• 제목/요약/키워드: Bovine Lens Aldose Reductase

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Effects of Some Monoterpenes on Bovine Lens Aldose Reductase Activity

  • Moon, Chang-Kiu;Choi, Soo-Young;Ha, Bae-Jin
    • Archives of Pharmacal Research
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    • 제11권4호
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    • pp.312-314
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    • 1988
  • Thirteen monoterpenes were examined for their effects on the bovine lens aldose reductase activity. the monoterpenes tested in this study showed mild inhibitory effects except 3-carene which did not show any significant effect. At the concentration of $10^{-3}$ M(+) Pulegon showed 42% inhibition on lens aldose reductase activity, which is the most otent effect among the tested substance.

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Bovine lens aldose reductase inhibitory effects of some natural monoterpense

  • Moon, Chang-Kiu;Yun, Yeo-Pyo;Lim, Jong-Seok;Ryu, Chung-Kye
    • Archives of Pharmacal Research
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    • 제8권4호
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    • pp.273-275
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    • 1985
  • Carvomethone, (+) pulegone, (-)isopulegol and (-) menthone, which are natural and widely distributed in the plantkingdom, were examined for their Lens Aldose Reductase inhibitory effects. All monoterpenes tested showed that the mild inhibitory effects. Inhibition percents of four monoterpenes were in the range of 23-42% at $10^{-3}M$ and 5-21% at $10^{-4}M$.

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수종 생약에 의한 Lens Aldose Reductase의 억제 (Inhibition of Lens Aldose Reductase by Medicinal Plants)

  • 정도래;박웅양;이승호;이경순;노재섭
    • 생약학회지
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    • 제24권1호
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    • pp.58-62
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    • 1993
  • To search for inhibitory activities for lens aldose reductase, twenty two medicinal plants were tested by the method of bovine lens aldose reductase inhibition test. In this test Rubia akane(68%), Artemisia selengensis(61%), Lespedeza cuneata (58%), Ligustrum lucidum(58%), Viola patrinii(58%) extracts were shown to have aldose reductase inhibitory activity. From the radix of Rubia akane, $2-methyl-1,\;3,\;6-trihydroxy-9,\;10-anthraquinone-3-O-(6'-O-acetyl)-{\alpha}-rhamnosyl-(1{\rightarrow}2)-{\beta}-D-glucoside$ was isolated and the $IC_{50}$ of this compound in the aldose reductase inhibition test was about $1.2{\times}10^{-6}M$.

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Effects of Some Coumarin Derivatives on the Bovine Lens Aldose Reductase Activity

  • Moon, Chang-Kiu;Lee, Se-Chang;Yun, Yeo-Pyo;Ha, Bae-Jin;Yook, Chang-Soo
    • Archives of Pharmacal Research
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    • 제11권4호
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    • pp.308-311
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    • 1988
  • Nine coumarin dervatives were examined for thier inhibitory effects on bovine lens aldose reductase activity (bovine-LAR). More than 50% inhibition of BLAR activities was observed in the cases of treatments with decursin, decursinol, esculin, isoimperatorin, oxypeucedanine and isobergapten at the concentration of $10^{-4}$M. Especially, BLAR activity was completely inhibited by the treatment of decursin and decursinol at this concentration. At $10^{-5}$ M, only three coumarins-decursin, decursinol and isoimperatorin, were found to have still relatively higher inhibitory effect.

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꾸지뽕나무 근피의 항당뇨병 효과 (Hypoglycemic Effect of Cudrania tricuspidata Root Bark)

  • 박웅양;노재섭;이경순
    • 생약학회지
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    • 제32권3호통권126호
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    • pp.248-252
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    • 2001
  • The present study was undertaken to elucidate the hypoglycemic effect and inhibitory effect of Cudrania tricuspidata root bark on aldose reductase activity. C. tricuspidata MeOH ext. 1,000 mg/kg showed a significant blood glucose lowering effect on alloxan-induced hyperglycemic rats and increasing body weight. C. tricuspidata MeOH ext. showed a potent inhibitory effect on bovine lens aldose reductase.

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Effects of Furanocoumarins from Angelica Dahurica on Aldose Reductase and Galactosemic Cataract Formation in Rats

  • Shin, Kuk-Hyun;Chung, Myung-Sook;Cho, Tae-Soon
    • Archives of Pharmacal Research
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    • 제17권5호
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    • pp.331-336
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    • 1994
  • The ether extract from the roots of angelica clahurica was found to inhibit bovine lens aldose reductase (BLAR0 activity in vitro by 100% at 100.mu.g/ml. Systematic fractionation of the ether soluble fraction and subsequent active frctions monitorede by bioassy led to isolation of four furanocoumarins, isoimperatorin (I0, imperatorin (II), ter-O-methyl byakangelicin (III) and byakangelicin (IV), among which compound III and IV were identified as potential AR inhibitors, their $IC_{50}$ values being $2.8{\mu}M{\;}and{\;}6.2{\mu}M$, respectively. Galactosemic cataract formation tors, in rats treated with 40 g/kg/day of galactose was blocked almost completely throughout the exeprimental periods up to 44 days by i.p. administrations of byakangelicin (IV) at 50 mg/kg/day. In coincidence with the inhibitory action on cataract formation, the galactitol accumulation in rats treated with byakangelicin (IV) was found to be markedly prevented by approximately 80.5% compared to those of the contro. These results indicate that byakangelicin (IV), as a main principle of this plant, possesses high potential for a clinically useful drug of the future which prevents and/or improves sugar cataract as well as diabetic complications.

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Effect of Byakangelicin from Angelica dahurica and its Semi-synthetic Derivatives on Aldose Reductase, Galactosemic Cataracts, the Polyol Contents and $Na^{+}$, $K^{+}$-ATPase activity in Sciatic Nerves of Streptozotocin-induced Diabetic Rats.

  • Lim, Soon-Sung;Jung, Sang-Hoon;Shin, Kuk-Hyun
    • 한국응용약물학회:학술대회논문집
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    • 한국응용약물학회 1998년도 Proceedings of UNESCO-internetwork Cooperative Regional Seminar and Workshop on Bioassay Guided Isolation of Bioactive Substances from Natural Products and Microbial Products
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    • pp.184-184
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    • 1998
  • Aldose reductase(AR), a rate-limiting enzyme in the polyol pathway, has been demonstrated to cause the intracellular accumulation of sorbitol or galactitol and hence to play key roles not only in the cataract formation in the lens but also in the pathogenesis of diabetic complications such as neuropathy, retinopathy and nephropathy, etc. In a series of investigations to evaluate potential AR inhibitors from medicinal plants, we have shown that some hot water extracts exhibited a significant inhibition of a significant inhibition of bovine lens AR in vitro. Among active plants, the roots of Angelica dahuria (Umbelliferae) were shown to have relatively potent AR inhibitory activity. Systematic fractionation of the ether soluble fraction monitored by bioassay led to isolation of two furanocoumarins, byakangelicin(I) and ter-O-methyl byakangelicin( II), were identified as potential AR inhibitors, their $IC_{50}$ values being 6.2 M and 2.8 M, respectively.

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