Abstract | AIM: METHODS: The cecum was ligated and punctured in rats under anesthesia. CPU0213 (30 mg .kg(-1).d(-1), bid, sc X 3 d) was administered 8 h after surgical operation. RESULTS: In the untreated septic shock group, the mean arterial pressure and survival rate were markedly decreased (P<0.01), and heart rate, weight index of kidney, serum creatinine and blood urea nitrogen, 24 h urinary protein and creatinine were significantly increased (P<0.01). The levels of ET-1, total NO synthetase (tNOS), indusible nitric oxide synthetase (iNOS), nitric oxide (NO), and ROS in serum and the renal cortex were markedly increased (P<0.01). The upregulation of the mRNA levels of preproET-1, endothelin converting enzyme, ET(A), ET(B), iNOS, and tumor necrosis factor-alpha in the renal cortex was significant (P<0.01). The protein amount of activated NF-kappaB was significantly increased (P<0.01) in comparison with the sham operation group. All of these changes were significantly reversed after CPU0213 administration. CONCLUSION: Upregulation of the ET signaling pathway and NF-kappaB play an important role in the ARF of septic shock. Amelioration of renal lesions was achieved by suppressing the ET(A) and ET(B) receptors in the renal cortex following CPU0213 medication.
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Authors | Hai-bo He, De-zai Dai, Yin Dai |
Journal | Acta pharmacologica Sinica
(Acta Pharmacol Sin)
Vol. 27
Issue 9
Pg. 1213-21
(Sep 2006)
ISSN: 1671-4083 [Print] United States |
PMID | 16923343
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- CPU0213
- Endothelin Receptor Antagonists
- Endothelin-1
- NF-kappa B
- Pyrazoles
- RNA, Messenger
- Reactive Oxygen Species
- Tumor Necrosis Factor-alpha
- Nitric Oxide
- Nitric Oxide Synthase
- Nitric Oxide Synthase Type II
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Topics |
- Acute Kidney Injury
(blood, etiology, metabolism)
- Animals
- Endothelin Receptor Antagonists
- Endothelin-1
(biosynthesis, genetics)
- Kidney Cortex
(metabolism)
- Male
- NF-kappa B
(metabolism)
- Nitric Oxide
(blood, metabolism)
- Nitric Oxide Synthase
(blood, metabolism)
- Nitric Oxide Synthase Type II
(blood, metabolism)
- Pyrazoles
(pharmacology)
- RNA, Messenger
(biosynthesis, genetics)
- Rats
- Rats, Wistar
- Reactive Oxygen Species
(blood, metabolism)
- Shock, Septic
(blood, complications, metabolism)
- Tumor Necrosis Factor-alpha
(biosynthesis, genetics)
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