Sharif Khozein, M. Eslami, Farhad Farrokhi-Ardabili
{"title":"Improvement of ram semen quality by luteolin enrichment during cold preservation","authors":"Sharif Khozein, M. Eslami, Farhad Farrokhi-Ardabili","doi":"10.5194/aab-67-123-2024","DOIUrl":null,"url":null,"abstract":"Abstract. The present experiment aimed to investigate the probable protective role of luteolin (Lut) in ram spermatozoa kinematics and the oxidative/anti-oxidative/nitrosative status of semen during cold storage. Ejaculates were collected from five Qezel rams twice a week. Ejaculates were pooled, diluted with Tris–egg yolk extender (negative control) or supplemented with 0 (control; received the solvent of luteolin), 4, 8 and 16 µm Lut. Kinematics parameters, viability and membrane functionality of spermatozoa were assessed. Furthermore, amounts of malondialdehyde (MDA) and anti-oxidant activity (AOA), superoxide dismutase activity (SOD) and total nitrate nitrite (TNN) were evaluated in the medium (diluent) and spermatozoa, separately, at 0, 24, 48 and 72 h after storage at 4 °C. Percentages of forward progressive motility and membrane integrity were significantly higher in 8 and 16 µm groups compared to control groups at 72 h (P<0.05). No significant differences were observed in viability among groups during the study (P>0.05). Lower MDA contents were observed in medium and spermatozoa of 8 and 16 µm treated groups compared to controls at 72 h (P<0.05). In addition, higher AOA levels were observed in the medium of Lut-treated groups compared to controls at 48 and 72 h (P<0.05). The activity of SOD was improved by luteolin addition. Luteolin enrichment did not affect TNN amounts. It seems that luteolin (at 8 and 16 µm) as a flavonoid protects the ram semen by its anti-oxidative properties and by reduction of lipid peroxidation following 48 and 72 h storage.\n","PeriodicalId":502344,"journal":{"name":"Archives Animal Breeding","volume":"38 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Archives Animal Breeding","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5194/aab-67-123-2024","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Abstract. The present experiment aimed to investigate the probable protective role of luteolin (Lut) in ram spermatozoa kinematics and the oxidative/anti-oxidative/nitrosative status of semen during cold storage. Ejaculates were collected from five Qezel rams twice a week. Ejaculates were pooled, diluted with Tris–egg yolk extender (negative control) or supplemented with 0 (control; received the solvent of luteolin), 4, 8 and 16 µm Lut. Kinematics parameters, viability and membrane functionality of spermatozoa were assessed. Furthermore, amounts of malondialdehyde (MDA) and anti-oxidant activity (AOA), superoxide dismutase activity (SOD) and total nitrate nitrite (TNN) were evaluated in the medium (diluent) and spermatozoa, separately, at 0, 24, 48 and 72 h after storage at 4 °C. Percentages of forward progressive motility and membrane integrity were significantly higher in 8 and 16 µm groups compared to control groups at 72 h (P<0.05). No significant differences were observed in viability among groups during the study (P>0.05). Lower MDA contents were observed in medium and spermatozoa of 8 and 16 µm treated groups compared to controls at 72 h (P<0.05). In addition, higher AOA levels were observed in the medium of Lut-treated groups compared to controls at 48 and 72 h (P<0.05). The activity of SOD was improved by luteolin addition. Luteolin enrichment did not affect TNN amounts. It seems that luteolin (at 8 and 16 µm) as a flavonoid protects the ram semen by its anti-oxidative properties and by reduction of lipid peroxidation following 48 and 72 h storage.