PASTIC Dspace Repository

Quercetin inhibits human sperm functions by reducing sperm [Ca2+]i and tyrosine phosphorylation

Show simple item record

dc.contributor.author Liang, Xiaolei
dc.contributor.author Xia, Zhili
dc.contributor.author Yan, Jiexi
dc.contributor.author Wang, Yiqing
dc.contributor.author Xue, Shilong
dc.contributor.author Zhang, Xuehong
dc.date.accessioned 2022-10-18T10:29:22Z
dc.date.available 2022-10-18T10:29:22Z
dc.date.issued 2016-11-16
dc.identifier.issn 1011-601X
dc.identifier.uri http://142.54.178.187:9060/xmlui/handle/123456789/13205
dc.description.abstract Quercetin is widely known as potent natural antioxidant and scavenger of reactive oxygen species (ROS) and nitric oxide both in vitro and in vivo. Quercetin has a wide range of biological functions and health-promoting effects. There are more and more interests in the addition of this flavonol to various traditional food products. However, the in vitro toxicity of quercetin to mature human sperm remains unknown. In this study, we investigated the in vitro effects of quercetin on human sperm functions. The results showed that the total sperm motility were significantly inhibited compared to the controls following exposure to 100, 200 and 400µM quercetin for 6 and 12h; quercetin did not affect human sperm viability. The acrosome reaction and capacitation induced by progesterone were dose-dependently inhibited by quercetin. Furthermore, quercetin induced a significantly decrease of human sperm [Ca2+]i after 2 min above 50 µM, and dose-dependently decreased the protein-tyrosine phosphorylation of human sperm. Our results indicated that quercetin may decrease sperm [Ca2+]i, suppresse tyrosine phosphorylation, and subsequently inhibit sperm functions. en_US
dc.language.iso en en_US
dc.publisher Karachi: Faculty of Pharmacy & Pharmaceutical Sciecnes, University of Karachi en_US
dc.subject Quercetin en_US
dc.subject sperm en_US
dc.subject [Ca2+]i en_US
dc.subject tyrosine phosphorylation en_US
dc.title Quercetin inhibits human sperm functions by reducing sperm [Ca2+]i and tyrosine phosphorylation en_US
dc.type Article en_US


Files in this item

This item appears in the following Collection(s)

Show simple item record

Search DSpace


Advanced Search

Browse

My Account