TY - JOUR
T1 - Antihypertensive effect of synthetic tetrandrine derivatives in SHR rats
AU - Kawashima, Koichiro
AU - Hayakawa, Terumasa
AU - Hisayo, Oohata
AU - Fujimoto, Kazuko
AU - Suzuki, Takeshi
AU - Ogino, Tatsunori
AU - Chen (Masao Chin), Zhengxiong
PY - 1991
Y1 - 1991
N2 - 1. 1. Effects of oral administration of synthetic tetrandrine (TD) derivatives (20 mg/kg per day) for 9 weeks on blood pressure, heart rate, plasma renin concentration (PRC) and vascular reactivities to pressor substances were studied in spontaneously hypertensive (SHR) rats. 2. 2. 7-O-Ethyl fangchinolin (7-O-EFC) and 7-O-isopropyl fangchinolin (7-O-IFC) produced a significant and sustained reduction in blood pressure from the first week of administration. 7-O-EFC reduced heart rate when determined under restraint conditions, but not under unanesthetized, freely moving conditions. 3. 3. TD derivatives produced no effect on PRC. 4. 4. Pressor response to phenylephrine was reduced significantly whereas the response to angiotensin II was enhanced after prolonged administration of 7-O-EFC and 7-O-IFC. 5. 5. These results demonstrate that TD derivatives are potential antihypertensive drugs, and that attenuation of the pressor response to phenylephrine may contribute at least in part to its antihypertensive effect.
AB - 1. 1. Effects of oral administration of synthetic tetrandrine (TD) derivatives (20 mg/kg per day) for 9 weeks on blood pressure, heart rate, plasma renin concentration (PRC) and vascular reactivities to pressor substances were studied in spontaneously hypertensive (SHR) rats. 2. 2. 7-O-Ethyl fangchinolin (7-O-EFC) and 7-O-isopropyl fangchinolin (7-O-IFC) produced a significant and sustained reduction in blood pressure from the first week of administration. 7-O-EFC reduced heart rate when determined under restraint conditions, but not under unanesthetized, freely moving conditions. 3. 3. TD derivatives produced no effect on PRC. 4. 4. Pressor response to phenylephrine was reduced significantly whereas the response to angiotensin II was enhanced after prolonged administration of 7-O-EFC and 7-O-IFC. 5. 5. These results demonstrate that TD derivatives are potential antihypertensive drugs, and that attenuation of the pressor response to phenylephrine may contribute at least in part to its antihypertensive effect.
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U2 - 10.1016/0306-3623(91)90328-4
DO - 10.1016/0306-3623(91)90328-4
M3 - Article
C2 - 2050283
AN - SCOPUS:0026056856
SN - 0306-3623
VL - 22
SP - 165
EP - 168
JO - General Pharmacology
JF - General Pharmacology
IS - 1
ER -