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Please use this identifier to cite or link to this item:
http://krishi.icar.gov.in/jspui/handle/123456789/54223
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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Selvaraju S | en_US |
dc.contributor.author | Siva Subramani T | en_US |
dc.contributor.author | Raghavendra BS | en_US |
dc.contributor.author | Ravindra JP | en_US |
dc.date.accessioned | 2021-08-10T09:19:18Z | - |
dc.date.available | 2021-08-10T09:19:18Z | - |
dc.date.issued | 2010-12-01 | - |
dc.identifier.citation | Selvaraju S, Siva Subramani T, Raghavendra BS and Ravindra JP. 2010. Effect of IGF-I on spermatozoa membrane protein profile and correlation between seminal plasma IGF-I and antioxidant enzymes in buffalo semen. Indian Journal of Animal Science, 80:1171-74. | en_US |
dc.identifier.issn | Not Available | - |
dc.identifier.uri | http://krishi.icar.gov.in/jspui/handle/123456789/54223 | - |
dc.description | Not Available | en_US |
dc.description.abstract | The present study assessed the effect of insulin like growth factor–I (IGF-I) on spermatozoa membrane protein profile and relationship between IGF-I and antioxidant levels in buffalo (Bubalus bubalis) semen. Immediately after semen collection (n = 8), the seminal plasma and spermatozoa cells were separated by centrifugation (5000 g/10 min) and the seminal plasma IGF-I and antioxidant enzymes estimations were carried out. The spermatozoa were diluted (20 million cells/ml) in a tris-egg yolk extender, IGF-I (100 ng/ml of the semen) was added and incubated at 37ºC for 2 h. Membrane proteins were extracted with 0.1% Triton X 100 and protein profile was carried out by denaturing gel electrophoresis. No change in membrane protein profile was observed in spermatozoa treated with IGF-I as compared to control. The mean buffalo seminal plasma IGF-I, superoxide dismutase (SOD) and glutathione peroxidise (GPx) concentrations were 139.07±23.61 ng/ml (range: 51.45 to 267.43), 0.38±0.03 Unit/mg of protein (range: 0.16 to 0.74) and was 168.15±35.54 IU/mg of protein (range: 77 to 401), respectively while the total protein concentration (G %) was 2.89±0.20 (range: 0.88 to 5.27). IGF-I had no significant, correlation with SOD (r = –0.17) and GPx (r = –0.38). The correlation between SOD and GPx was significant and positive (r = 0.77). The present study revealed that IGF-I had no correlation with SOD and GPx levels and its addition did not influence spermatozoa membrane protein profile in a spermatozoa incubated for 2 h | en_US |
dc.description.sponsorship | Not Available | en_US |
dc.language.iso | English | en_US |
dc.publisher | ICAR | en_US |
dc.relation.ispartofseries | Not Available; | - |
dc.subject | Buffalo | en_US |
dc.subject | GPx | en_US |
dc.subject | IGF-I | en_US |
dc.subject | SOD | en_US |
dc.subject | Spermatozoa membrane protein | en_US |
dc.title | Effect of IGF-I on spermatozoa membrane protein profile and correlation between seminal plasma IGF-I and antioxidant enzymes in buffalo semen | en_US |
dc.title.alternative | Not Available | en_US |
dc.type | Journal | en_US |
dc.publication.projectcode | Not Available | en_US |
dc.publication.journalname | Indian Journal of Animal Sciences | en_US |
dc.publication.volumeno | 80(12) | en_US |
dc.publication.pagenumber | 1171-74 | en_US |
dc.publication.divisionUnit | Animal Physiology division | en_US |
dc.publication.sourceUrl | http://epubs.icar.org.in/ejournal/index.php/IJAnS/article/view/2200/531 | en_US |
dc.publication.authorAffiliation | ICAR::National Institute of Animal Nutrition and Physiology | en_US |
dc.ICARdataUseLicence | http://krishi.icar.gov.in/PDF/ICAR_Data_Use_Licence.pdf | en_US |
dc.publication.naasrating | 6.28 | en_US |
Appears in Collections: | AS-NIANP-Publication |
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