| Project/Area Number |
09672047
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Surgical dentistry
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| Research Institution | Osaka University |
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Principal Investigator |
NIWA Hitoshi (1998) Department of Osaka University, Faculty of Dentistry, associate professor, 歯学部, 助教授 (30218250)
金 容善 (1997) 大阪大学, 歯学部・附属病院, 講師 (20252695)
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| Co-Investigator(Kenkyū-buntansha) |
丹羽 均 大阪大学, 歯学部・附属病院, 講師 (30218250)
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| Project Period (FY) |
1997 – 1998
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| Project Status |
Completed (Fiscal Year 1998)
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| Budget Amount *help |
¥2,500,000 (Direct Cost: ¥2,500,000)
Fiscal Year 1998: ¥500,000 (Direct Cost: ¥500,000)
Fiscal Year 1997: ¥2,000,000 (Direct Cost: ¥2,000,000)
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| Keywords | EPINEPHRINE / β BLOCKER / HEMODYNAMICS / SPONTANEOUSLY HYPERTENSIVE RATS / 相互作用 |
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| Research Abstract |
We investigated the effects of the interaction between nonselective β adrenergic blocking agents and epinephrine on the hemodynamics in spontaneously hypertensive rats (SHR) and Wistar Kyoto rats (WKY).
(Study 1) : Nonselective β blocker, pindolol, and 2% lidocaine containing 1:80,000 epinephrine were administered to conscious SHR and WKY intraperitoneally Blood pressures and heart rate were measured by the photoplethysmografic tail cuff method. Epinephrine did not cause significant hemodynamic changes in WKY after the pindolol pretreatment. On the other hand, blood pressure increased significantly in SHR. From these observation, it was suggest that a effects of epinephrine on peripheral vascular bed was exaggerated in the presence of pindolol.
In an additional study, fenylephrine was administered to SHR and WKY intraperitoneally. There was more marked increase in blood pressure in SHR than WKY. This result showed that SHR was more sensitive to a stimulator than WKY.
(Study 2) : Under general anesthesia with propofol, nonselective β blocker, ploplanolol was injected intravenous. Then epinephrine was injected intravenous continuously to SHR and WKY. Blood pressure and heart rate were measured invasively through the femoral artery. We found that in both SHR and WKY, epinephrine in combination with proplanolol induced remarkable increase in blood pressure. From these observation, it was suggest that a effects of epinephrine on peripheral vascular bed was exaggerated in the presence of proplanolol. For the pathologic features, SHR is more prone to vasodilation by propofol. This might be the reason why there were no differences in bloodpressure between SHR and WKY.
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