| Project/Area Number |
21890212
|
|---|
| Research Category |
Grant-in-Aid for Research Activity Start-up
|
| Allocation Type | Single-year Grants |
|---|
| Research Field |
Kidney internal medicine
|
|---|
| Research Institution | Yokohama City University |
|---|
Principal Investigator |
MITSUHASHI Hiroshi Yokohama City University, 医学部, 助教 (90517020)
|
|---|
| Co-Investigator(Renkei-kenkyūsha) |
TAMURA Kouichi 横浜市立大学, 医学部, 准教授 (40285143)
|
|---|
| Project Period (FY) |
2009 – 2010
|
| Project Status |
Completed (Fiscal Year 2010)
|
| Budget Amount *help |
¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Fiscal Year 2010: ¥988,000 (Direct Cost: ¥760,000、Indirect Cost: ¥228,000)
Fiscal Year 2009: ¥1,092,000 (Direct Cost: ¥840,000、Indirect Cost: ¥252,000)
|
|---|
| Keywords | 高血圧学 / 受容体 / 腎障害 / 生体分子 / 高血圧 / トランスレーショナルリサーチ |
|---|
| Research Abstract |
Dahl salt-sensitive hypertensive rats (DS rats, 3 wks of age) were divided into three groups for oral administration of vehicle (vehicle group) or ARB either continuously from 6 to 16 wks of age (continuous ARB group) or transiently from 3 to 10 wks of age (transient ARB group) and fed high salt diet from 6 to 16 wks of age. DS rats fed a normal salt diet were used as controls (control group). Not only continuous ARB treatment (SBP 149±9 mmHg) but also transient ARB treatment (SBP 142±7 mmHg) significantly improved hypertension at 16 wks of age with reduction of urinary protein excretion, as compared to vehicle group (SBP 199±15 mmHg). With respect to the regulation of ATRAP expression in the kidney, the renal ATRAP expression was significantly suppressed in vehicle group compared with control group. However, transient ARB treatment as well as continuous ARB treatment significantly recovered the suppressed renal ATRAP expression. These results indicate that the transiently administrated ARB-mediated sustained activation of renal ATRAP expression may play a role in the long-term therapeutic effects of ARB even after withdrawal on hypertension and renal injury in salt-induced hypertension.
|
