Responsiveness of Muscarinic and Alpha Adrenergic Activation on Endothelial Cell in Isolated Canine Renal Arteries

정수연,장기철,임정규,Chung, Soo-Youn,Chang, Ki-Churl,Lim, Jung-Kyoo The Korean Society of Pharmacology 1989 대한약리학잡지 Vol.25 No.1

Responsiveness of muscarinic and alpha adrenoceptor activation on endothelial cells was studied in isolated canine renal artery rings. Ach (10-100 nM), dose dependently, relaxes endothelial intact rings precontracted with phenylephrine ($IC_{50}$ of Ach was 34.5 nM). Selective mechanical destruction of the endothelium transformed the activity of this substance from vasodilatation to vasoconstriction. Acetylcholine induced relaxations could be selectively inhibited competitively by atropine, but could not be inhibited by cyclooxygenase inhibitor. Methylene blue, however, an inhibitor of soluble guanylate cyclase activity, inhibited Ach as well as sodium nitroprusside (SNP) induced relaxation. Relaxation produced by prostacyclin was not modified by methylene blue. On the other hand, alpha adrenoceptor agonist did not relax but contract canine renal artery rings possessing an intact intima precontracted with U-46619. Clonidine, however, selective alpha-2 adrenergic agonist, is more susceptible than phenylepherine, selective alpha-1 adrenergic agonist, to the inhibitory effect of contraction. These results suggest that in canine renal artery rings, 1) muscarinic receptor is responsible for releasing endothelium dependent relaxation factor (EDRF). 2) alpha-1 and alpha-2 adrenergic receptors are present in canine renal artery. 3) relaxation via EDRF is antagonized by methylene blue, providing further evidence that EDRF acts through a cGMP mechanism. 내피세포가 잘 보존된 개 신동맥에서 Phenylephrine으로 전 수축시킨 후 Actylcholine을 투여하면 혈관 이완을 관찰할 수 있었지만 내피세포를 파괴시킨 개 신동맥에서는 혈관 이완을 관찰할 수 없었으므로 내피세포가 혈관 이완에 관여함을 알 수 있었다. 그래서 내피세포에서 분비되어 혈관 이완을 촉진하는 물질을 Endothelium Dependent Relaxation Factor (EDRF)라고 한다. Acetylcholine에 의한 혈관 이완은 Atropine에 의해 경쟁적으로 억제되었으므로 Muscarinc 수용체의 자극을 받아 EDRF가 분비되고 이것이 평활근에 작용하여 이완을 일으킬 것으로 생각되었다. EDRF의 작용기전을 알아보기 위해 용해성 Guanylate cyclase 억제제인 Methylene blue를 전처치 했을 때는 Acetylcholine 뿐 만 아니라 Sodium nitroprusside에 의한 이완도 억제되었다. 그러나 Prostacyclin에 의한 이완은 억제되지 않았다. 이 결과로 판단 해 보면 EDRF에 의한 이완효과가 Cyclic GMP와 관련이 있을 것으로 생각되었다. 한편 Thromboxane $A_2$ 유사체인 U-46619로 전수축 시킨 후 Alpha-2 아드레날린성 항진제인 Clondine을 투여했을 때 혈관 이완은 일어나지 않았다. 수축의 억제 양상에 있어서 Alpha-1 아드레날린성 항진제인 Phenylephrine보다 Clonidine이 더 효과적 이었다. 이상의 결과를 기초로 하여 다음과 같은 결론을 얻을 수 있었다. 1) Muscarinic 수용체의 자극을 받아 EDRF의 분비가 촉진된다. 2) Alpha-1 아드레날린성 수용체와 Alpha-2 아드레날린성 수용체가 개 신동맥에 존재한다. 3) EDRF에 의한 이완이 Methylene blue에 의해서 억제되므로 cGMP를 이용한 기전 임을 알 수 있었다.단요수근신건과 외상과의 변화를 알 수 있으며 진단에 있어서 보조적인 역할을 할 수 있다. 하지만, 치료 후 증상 호전 도달기간의 예후 판정에는 크게 도움이 되지 않는다. 시술과정에서 코일의 이탈이 2예에서 발생하였으나, 모두 snare기법으로 제거되었고, 그 밖의 다른 합병증은 없었다. 결론: 만성골반통을 일으키는 골반울혈증후군의 치료에 있어서 코일을 이용한 난소정맥색전술은 단기추적검사상 다수에서 증상의 소실 및 완화를 보여 비교적 효과적이고 안전한 방법으로생각되며, 다른 병인이 공존하지 않는다면 기존의 수술적 치료를 대치할 수 있는 훌륭한 중재적 치료법으로써 이용될 수 있을 것으로 사료된다. 있게 큰 수치를 보였다. 결론: 정상 두개내혈관 직경은, 성별 차이가 40대에서 분명하였고 남자가 여자에 비하여 크거나 큰 경향을 보였으며, 중뇌동맥 직경은 성별에 상관없이 고령층이 저령층에 비하여 의미있게 크거나 큰 경향을 나타내었다. 고령층의 중뇌동맥 근위부 직경은 남자가 2.59$\pm$0.35 mm, 여자가 2.38$\pm$0.37 mm이었고, 원위부 직경은 남자가 2.63$\pm$0.43 mm, 여자가 2.39$\pm$0.35 mm 이었다.고 Monaliza Finely Soft는 23% 더 높은 분리율을 나타냈으므로 선충분리용(線蟲分離用)으로는 향수처리(香水處理)되지 않은 것이 더 좋은 것으로 사료(思料)된다. 4. 온도별(溫度別) 선충분리율(線蟲分離率)을 $15^{\circ},\;25^{\circ}\;and\;35^{\circ}C$에서 조사(調査)한 결과(結果) 전체적(全體的)으로 $35^{\circ}C$에서 분리율(分離率)이 가장 높게 나타났다. 5. 시간경과(時間經過)에 따른 선충분리율(線蟲分離率)은 12시간(時間) 후(後)가 35.3 %이고 24시간(時間) 후(後)가 40.

오수유가 선천성고혈압흰쥐의 혈압에 미치는 영향

정수연(Soo Youn Chung),박윤주(Youn Joo Park),정면우(Myeon Woo Chung),임화경(Hwa Kyung Lim),강주희(Ju Hee Kang),최기환(Ki Hwan Choi),김주일(Joo Il Kim) 한국응용약물학회 2000 Biomolecules & Therapeutics(구 응용약물학회지) Vol.8 No.4

The present study examined the effect of a methanol extract of Evodiae Fructus on the blood pressure in spontaneously hypertensive rats (SHR). The systolic blood pressure was measured after rats were pretreated with phentolamine, propranolol, or N_ω-nitro-_L-arginine methyl ester(NAME) and subsequently received methanol extract of Evodiae Fructus. In SHR, intraperitoneal administration of methanol extract of Evodiae Fructus (0.5 mg/kg) produced antihypertensive effect that lasted for at least 4 hours. Antihypertensive effect of Evodiae Fructus was more stronger than that with α-adrenergic receptor antagonist phentolamine and was not affected by β-adrenergic receptor antagonist propranolol. The antihypertensive effect of Evodiae Fructus was abolished by pretreatment of NAME. Our findings suggest Evodiae Fructus has an hypertensive effect, which may be mediated through nitric oxide synthesis.

개 신동맥 내피세포의 무스카린성 및 알파 아드레날린성 수용체에 대한 작용

정수연(Soo Youn Chung),장기철(Ki Churl Chang),임정규(Jung Kyoo Lim) 대한약리학회 1989 대한약리학잡지 Vol.25 No.1

내피세포가 잘 보존된 개 신동맥에서 Phenylephrine으로 전 수축시킨 후 Actylcholine을 투여하면 혈관 이완을 관찰할 수 있었지만 내피세포를 파괴시킨 개 신동맥에서는 혈관 이완을 관찰할 수 없었으므로 내피세포가 혈관 이완에 관여함을 알 수 있었다. 그래서 내피세포에서 분비되어 혈관 이완을 촉진하는 물질을 Endothelium Dependent Relaxation Factor (EDRF)라고 한다. Acetylcholine에 의한 혈관 이완은 Atropine에 의해 경쟁적으로 억제되었으므로 Muscarinc 수용체의 자극을 받아 EDRF가 분비되고 이것이 평활근에 작용하여 이완을 일으킬 것으로 생각되었다. EDRF의 작용기전을 알아보기 위해 용해성 Guanylate cyclase 억제제인 Methylene blue를 전처치 했을 때는 Acetylcholine 뿐 만 아니라 Sodium nitroprusside에 의한 이완도 억제되었다. 그러나 Prostacyclin에 의한 이완은 억제되지 않았다. 이 결과로 판단 해 보면 EDRF에 의한 이완효과가 Cyclic GMP와 관련이 있을 것으로 생각되었다. 한편 Thromboxane A₂ 유사체인 U-46619로 전수축 시킨 후 Alpha-2 아드레날린성 항진제인 Clondine을 투여했을 때 혈관 이완은 일어나지 않았다. 수축의 억제 양상에 있어서 Alpha-1 아드레날린성 항진제인 Phenylephrine보다 Clonidine이 더 효과적 이었다. 이상의 결과를 기초로 하여 다음과 같은 결론을 얻을 수 있었다. 1) Muscarinic 수용체의 자극을 받아 EDRF의 분비가 촉진된다. 2) Alpha-1 아드레날린성 수용체와 Alpha-2 아드레날린성 수용체가 개 신동맥에 존재한다. 3) EDRF에 의한 이완이 Methylene blue에 의해서 억제되므로 cGMP를 이용한 기전 임을 알 수 있었다. Responsiveness of muscarinic and alpha adrenoceptor activation on endothelial cells was studied in isolated canine renal artery rings. Ach (10-100 nM), dose dependently, relaxes endothelial intact rings precontracted with phenylephrine (IC₅₀ of Ach was 34.5 nM). Selective mechanical destruction of the endothelium transformed the activity of this substance from vasodilatation to vasoconstriction. Acetylcholine induced relaxations could be selectively inhibited competitively by atropine, but could not be inhibited by cyclooxygenase inhibitor. Methylene blue, however, an inhibitor of soluble guanylate cyclase activity, inhibited Ach as well as sodium nitroprusside (SNP) induced relaxation. Relaxation produced by prostacyclin was not modified by methylene blue. On the other hand, alpha adrenoceptor agonist did not relax but contract canine renal artery rings possessing an intact intima precontracted with U-46619. Clonidine, however, selective alpha-2 adrenergic agonist, is more susceptible than phenylepherine, selective alpha-1 adrenergic agonist, to the inhibitory effect of contraction. These results suggest that in canine renal artery rings, 1) muscarinic receptor is responsible for releasing endothelium dependent relaxation factor (EDRF). 2) alpha-1 and alpha-2 adrenergic receptors are present in canine renal artery. 3) relaxation via EDRF is antagonized by methylene blue, providing further evidence that EDRF acts through a cGMP mechanism.

오수유가 N-nitro-L-arginine methyl ester로 유발한 고혈압흰쥐의 심혈관계에 미치는 영향

정수연(Soo Youn Chung),이숙영(Sook Young Yi),유태무(Tae Moo Yoo),안미령(Mee Ryung Ahn),최현진(Hyun Jin Choi),정면우(Myeon Woo Chung),류항묵(Hang Mook Rheu),양지선(Ji Sun Yang) 대한약학회 1999 약학회지 Vol.43 No.3

The present study examined the effect of a methanol extract of Evodiae Fructus on the cardiovascular function in N-nitro-L-arginine methyl ester (NAME)-induced hypertensive Wistar rats after treatment over 6 weeks. In rats treated with NAME, blood pressure, weight of heart, aorta media thickness and media/lumen ratio significantly (p<0.05) increased, whereas coronary flow and heart rate of isolated heart significantly (p<0.05) decreased compared with control group at 6 weeks. In rats treated with NAME and Evodiae Fructus, blood pressure, aorta media thickness and media/lumen ratio signiflcantly(p<0.05) decreased compared with NAME treated group at 6 weeks. These results suggest that Evodiae Fructus is applicable to the treatment of hypertension and vascular hypertrophy.

홍화씨의 경골골절치유에 미치는 영향

정수연(Soo Youn Chung),최현진(Hyun Jin Choi),정면우(Myeon Woo Chung),안미령(Mee Ryung Ahn),유태무(Tae Moo Yoo),류항묵(Hang Mook Rheu),양지선(Ji Sun Yang) 대한약학회 1999 약학회지 Vol.43 No.4

We investigated the effect of safflower-seed on fracture healing of fracture model in rat. Fracture healing was evaluated by examining the degree of wound healing macroscopically, radiography, bone histomorphometry and biochemical examination. After 1,3,5,7 days, the wound healing was accelerate in safflower-seed diet group. Radiography does not reveal the difference in fracture healing between two groups. After 2 weeks, safflower-seed had a significant, stimulatory effect on external callus formation(p<0.05). But after 4,6,8 weeks, no difference was observed between normal and safflower-seed diet group in callus size. Urinary hydroxyproline, osteocalcin and total alkaline phosphatase decreased significantly (p<0.05) in safflower-seed treated group at 2 week after fracture.

죽염의 약리작용 평가

정수연(Soo Youn Chung),이숙영(Sook Young Yi),류항묵(Hang Mook Rheu),양지선(Ji Sun Yang),유태무(Tae Moo Yoo),김옥희(Ok Hee Kim),노용남(Yong Nam Roh),정면우(Myeon Woo Chung),안미령(Mee Ryung Ahn),최현진(Hyun Jin Choi) 한국응용약물학회 1999 Biomolecules & Therapeutics(구 응용약물학회지) Vol.7 No.2

Bamboo salt has been used for the purpose of precaution and treatment of certain diseases including cancer. Therefore, present study was carried out to ascertain the effects of bamboo salt upon anti-cancer, anti-hypertensive, and anti-diabetic activities as well. To examine the anti-cancer activity of bamboo salt, ICR mice implanted with 1 X 10^6 cells of sarcoma 180 intraperitoneally had been treated daily with bamboo salt A, crude salt, and reagent-grade NaCl (0.2, 1.0, and 2.0 g/kg, p.o.) for 60 days using adriamycin (2 mg/kg) as a positive control. Neither survival rate nor body weight had been significantly influenced by all the treatments indicating that bamboo salt A did not exert the anti-cancer effect on ICR mice. Anti-hypertensive activity was examined in spontaneously hypertensive rats (SHR) which had been administered with bamboo salt A, crude salt, and reagent-grade NaCl (0.1, 0.5, and 1.0 % in drinking water) for 28 days using hydralazin (2 mg/kg) as a positive control. Blood pressure and heart rate were measured at 1, 3, and 4 weeks after the starting date. Significant anti-hypertensive activity was not observed in any treated group compared to the positive control group. In order to determine if bamboo salt had anti-diabetic activity, rats in which diabetes had been induced by streptozotocin (45 mg/kg, i.m.) were treated daily with bamboo salt A, crude salt, and reagent-grade NaCl (0.2, 1.0, and 2.0 g/kg, p.o.) for 28 days using insulin (50 U/kg, s.c.) as a positive control. Blood samples were taken and analyzed at 1, 2, and 4 weeks after the starting date. Bamboo salt did not cause any decreasing effect on the blood glucose levels. These results clearly demonstrated that bamboo salt A did not exert anti-cancer, anti-hypertensive, or anti-diabetic activities in the present experimental animals.

난소절제 흰쥐에서 Estrogen의 항비만 효과

정수연(Soo Youn Chung),유태무(Tae Moo Yoo),양지선(Ji Sun Yang),류항묵(Hang Mook Rheu) 대한약학회 1999 약학회지 Vol.43 No.1

Obesity is a chronic disease that is increasing in prevalence and that poses a serious risk for the hypertension, osteoporosis, heart disease, diabetes mellitus and certains forms of cancer. This study was performed to develop of obesity animal model and to assess the pharmacological assay for the rats of 8 weeks or 4 days after ovariectomization treated with estradiol for 8 weeks on the body weight, fat weight and food intake. The body weight, fat weight and food intake increased in the ovariectomized rats. In the rat of 8 weeks after ovariectomization treated with estradiol (250mg/100g) 8 weeks, the body weight decreased significantly (p<0.05). In the rats of 4 days after ovariectomization treated with estradiol 8 weeks, the body weight decreased significantly (p<0.05). These results suggest that estrogen plays a role in regulation body weight response to food intake and fat weight.

국제학술 Symposium 논문집 : 국내 생물학적동등성시험 현황

정수연(Soo Youn Chung) 서울시립대학교 산업기술연구소 2002 국제학술SYMPOSIUM논문집 Vol.10 No.1

중국, 일본, 한국, WHO의 한약 자발적부작용보고체계 현황

우연주,정수연,박병주,Woo, Yeon-Ju,Chung, Soo-Youn,Park, Byung-Joo 대한한방내과학회 2014 大韓韓方內科學會誌 Vol.35 No.2

Drugs may cause adverse effects, and spontaneous adverse drug reaction (ADR) reports have been used as the main method of drug safety evaluation after drugs have been released. The World Health Organization (WHO) collects ADR data reported from pharmacovigilance organizations in each nations. In China, pharmacovigilance centers operate with hierarchical structure at local, provincial and national levels. Also, Japan and Korea each operate their own respective independent pharmacovigilance organizations. WHO is collecting ADR reports for herbal medicine and 15~20% of all ADRs was related to herbal medicine in China. There are status reports of ADRs for herbal medicine in Japan as well. However, in Korea, there is no ADR reporting system regarding herbal medicine. In light of these overseas cases, a spontaneous ADR reporting system for herbal medicine in Korea should be necessary as well.

한국재래산양 태아 및 신생아 척수에서 GFAP 면역반응세포에 관한 형태학적 연구

송치원,정수연,이근좌,이강이,이경열,박일권,박미선,정승혁,조규완,김무강,Song, Chi-Won,Chung, Soo-Youn,Lee, Keun-Jwa,Lee, Kang-Iee,Lee, Kyoung-Youl,Park, Il-Kwon,Park, Mi-Sun,Chung, Seung-Hyuk,Cho, Gyu-Woan,Kim, Moo-Kang 대한수의학회 2001 大韓獸醫學會誌 Vol.41 No.4

Glial fibrillary acidic protein(GFAP) is one of the intermediate filaments, and used as an astrocyte detection marker. GFAP distribution has been studied on the fetal, neonatal and aged brains. In this study, the GFAP immunoreactive cell localization and distribution in the fetal (30, 45, 60, 90, 105 and 120 days of gestation) and neonate spinal cords of Korean native goat were investigated by immunohistochemistry. Nonpolar radial glial cells initiated to appear at 45 days of gestation. GFAP-immunoreactive processes were extended from central canal to pia matter. Bipolar immumoreactive cells were transformed to monopolar and multipolar immunoreactive cells at 45 days of gestation. Multipolar astrocytes of 60 days of gestation were found within white and gray matters of spinal cord. The number of GFAP-immunoreactive cells were gradually decreased from 90 days of gestation until newborn neonate. The intensity of GFAP immunoreactivity was gradually decreased from 95 days of gestation until newborn neonate. These results suggest that the radial glial cells within the gray and white matters of spinal cord are very fast developed.