Roles of PPARγ agonists in regulation of body-fluid volume and blood pressure
| Project/Area Number |
16590779
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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 |
Kidney internal medicine
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| Research Institution | The University of Tokyo |
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Principal Investigator |
SEKI George The University of Tokyo, Faculty of Medicine, Lecturer, 医学部附属病院, 講師 (30206619)
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| Co-Investigator(Kenkyū-buntansha) |
NOIRI Eisei The University of Tokyo, Faculty of Medicine, Lecturer, 医学部附属病院, 講師 (00301820)
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| Project Period (FY) |
2004 – 2005
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| Project Status |
Completed (Fiscal Year 2005)
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| Budget Amount *help |
¥3,600,000 (Direct Cost: ¥3,600,000)
Fiscal Year 2005: ¥1,000,000 (Direct Cost: ¥1,000,000)
Fiscal Year 2004: ¥2,600,000 (Direct Cost: ¥2,600,000)
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| Keywords | Thiazolidinediones / Edema / ERK / PPARγ / 近位尿細管 |
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| Research Abstract |
Thiazolidinediones (TZD) are anti-diabetic drugs, which improve insulin-resistance. Although they are quite effective in treating diabetics, TZD have serious side effects of Na-retention. To clarify the mechanism of Na-retention by TZD, we examined the effects of TZD of renal proximal functions. In isolated proximal tubules from rabbit, TZD markedly activated NBC1 activity, and enhanced the rate of HCO3 absorption within several minutes. These results were blocked by MEK inhibitor as well as by PPARγ antagonist. TZD also enhanced ERK phosphorylation in renal cortex.
In fibroblast cells from wild-type mice, TZD enhanced the activity of NHE1. This effect was also blocked by MEK inhibitor as well as by PPARγ antagonist. In fibroblast cells from PPARγ-KO mice, however, TZD enhanced the NHE1 activity only after adenovirus-mediated PPARγ gene transfer. When only the ligand-binding domain was introduced in KO cells, however, TZD did not activate the NHE1. These results indicate that TZD stimulates renal proximal absorption through PPARγ/ERK pathway.
We also showed that insulin stimulates renal proximal absorption via PI3-kinase. In addition, IRS-2, but not IRS-1, plays an essential role in insulin effects of proximal function. Since defects in IRS-1 are frequently reported in type 2 diabetics or obesity, IRS-1 independent stimulation of renal Na-retention may have an important role in pathogenesis of hypertension associated with insulin-resistance.
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Report
(3 results)
Research Products
(8 results)
