Expression Profile of Luteinizing Hormone Receptor Gene in Hierarchal Follicles and Regressing Oviduct Tissues of White Leghorn Hens During Moulting

Contents In the present study, the expression profile of luteinizing hormone receptor (LHR) was investigated in the ovary, magnum and uterus and in hierarchcal follicles (F‐1, F‐2, F‐3 and F‐4) of hens subjected to moulting to establish their involvement in moulting and presence in non‐gonadal tissu...

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Veröffentlicht in:Reproduction in domestic animals 2013-04, Vol.48 (2), p.278-283
Hauptverfasser: Agarwal, R, Sastry, KVH, Tripathi, V, Singh, R, Saxena, R, Mohan, J, Singh, RP
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container_end_page 283
container_issue 2
container_start_page 278
container_title Reproduction in domestic animals
container_volume 48
creator Agarwal, R
Sastry, KVH
Tripathi, V
Singh, R
Saxena, R
Mohan, J
Singh, RP
description Contents In the present study, the expression profile of luteinizing hormone receptor (LHR) was investigated in the ovary, magnum and uterus and in hierarchcal follicles (F‐1, F‐2, F‐3 and F‐4) of hens subjected to moulting to establish their involvement in moulting and presence in non‐gonadal tissues. Fifty‐two layers (72 weeks) were subjected to moult for a period of 14 days. Four birds were sacrificed each time on 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 12 and 14 days of moulting, and samples (ovary, magnum, uterus and hierarchal follicles) were collected aseptically for the quantitative study by real‐time polymerase chain reaction. The ovary, isthmus, uterus and magnum weight reduced significantly during induced moulting. From the 4 DOM, this reduction was drastic and reached approximately 80% of original weight in the case of ovary, isthmus and magnum and approximately 65% of original weight in the case of uterus on 14 DOM. Ovarian yellow follicles decreased gradually from 1 DOM to 4 DOM, after that no normal yellow follicle was observed in moulted bird. The number of atretic follicles increased gradually during the course of induced moulting, reaching the peak at 5 DOM. The LHR mRNA was detected in non‐gonadal tissues like magnum and uterus. The LHR expression was significantly (p 
doi_str_mv 10.1111/j.1439-0531.2012.02145.x
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Fifty‐two layers (72 weeks) were subjected to moult for a period of 14 days. Four birds were sacrificed each time on 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 12 and 14 days of moulting, and samples (ovary, magnum, uterus and hierarchal follicles) were collected aseptically for the quantitative study by real‐time polymerase chain reaction. The ovary, isthmus, uterus and magnum weight reduced significantly during induced moulting. From the 4 DOM, this reduction was drastic and reached approximately 80% of original weight in the case of ovary, isthmus and magnum and approximately 65% of original weight in the case of uterus on 14 DOM. Ovarian yellow follicles decreased gradually from 1 DOM to 4 DOM, after that no normal yellow follicle was observed in moulted bird. The number of atretic follicles increased gradually during the course of induced moulting, reaching the peak at 5 DOM. The LHR mRNA was detected in non‐gonadal tissues like magnum and uterus. The LHR expression was significantly (p &lt; 0.05) down regulated in ovary, magnum and uterus throughout the treatment. 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Fifty‐two layers (72 weeks) were subjected to moult for a period of 14 days. Four birds were sacrificed each time on 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 12 and 14 days of moulting, and samples (ovary, magnum, uterus and hierarchal follicles) were collected aseptically for the quantitative study by real‐time polymerase chain reaction. The ovary, isthmus, uterus and magnum weight reduced significantly during induced moulting. From the 4 DOM, this reduction was drastic and reached approximately 80% of original weight in the case of ovary, isthmus and magnum and approximately 65% of original weight in the case of uterus on 14 DOM. Ovarian yellow follicles decreased gradually from 1 DOM to 4 DOM, after that no normal yellow follicle was observed in moulted bird. The number of atretic follicles increased gradually during the course of induced moulting, reaching the peak at 5 DOM. The LHR mRNA was detected in non‐gonadal tissues like magnum and uterus. The LHR expression was significantly (p &lt; 0.05) down regulated in ovary, magnum and uterus throughout the treatment. These results indicated that LHR may have a role in reproductive tissue regression during moulting.</description><subject>Animal reproduction</subject><subject>Animals</subject><subject>Chickens - physiology</subject><subject>Female</subject><subject>Females</subject><subject>Gene expression</subject><subject>Gene Expression Regulation - physiology</subject><subject>Hormones</subject><subject>Molting - physiology</subject><subject>Ovarian Follicle - metabolism</subject><subject>Oviducts - metabolism</subject><subject>Poultry</subject><subject>Real-Time Polymerase Chain Reaction</subject><subject>Receptors, LH - genetics</subject><subject>Receptors, LH - metabolism</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>Transcriptome</subject><issn>0936-6768</issn><issn>1439-0531</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkkFv0zAYhiMEYmXwF5AlLlwS7NiO4wOHad1apMLQKJrExXKcL61LGnd2Ah2_gx-M044eOOGLP-t73tef9TpJEMEZievdJiOMyhRzSrIckzzDOWE82z9JJqfG02SCJS3SQhTlWfIihA3GhJdCPE_O8rzEnAs5SX5f7XceQrCuQ5-9a2wLyDVoMfRgO_vLdis0d37rOkC3YGDXO49mEE-2Q3MLXnuz1i26dm1rTQsB6a6O5OrgGcU3P2w9mB4tbQhDbEfvu7XtAS1gtXY-mkAX0HTwI_zRDW0fi5fJs0a3AV497ufJ1-ur5eU8XdzMPlxeLFLDKOdpPT6n0oVklQSmK2mKnGldgcEGSiilFIKwShjWyLKUlBQVxxWBKGa6bgQ9T94efXfe3cfperW1wUDb6g7cEBShRJS04JxH9M0_6MYNvovTHaiCcMxkpMojZbwLwUOjdt5utX9QBKsxObVRY0BqDEiNyalDcmofpa8fLxiqLdQn4d-oIvD-CPyMGT38t7G6nV6MVdSnR70NPexPeu2_q0JQwdXdp5laUvotfpgvakr_AJEMt4c</recordid><startdate>201304</startdate><enddate>201304</enddate><creator>Agarwal, R</creator><creator>Sastry, KVH</creator><creator>Tripathi, V</creator><creator>Singh, R</creator><creator>Saxena, R</creator><creator>Mohan, J</creator><creator>Singh, RP</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>201304</creationdate><title>Expression Profile of Luteinizing Hormone Receptor Gene in Hierarchal Follicles and Regressing Oviduct Tissues of White Leghorn Hens During Moulting</title><author>Agarwal, R ; Sastry, KVH ; Tripathi, V ; Singh, R ; Saxena, R ; Mohan, J ; Singh, RP</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4355-d1587ba694b9e4ab9c624aabec0ce8e8997714b7c4f9889316b50b1e4354adf73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Animal reproduction</topic><topic>Animals</topic><topic>Chickens - physiology</topic><topic>Female</topic><topic>Females</topic><topic>Gene expression</topic><topic>Gene Expression Regulation - physiology</topic><topic>Hormones</topic><topic>Molting - physiology</topic><topic>Ovarian Follicle - metabolism</topic><topic>Oviducts - metabolism</topic><topic>Poultry</topic><topic>Real-Time Polymerase Chain Reaction</topic><topic>Receptors, LH - genetics</topic><topic>Receptors, LH - metabolism</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>Transcriptome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Agarwal, R</creatorcontrib><creatorcontrib>Sastry, KVH</creatorcontrib><creatorcontrib>Tripathi, V</creatorcontrib><creatorcontrib>Singh, R</creatorcontrib><creatorcontrib>Saxena, R</creatorcontrib><creatorcontrib>Mohan, J</creatorcontrib><creatorcontrib>Singh, RP</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Reproduction in domestic animals</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Agarwal, R</au><au>Sastry, KVH</au><au>Tripathi, V</au><au>Singh, R</au><au>Saxena, R</au><au>Mohan, J</au><au>Singh, RP</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression Profile of Luteinizing Hormone Receptor Gene in Hierarchal Follicles and Regressing Oviduct Tissues of White Leghorn Hens During Moulting</atitle><jtitle>Reproduction in domestic animals</jtitle><addtitle>Reprod Domest Anim</addtitle><date>2013-04</date><risdate>2013</risdate><volume>48</volume><issue>2</issue><spage>278</spage><epage>283</epage><pages>278-283</pages><issn>0936-6768</issn><eissn>1439-0531</eissn><abstract>Contents In the present study, the expression profile of luteinizing hormone receptor (LHR) was investigated in the ovary, magnum and uterus and in hierarchcal follicles (F‐1, F‐2, F‐3 and F‐4) of hens subjected to moulting to establish their involvement in moulting and presence in non‐gonadal tissues. Fifty‐two layers (72 weeks) were subjected to moult for a period of 14 days. Four birds were sacrificed each time on 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 12 and 14 days of moulting, and samples (ovary, magnum, uterus and hierarchal follicles) were collected aseptically for the quantitative study by real‐time polymerase chain reaction. The ovary, isthmus, uterus and magnum weight reduced significantly during induced moulting. From the 4 DOM, this reduction was drastic and reached approximately 80% of original weight in the case of ovary, isthmus and magnum and approximately 65% of original weight in the case of uterus on 14 DOM. Ovarian yellow follicles decreased gradually from 1 DOM to 4 DOM, after that no normal yellow follicle was observed in moulted bird. The number of atretic follicles increased gradually during the course of induced moulting, reaching the peak at 5 DOM. The LHR mRNA was detected in non‐gonadal tissues like magnum and uterus. The LHR expression was significantly (p &lt; 0.05) down regulated in ovary, magnum and uterus throughout the treatment. These results indicated that LHR may have a role in reproductive tissue regression during moulting.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>22805579</pmid><doi>10.1111/j.1439-0531.2012.02145.x</doi><tpages>6</tpages></addata></record>
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language eng
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source MEDLINE; Wiley Journals
subjects Animal reproduction
Animals
Chickens - physiology
Female
Females
Gene expression
Gene Expression Regulation - physiology
Hormones
Molting - physiology
Ovarian Follicle - metabolism
Oviducts - metabolism
Poultry
Real-Time Polymerase Chain Reaction
Receptors, LH - genetics
Receptors, LH - metabolism
RNA, Messenger - genetics
RNA, Messenger - metabolism
Transcriptome
title Expression Profile of Luteinizing Hormone Receptor Gene in Hierarchal Follicles and Regressing Oviduct Tissues of White Leghorn Hens During Moulting
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