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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Orawan Wongmekiat | en_US |
dc.contributor.author | Kamthorn Thamprasert | en_US |
dc.contributor.author | Dusit Lumlertgul | en_US |
dc.date.accessioned | 2018-09-10T04:00:56Z | - |
dc.date.available | 2018-09-10T04:00:56Z | - |
dc.date.issued | 2007-08-01 | en_US |
dc.identifier.issn | 14401681 | en_US |
dc.identifier.issn | 03051870 | en_US |
dc.identifier.other | 2-s2.0-34347342682 | en_US |
dc.identifier.other | 10.1111/j.1440-1681.2007.04651.x | en_US |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=34347342682&origin=inward | en_US |
dc.identifier.uri | http://cmuir.cmu.ac.th/jspui/handle/6653943832/60894 | - |
dc.description.abstract | 1. Although α-tocopherol has been shown to improve renal function following ischaemia-reperfusion (I/R) injury, its clinical use is not common because α-tocopherol requires several days of pretreatment to exhibit anti-oxidative benefits. The advent of trolox, a water-soluble analogue of α-tocopherol, has raised the possibility that this compound may function more rapidly during acute oxidative stress than the conventional α-tocopherol. 2. The present study was undertaken to determine the effects of the short-term administration of trolox on renal excretory function following I/R in rats. 3. Male Wistar rats were subjected to 45 min unilateral renal artery occlusion followed by 120 min reperfusion. The control I/R group was subjected to I/R and received saline as an intravenous bolus (2 mL/kg) followed by a continuous infusion of 2 mL/kg per h starting 30 min before ischaemia, whereas the three trolox-treated I/R groups were given an i.v. bolus of trolox (2.5 mg/kg) followed by a continuous infusion (12 mg/kg per h) starting at 30 min before ischaemia, 5 min before reperfusion and 5 min after reperfusion, respectively. Renal function, malondialdehyde, glutathione and histopathology were evaluated. 4. Ischaemia-reperfusion produced a significant deterioration of renal function, which was accompanied by an elevated malondialdehyde and depleted glutathione content. Kidneys from control I/R rats demonstrated tubular cell transformation, brush border loss, vacuolation, cast formation and tubular obstruction. These changes were attenuated by trolox treatment, with the best improvement achieved when trolox was delivered 5 min before reperfusion. 5. The results demonstrate the renoprotective effects of the short-term administration of trolox on I/R injury. These findings indicate the ability of trolox to overcome a major drawback of using α-tocopherol and suggest that trolox may offer a therapeutic advantage over α-tocopherol in acute ischaemic renal failure settings. © 2007 The Authors. | en_US |
dc.subject | Biochemistry, Genetics and Molecular Biology | en_US |
dc.subject | Medicine | en_US |
dc.subject | Pharmacology, Toxicology and Pharmaceutics | en_US |
dc.title | Renoprotective effect of trolox against ischaemia-reperfusion injury in rats | en_US |
dc.type | Journal | en_US |
article.title.sourcetitle | Clinical and Experimental Pharmacology and Physiology | en_US |
article.volume | 34 | en_US |
article.stream.affiliations | Chiang Mai University | en_US |
Appears in Collections: | CMUL: Journal Articles |
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