Abstract | BACKGROUND: METHODS: This study was performed on male Sprague-Dawley rats with liver cirrhosis induced by common bile duct ligation. They received subcutaneous indomethacin (5 mg/kg/day) or distilled water (control) injection from the 36th to 42nd day after operation. On the 43rd day, systemic and portal hemodynamics were evaluated and the following experiments were performed with an in situ collateral perfusion model: in the first series, concentration-response curves to AVP (10(-10) to 10(-7) M) were obtained; in the second series, flow-pressure curves were plotted ( Krebs solution, 6-18 mL/min), where the slope represents an index of collateral vascular resistance (the higher the resistance, the smaller the amount of shunting vessels, that is, the lower the degree of shunting). RESULTS: The mean arterial pressure and portal pressure were similar between indomethacin and control groups (p > 0.05). Indomethacin elevated the collateral perfusion pressure to AVP (3 x 10(-9), 10(-8) M, p < 0.05) but did not influence the slope of the flow-pressure curve (p > 0.05). CONCLUSION: In bile duct-ligated cirrhotic rats, indomethacin improves the portal-systemic collateral vascular responsiveness to AVP without alleviating the severity of shunting.
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Authors | Hui-Chun Huang, Sun-Sang Wang, Ching-Chih Chang, Fa-Yauh Lee, Full-Young Chang, Han-Chieh Lin, Ming-Chih Hou, Rei-Hwa Lu, Shou-Dong Lee |
Journal | Journal of the Chinese Medical Association : JCMA
(J Chin Med Assoc)
Vol. 70
Issue 12
Pg. 521-6
(Dec 2007)
ISSN: 1726-4901 [Print] Netherlands |
PMID | 18194892
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Arginine Vasopressin
- Indomethacin
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Topics |
- Animals
- Arginine Vasopressin
(pharmacology)
- Bile Ducts
- Blood Pressure
(drug effects)
- Collateral Circulation
(drug effects)
- Dose-Response Relationship, Drug
- Indomethacin
(therapeutic use)
- Ligation
- Liver Cirrhosis, Experimental
(drug therapy, physiopathology)
- Male
- Rats
- Rats, Sprague-Dawley
- Vascular Resistance
(drug effects)
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