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A phenolic antioxidant from the freshwater orchid,Habenaria repens
Institution:1. Biotechnology and Biodiversity Group, Department of Applied Chemistry and Production Systems, Chemical Sciences Faculty, Universidad de Cuenca, Av. 12 de Abril s/n, Cuenca, Ecuador;1. Department of Biochemistry, Genetics and Microbiology, Forestry and Agricultural Biotechnology Institute (FABI), University of Pretoria, South Africa;2. Department of Zoology and Entomology, Forestry and Agricultural Biotechnology Institute (FABI), University of Pretoria, South Africa;3. Institute for Dehesa Research (INDEHESA). Universidad de Extremadura, Plasencia, Spain;4. Private Bag XC4, Postlink Suite 38, Woodhill, Pretoria 0083, South Africa;1. Biotechnology Division, Council of Scientific and Industrial Research-Institute of Himalayan Bioresource Technology, P.O. Box 6, Palampur, HP 176061, India;2. Agrotechnology and Rural Development Division (ARDD), CSIR-North East Institute of Science & Technology, Jorhat 785006, Assam, India;3. Chemical Technology Division, CSIR-Institute of Himalayan Bioresource Technology, Palampur, Himachal Pradesh 176061, India;4. Academy of Scientific and Innovative Research (AcSIR), Ghaziabad 201002, India
Abstract:Recently, an unusual compound named habenariol was isolated from the freshwater orchid, Habenaria repens. Its phenolic structure suggested that habenariol should have substantial antioxidant activity. This possibility was investigated by evaluating the capacity of habenariol to inhibit copper-induced lipid peroxidation of human low density lipoprotein (LDL), a popular experimental model. LDL was incubated with 5 μM cupric chloride in the presence and absence of habenariol or a positive control, viz., α-tocopherol. Both kinetic and end-point spectrophotometric assays were used to determine extent of lipid peroxidation of LDL. In the kinetic assay, the time elapsing before the onset of rapid formation of conjugated lipid hydroperoxides in LDL (marked by a sharp increase in UV absorbance) was prolonged by habenariol, indicative of an antioxidant effect. In the end-point assay, direct colorimetric measurement confirmed habenariol's ability to inhibit formation of lipid hydroperoxides. However, in both assays, habenariol was less potent than α-tocopherol in inhibiting lipid peroxidation of LDL.
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