1.Verapamil and propranolol in the control of mild to moderate systemic hypertension
Journal of Medical and Pharmaceutical Information 1999;2():26-30
The antihypertensive effects of verapamil and propranolol were evaluated in 62 patients with mild to moderate systemic hypertension. We also studied the change of 24 hours urinary catecholamines. 31 cases received verapamil and 31 others were treated by propranolol for 4 weeks. Before treating, there were no statistically significant differences (ECG, echocardiology, blood pressure...) noted between the two groups. Conclusions: 1) Blood pressure and heart rate were controlled by verapamil as well as by propranolol. 2) 24 hours urinary catecholamines were reduced by verapamil but not by propranolol
Hypertension
;
Verapamil
2.Intravenous Verapamil for Reversal of Refractory Coronary Vasospasm and Cardiac Arrest.
Kwang Kon KOH ; Sun Soo PARK ; Sang Hoon LEE ; Heung Kon HWANG ; Pan Gum KIM ; Yeon Hyeon CHOE
Korean Circulation Journal 1991;21(4):700-705
No abstract available.
Coronary Vasospasm*
;
Heart Arrest*
;
Verapamil*
3.Effects of endotoxin and verapamil on superoxide production by rat alveolar macrophage.
Choon Taek LEE ; Keun Youl KIM
Tuberculosis and Respiratory Diseases 1993;40(3):223-235
No abstract available.
Animals
;
Macrophages, Alveolar*
;
Rats*
;
Superoxides*
;
Verapamil*
4.Effects of Intravenous Verapamil on Paroxysmal Supraventricular Tachycardia.
Seung Jung BAHK ; Woong Ku LEE ; Seung Yun CHO ; Won Heum SHIM
Korean Circulation Journal 1985;15(3):447-453
Verapamil is highly effective in terminating paroxysmal supraventricular tachycardia(PSVT) by its depressive action on the AV node. In other countries it is already the drug of choice if vagal manevers fail for conversion of PSVT. We evaluated therapeutic efficacy of intravenous verapamil in 30 patients with PSVT who visited Severance Hospital from november 1978 to November 1984. Twenty six of 30 patients(86.7%) had a restoration of normal sinus rhythm by intravenous verapamil without significant side effects. Thus intravenous verapamil is safe and extremely effective in terminating most PSVT.
Atrioventricular Node
;
Humans
;
Tachycardia, Supraventricular*
;
Verapamil*
5.Effects of verapamil and allopurinol on ischemia-reperfusion injury in rat liver.
Young Hyun LEE ; Jae Dong CHEON ; Joo Seop KIM ; Gu KANG ; Soo Tong PAI
Journal of the Korean Surgical Society 1993;45(3):307-313
No abstract available.
Allopurinol*
;
Animals
;
Liver*
;
Rats*
;
Reperfusion Injury*
;
Verapamil*
6.The effect of verapamil and urokinase on hepatocyte function and systemic hemodynamics in acute liver ischemia.
Bo Yang SUH ; Dong Kwun SUH ; Joo Hyung LEE ; Woo Seok SUH ; Ho Yeol YE ; Hong Jin KIM ; Min Chul SHIM ; Koing Bo KWUN ; Dong Il PARK
Journal of the Korean Surgical Society 1993;44(1):11-23
No abstract available.
Hemodynamics*
;
Hepatocytes*
;
Ischemia*
;
Liver*
;
Urokinase-Type Plasminogen Activator*
;
Verapamil*
7.Intralesional Injection of Verapamil Only and Verapamil and Serial Triamcinolone Acetonide in Peyronie's Disease.
Korean Journal of Urology 2000;41(8):999-1003
No abstract available.
Injections, Intralesional*
;
Male
;
Penile Induration*
;
Triamcinolone Acetonide*
;
Triamcinolone*
;
Verapamil*
8.Effects of verapamil, tamoxifen and cyclosporin A for the modulation of multidrug resistance in human lung cancer lines.
Joo Hang KIM ; Byung Soo KIM ; Jung Joo CHOI ; Kyung Mi KIM ; Nae Choon YOO ; Jin Hyuk CHOI ; Ho Young LIM ; Jae Kyung ROH ; Kyung Sik LEE ; Byung Soo KIM
Journal of the Korean Cancer Association 1993;25(2):225-235
No abstract available.
Cyclosporine*
;
Drug Resistance, Multiple*
;
Humans*
;
Lung Neoplasms*
;
Lung*
;
Tamoxifen*
;
Verapamil*
9.Isolation of Putative Limbal Epithelial Stem Cells by Fluorescein Activated Cell Sorting.
Mee Kum KIM ; Kyeong Seon SHIN ; Gyung Ah JUNG ; Ki Cheul SHIN ; Won Ryang WEE ; Jae Lim LEE ; Ki Sook PARK ; Young Sook SON
Journal of the Korean Ophthalmological Society 2005;46(3):521-527
PURPOSE: To analyze the isolating pattern of slow cycling cells as putative limbal epithelial stem cells (PLESCs) using Hoechst exclusive cell sorting. METHODS: Rabbits were injected with 5-bromo-2-deoxyuridine (Brd U) 1 month prior to be sacrificed. After obtaining limbal tissues, fluorescence-activated cells were sorted on a Coulter EPICS 753 after they had been incubated with Hoechst 33342 and propidium iodide. Two different methods were applied to sort PLESCs. Side-population(Sp) cells were obtained using gates with dichroic mirror to detect low Hoechst blue and red after verapamil was treated. Hoechst negative cells were obtained using gates exhibiting low Hoechst blue with a 424/44 BP filter. Brd U-retaining cells were counted and their sizes were evaluated in each gated sample to compare isolating pattern of PLESCs in each method. RESULTS: The percentages of Sp cells and of the Hoechst negative fraction were 0.96 +/- 0.79% and 16.01 +/- 13.60%, respectively(p=0.021). Homogeneity and density of the small cells were higher in Hoechst negative fraction than in Sp cells. The percentage of Brd U-retaining cells was 47.36 +/- 10.34% and 47.14 +/- 14.94% in Sp cells and Hoechst negative fraction, respectively(p>0.05), and they were 10 times higher than in non-Sp and Hoechst positive fraction(p=0.000). CONCLUSIONS: Hoechst negative exclusion without verapamil more efficiently isolated PLESCs than Sp did.
Cornea
;
Epithelium
;
Fluorescein*
;
Propidium
;
Rabbits
;
Stem Cells*
;
Verapamil
10.Chronotropic Actions of Higenamine in the Isolated Right Atrium of the Rabbit.
Chung Il NOH ; Chang Yee HONG ; Bong Ki KIM ; Chan Woong PARK ; Jung Kyoo LIM
Korean Circulation Journal 1988;18(2):277-285
Higenamine is known to possess stimulatory activity on beta-receptor of the heart. Chronotropic actions of higenamic were studied in spontaneously beating right atrial muscle isolated from rabbits. The frequency of spontaneous beating and the relative threshold voltage of the right atrium were examined. The relative threshold voltage was defined as the minimal voltage of the given impulse above which the right atrium could be paced at the frequency of 20% of higenamine was also observed. Higenamine caused the postive chronotropic effect. This response became prominent as the ca2+ concentration in the bathing solution lowered. When tetrodotoxin was added to the bathing solution, the effect of higenemine altered and became similar to that of epinephrine. Higenamine reduced the relative threshold voltage of the right atrium in the bathing solution with [ca2+] of 0.5mM. Such effect was abolished by tetrodotoxin. The effects of verapamill on the spontaneous rate and the relativel threshold voltage were inhibited by higenemine. The above results suggest that, aithough the main action og higenamine is on the Ca channel, higenamine also have a minor effect of augmenting the Na channel.
Baths
;
Epinephrine
;
Heart
;
Heart Atria*
;
Heart Rate
;
Rabbits
;
Tetrodotoxin
;
Verapamil