Description
Hesperidin is a phytoestrogen and flavonoid found in citrus plants that exhibits anti-hyperlipidemic, anti-osteoporotic, anti-inflammatory, analgesic, sedative, antinociceptive, and antioxidative activities. In vivo, hesperidin increases levels of HDL and decreases levels of LDL, triglycerides, and total lipids. In ovariectomized animals, hesperidin increases bone mineral density, preventing hormone-released changes in bone volume and thickness. Hesperidin also decreases carrageenan-induced edema and displays opioid-induced pain relief in various animal models. Additionally, hesperidin inhibits COX-2 activity and scavenges radicals.
References
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Loscalzo LM, Wasowski C, Paladini AC, et al. Opioid receptors are involved in the sedative and antinociceptive effects of hesperidin as well as in its potentiation with benzodiazepines. Eur J Pharmacol. 2008 Feb 12;580(3):306-13. PMID: 18048026.
Hirata A, Murakami Y, Shoji M, et al. Kinetics of radical-scavenging activity of hesperetin and hesperidin and their inhibitory activity on COX-2 expression. Anticancer Res. 2005 Sep-Oct;25(5):3367-74. PMID: 16101151.
Chiba H, Uehara M, Wu J, et al. Hesperidin, a citrus flavonoid, inhibits bone loss and decreases serum and hepatic lipids in ovariectomized mice. J Nutr. 2003 Jun;133(6):1892-7. PMID: 12771335.
Monforte MT, Trovato A, Kirjavainen S, et al. Biological effects of hesperidin, a Citrus flavonoid. (note II): hypolipidemic activity on experimental hypercholesterolemia in rat. Farmaco. 1995 Sep;50(9):595-9. PMID: 7495469.
Emim JA, Oliveira AB, Lapa AJ. Pharmacological evaluation of the anti-inflammatory activity of a citrus bioflavonoid, hesperidin, and the isoflavonoids, duartin and claussequinone, in rats and mice. J Pharm Pharmacol. 1994 Feb;46(2):118-22. PMID: 8021799.