虛血面積)을 측정하여 국소뇌허혈(局所腦虛血)에 미치는 영향을 실험연구하였다. 1. 전뇌허혈 유발실험에서 유의성있는 KCN 유발 혼수시간의 단축, 치사량의 KCN에 대한 생존시간의 연장 효과가 나타났다. 2. 국소 뇌허혈 유발실험(MCA occlusion)에 미치는 효과에서는 뇌허혈면적과 뇌부종율이 대조군에 비하여 유의성있게 감소하였다.

• 대한한의학원전학회지
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• 제28권2호
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• pp.103-114
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• 2015

Objectives : The publication year(1608) of Euilinchwalyo is very closed to the year(1610) of Dongeuibogam, so several researches indicate that Dongeuibogam was influenced by Euilimchwalyo. We, authors have recently focused on the way to quote books in Dongeuibogam and found particular aspects in the way of quotation between Euilimchwalyo and Dongeuibogam. Methods : 1. Comparing the contents of Sosokmyeongtang in quotation books between Euilimchwalyo and Dongeuibogam. 2. Tracing the origin of Sosokmyeongtang and comparing chief virtue, consist of herbal medicine, way of dose and making and the method of addition and subtraction in Sosokmyeongtang. Results : Beijiqianjiyaofang was the origin book that recorded Sosokmyeongtang but there was no methods of addition and subtraction. After Jin and Yuan dynasty, the books, which had Sosokmyeongtang, started to record the methods of addition and subtraction in Sosokmyeongtang. However, even though Euilinchwalyo also recorfed the methods of addition and subtraction in Sosokmyeongtang such as other medical books, Dongeuibogam didn't keep that way to document up. Conclusions : The fact that Dongeuibogam was influenced by Euilimchwalyo means 2 ways. The first is that Dongeuibogam was influenced by Euilimchwalyo directly. The second is that Heo Jun, who wrote Dongeuibogam, tried not to duplcate or follow Euilimchwalyo somehow.

• 대한한방내과학회지
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• 제35권3호
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• pp.298-308
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• 2014

Objectives: In this study we made an effort to investigate the protective effect of SSMT on the N-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) -induced cytotoxicity of SH-SY5Y cells. Methods: The cell viability was assessed by 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide (MMT) assay. The fluorescence intensity was measured by using a dye and then with propidium iodide (PI) DNA flow cytometry analysis of the effects on the cell cycle of the SH-SY5Y cells and were used to measure the fluorescence of intracellular reactive oxygen species generation by MPTP. Results: Pretreatment of SSMT significantly suppressed MPTP-induced cytotoxicity, which was revealed as apoptosis characterized by the reduction of cell viability, the increase of ROS production, and the loss of mitochondrial membrane potential in SH-SY5Y cells. Conclusions: These findings suggest that SSMT exerts neuroprotective effects on human neuroblastoma SH-SY5Y cells by MPTP-induced dopaminergic neurodegeneration.

• 대한한방내과학회지
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• 제21권5호
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• pp.851-857
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• 2000

SosokMyeongTang(SMT) have been used in oriental medicine for many centuries as a therapeutic agent for cerebral disease. The effects of SMT on the vascular system is not known. The purpose of this study was to investigate the effects of SMT on the changes in blood pressure(BP) and regional cerebral blood flow(rCBF) of rats. SMT consists of the following components : Radix Ledebouriellae(防風), Radix Cocculi or Stephaniae(防己), Semen Armeniacae(杏仁), Cortex Cinnamomi(肉桂), Radix Scutellariae(黃芩), Radix Paeoniae Lactiflorae(白芍藥), Radix Ginseng(人蔘), Rhizoma Cnidll(川芎), Herba Ephedrae(麻黃), Radix Glycyrrhizae(甘草), Radix Aconiti(附子?), Fructus Zizyphi Jujubae(大棗), Rhizoma Zingiberis(生薑) and the changes of BP and rCBF were tested Leser-Doppler Flowmetry(LDF) The experimental results were as follows ; BP was not affected by SMT in rats, but rCBF was increased significantly by SMT in a dose dependent manner. SMT increased previous decreasd rCBF due to pretreatment methylene blue, but did not increased previous decreasd rCBF due to pretreatment L-NNA, indomethacin. Pretreatment with indomethacin decreased BP compaired with control group. These results suggest that SMT causes a diverse response of blood pressure and regional cerebral blood flow(rCBF). The increased rCBF is mediated by nitric oxide synthease.

• 한방재활의학과학회지
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• 제21권4호
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• pp.49-65
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• 2011

Objectives: This study was performed to investigate the effects of Gagamsosokmyeong-tang(Jiajianxiaoxuming-tang) on the monosodium iodoacetate(MIA) induced early state osteoarthritis in rats. Methods: Osteoarthritis was induced by injection of MIA(0.25 mg) into knee joints of rats. Osteoarthritis rats were divided into control(n=8) and treated=8 group respectively, Control group was taken distilled water and treated group was taken extracts of Gagamsosokmyeong-tang(Jiajianxiaoxuming-tang) by orally for 20 days. Body weight was measured at 0, 5, 10, 15, 20 days after MIA injection. At the end of experiment, gross and histopathological examination on the articular cartilages of the knee joints were performed. Proteoglycan(PG) content of articular cartilages were analysed by safranine O staining method. The content of tumor necrosis $factor-{\alpha}(TNF-{\alpha})$, $interleukin-1{\beta}(IL-1{\beta})$ in synovial fluids were analysed by enzyme-inked inmunosorbent assay(ELISA) method. And also cycloxygenase-2(COX-2), matrix metalloproteinase 3(MMP-3), inducible nitric oxide synthase(iNOS), calpain immunochistochemical examination on the knee joints were performed. Results: PG content in articular cartilages of the treated group was significantly increased compared with control group. Histopathological osteoarthritic score of the treated group was significantly decreased compared with control group. $TNF-{\alpha}$ content in synovial fluids, expression of iNOS and calpain in synovial membrane of the treated group were significantly decreased compared with control group. But body weight, $1L-1{\beta}$ content in synovial fluids, expression of iNOS and MMP-3 of the treated group were not significantly changed compared with control group. Conclusions: On the basis of these results, we conclude that Gagamsosokmyeong-tang(Jiajianxiaoxuming-tang) has anti-arthritic effects on the MIA induced early stage osteoarthritis in rats.