Renoprotective effect of trolox against ischaemia-reperfusion injury in rats
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...
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th-cmuir.6653943832-608942018-09-10T04:09:36Z Renoprotective effect of trolox against ischaemia-reperfusion injury in rats Orawan Wongmekiat Kamthorn Thamprasert Dusit Lumlertgul Biochemistry, Genetics and Molecular Biology Medicine Pharmacology, Toxicology and Pharmaceutics 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. 2018-09-10T04:00:56Z 2018-09-10T04:00:56Z 2007-08-01 Journal 14401681 03051870 2-s2.0-34347342682 10.1111/j.1440-1681.2007.04651.x https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=34347342682&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/60894 |
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Biochemistry, Genetics and Molecular Biology Medicine Pharmacology, Toxicology and Pharmaceutics Orawan Wongmekiat Kamthorn Thamprasert Dusit Lumlertgul Renoprotective effect of trolox against ischaemia-reperfusion injury in rats |
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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. |
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Journal |
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Orawan Wongmekiat Kamthorn Thamprasert Dusit Lumlertgul |
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Orawan Wongmekiat Kamthorn Thamprasert Dusit Lumlertgul |
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Orawan Wongmekiat |
title |
Renoprotective effect of trolox against ischaemia-reperfusion injury in rats |
title_short |
Renoprotective effect of trolox against ischaemia-reperfusion injury in rats |
title_full |
Renoprotective effect of trolox against ischaemia-reperfusion injury in rats |
title_fullStr |
Renoprotective effect of trolox against ischaemia-reperfusion injury in rats |
title_full_unstemmed |
Renoprotective effect of trolox against ischaemia-reperfusion injury in rats |
title_sort |
renoprotective effect of trolox against ischaemia-reperfusion injury in rats |
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2018 |
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https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=34347342682&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/60894 |
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