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Antioxidant, antimicrobial activity and inhibition of α-glucosidase activity by Betula alnoides Buch. bark extract and their relationship with polyphenolic compounds concentration.
Immunopharmacol Immunotoxicol. 2012 Oct; 34(5):824-31.II

Abstract

Betula alnoides has been widely used in local traditional medicinal treatment for a variety of diseases, wounds and to cure diabetes. The air-dried, powdered (200 g) bark was extracted with 80% methanol at room temperature. The combined 80% methanolic extract was partitioned with organic solvents to yield n-hexane, ethyl acetate (EtOAc), n-butanol (BuOH; water saturated), and aqueous fractions for the investigation of antioxidant and antimicrobiology and α-glucosidase activity effects (GAE) of B. alnoides. Antioxidant activity was studied by using antioxidant tests, including electron donation ability test, reducing power, and metal-chelating activity assay. Antioxidant, antimicrobial activity and α-glucosidase inhibitory effect of 80% methanolic extracts and fractions derived from the bark of B. alnoides were evaluated and determined. The results showed that 80% methanolic extracts exhibited high 1,1-diphenyl-2-picrylhydrazyl (DPPH) scavenging activity (80.68%). In addition, both the 80% methanolic extract and EtOAc fraction exhibited more potent reducing activity than did butylated hydroxyanisole (BHA) and trolox. The aqueous fraction had higher metal-chelating activity than other fractions. The EtOAc fraction had the highest phenolic and flavonoid content (217.73 ± 1.02 mg GAE/g extract, and 38.42 ± 1.87 mg QE/g extract, respectively). The 80% methanolic extract and EtOAc fraction showed higher levels of antimicrobial activity than did other fractions. The 80% methanolic extract had the most powerful α-glucosidase inhibitory effect (98.46%) at a concentration of 40 µg/mL. The results suggest that bark extracts of B. alnoides could be a potential source of natural antioxidants and for treating pathogenic diseases.

Authors+Show Affiliations

Department of Ethnobotany and Social Medicine, Sikkim University, Gangtok, India.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

22380707

Citation

Ghimire, Bimal Kumar, et al. "Antioxidant, Antimicrobial Activity and Inhibition of Α-glucosidase Activity By Betula Alnoides Buch. Bark Extract and Their Relationship With Polyphenolic Compounds Concentration." Immunopharmacology and Immunotoxicology, vol. 34, no. 5, 2012, pp. 824-31.
Ghimire BK, Tamang JP, Yu CY, et al. Antioxidant, antimicrobial activity and inhibition of α-glucosidase activity by Betula alnoides Buch. bark extract and their relationship with polyphenolic compounds concentration. Immunopharmacol Immunotoxicol. 2012;34(5):824-31.
Ghimire, B. K., Tamang, J. P., Yu, C. Y., Jung, S. J., & Chung, I. M. (2012). Antioxidant, antimicrobial activity and inhibition of α-glucosidase activity by Betula alnoides Buch. bark extract and their relationship with polyphenolic compounds concentration. Immunopharmacology and Immunotoxicology, 34(5), 824-31. https://doi.org/10.3109/08923973.2012.661739
Ghimire BK, et al. Antioxidant, Antimicrobial Activity and Inhibition of Α-glucosidase Activity By Betula Alnoides Buch. Bark Extract and Their Relationship With Polyphenolic Compounds Concentration. Immunopharmacol Immunotoxicol. 2012;34(5):824-31. PubMed PMID: 22380707.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Antioxidant, antimicrobial activity and inhibition of α-glucosidase activity by Betula alnoides Buch. bark extract and their relationship with polyphenolic compounds concentration. AU - Ghimire,Bimal Kumar, AU - Tamang,Jyoti Prakash, AU - Yu,Chang Yeon, AU - Jung,Suk Jun, AU - Chung,Ill Min, Y1 - 2012/03/02/ PY - 2012/3/3/entrez PY - 2012/3/3/pubmed PY - 2013/2/5/medline SP - 824 EP - 31 JF - Immunopharmacology and immunotoxicology JO - Immunopharmacol Immunotoxicol VL - 34 IS - 5 N2 - Betula alnoides has been widely used in local traditional medicinal treatment for a variety of diseases, wounds and to cure diabetes. The air-dried, powdered (200 g) bark was extracted with 80% methanol at room temperature. The combined 80% methanolic extract was partitioned with organic solvents to yield n-hexane, ethyl acetate (EtOAc), n-butanol (BuOH; water saturated), and aqueous fractions for the investigation of antioxidant and antimicrobiology and α-glucosidase activity effects (GAE) of B. alnoides. Antioxidant activity was studied by using antioxidant tests, including electron donation ability test, reducing power, and metal-chelating activity assay. Antioxidant, antimicrobial activity and α-glucosidase inhibitory effect of 80% methanolic extracts and fractions derived from the bark of B. alnoides were evaluated and determined. The results showed that 80% methanolic extracts exhibited high 1,1-diphenyl-2-picrylhydrazyl (DPPH) scavenging activity (80.68%). In addition, both the 80% methanolic extract and EtOAc fraction exhibited more potent reducing activity than did butylated hydroxyanisole (BHA) and trolox. The aqueous fraction had higher metal-chelating activity than other fractions. The EtOAc fraction had the highest phenolic and flavonoid content (217.73 ± 1.02 mg GAE/g extract, and 38.42 ± 1.87 mg QE/g extract, respectively). The 80% methanolic extract and EtOAc fraction showed higher levels of antimicrobial activity than did other fractions. The 80% methanolic extract had the most powerful α-glucosidase inhibitory effect (98.46%) at a concentration of 40 µg/mL. The results suggest that bark extracts of B. alnoides could be a potential source of natural antioxidants and for treating pathogenic diseases. SN - 1532-2513 UR - https://www.unboundmedicine.com/medline/citation/22380707/Antioxidant_antimicrobial_activity_and_inhibition_of_α_glucosidase_activity_by_Betula_alnoides_Buch__bark_extract_and_their_relationship_with_polyphenolic_compounds_concentration_ L2 - https://www.tandfonline.com/doi/full/10.3109/08923973.2012.661739 DB - PRIME DP - Unbound Medicine ER -