Food deprivation differentially modulates gene expression of LPXRFa and kisspeptin systems in the brain-pituitary axis of half-smooth tongue sole (Cynoglossus semilaevis)

LPXRFa, also known as gonadotropin-inhibitory hormone (GnIH), and kisspeptin (Kiss) are two major hypothalamic peptides that modulate the reproductive axis of vertebrates, including teleosts. However, little information is available regarding the actions of nutritional status on the regulation of th...

Full description

Bibliographic Details
Main Authors: Bin Wang, Aijun Cui, Yongjiang Xu, Yaxing Zhang, Yan Jiang, Xuezhou Liu
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-03-01
Series:Frontiers in Endocrinology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fendo.2023.1099832/full
_version_ 1797861010017615872
author Bin Wang
Bin Wang
Aijun Cui
Aijun Cui
Yongjiang Xu
Yongjiang Xu
Yaxing Zhang
Yan Jiang
Yan Jiang
Xuezhou Liu
Xuezhou Liu
author_facet Bin Wang
Bin Wang
Aijun Cui
Aijun Cui
Yongjiang Xu
Yongjiang Xu
Yaxing Zhang
Yan Jiang
Yan Jiang
Xuezhou Liu
Xuezhou Liu
author_sort Bin Wang
collection DOAJ
description LPXRFa, also known as gonadotropin-inhibitory hormone (GnIH), and kisspeptin (Kiss) are two major hypothalamic peptides that modulate the reproductive axis of vertebrates, including teleosts. However, little information is available regarding the actions of nutritional status on the regulation of these two neuroendocrine systems in fish. Herein, we assessed the effects of starvation and refeeding on the expression of lpxrfa, kiss2 and their receptors (lpxrfa-r and kiss2r respectively) at the brain-pituitary level of half-smooth tongue sole (Cynoglossus semilaevis). Food deprivation for 4 weeks induced a rise in brain lpxrfa as well as brain and pituitary lpxrfa-r mRNA levels, and refeeding restored brain lpxrfa and lpxrfa-r expression back to normal. However, pituitary lpxrfa-r mRNA levels still remained high after 1 week of refeeding. Neither lpxrfa nor kiss2 transcripts in the pituitary were altered by fasting, but their mRNA levels increased significantly after 1 week of refeeding, and declined back to the control levels after 2 weeks of refeeding. None of brain kiss2 and kiss2r along with pituitary kiss2r transcripts were modified by the nutritional status. In summary, our results revealed an interaction between energy status and the elements of LPXRFa and Kiss systems in the brain-pituitary axis of half-smooth tongue sole. Food deprivation and refeeding differentially regulated the two systems, which provided additional evidence for the involvement of the LPXRFa and Kiss systems in the regulation of reproduction by energy balance in non-mammalian species.
first_indexed 2024-04-09T21:55:09Z
format Article
id doaj.art-4bd15e81b61245e9982323e05b4f2581
institution Directory Open Access Journal
issn 1664-2392
language English
last_indexed 2024-04-09T21:55:09Z
publishDate 2023-03-01
publisher Frontiers Media S.A.
record_format Article
series Frontiers in Endocrinology
spelling doaj.art-4bd15e81b61245e9982323e05b4f25812023-03-24T05:59:11ZengFrontiers Media S.A.Frontiers in Endocrinology1664-23922023-03-011410.3389/fendo.2023.10998321099832Food deprivation differentially modulates gene expression of LPXRFa and kisspeptin systems in the brain-pituitary axis of half-smooth tongue sole (Cynoglossus semilaevis)Bin Wang0Bin Wang1Aijun Cui2Aijun Cui3Yongjiang Xu4Yongjiang Xu5Yaxing Zhang6Yan Jiang7Yan Jiang8Xuezhou Liu9Xuezhou Liu10Key Laboratory of Sustainable Development of Marine Fisheries, Ministry of Agriculture and Rural Affairs, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao, ChinaJoint Laboratory for Deep Blue Fishery Engineering, Pilot National Laboratory for Marine Science and Technology (Qingdao), Qingdao, ChinaKey Laboratory of Sustainable Development of Marine Fisheries, Ministry of Agriculture and Rural Affairs, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao, ChinaJoint Laboratory for Deep Blue Fishery Engineering, Pilot National Laboratory for Marine Science and Technology (Qingdao), Qingdao, ChinaKey Laboratory of Sustainable Development of Marine Fisheries, Ministry of Agriculture and Rural Affairs, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao, ChinaJoint Laboratory for Deep Blue Fishery Engineering, Pilot National Laboratory for Marine Science and Technology (Qingdao), Qingdao, ChinaKey Laboratory of Sustainable Development of Marine Fisheries, Ministry of Agriculture and Rural Affairs, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao, ChinaKey Laboratory of Sustainable Development of Marine Fisheries, Ministry of Agriculture and Rural Affairs, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao, ChinaJoint Laboratory for Deep Blue Fishery Engineering, Pilot National Laboratory for Marine Science and Technology (Qingdao), Qingdao, ChinaKey Laboratory of Sustainable Development of Marine Fisheries, Ministry of Agriculture and Rural Affairs, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao, ChinaJoint Laboratory for Deep Blue Fishery Engineering, Pilot National Laboratory for Marine Science and Technology (Qingdao), Qingdao, ChinaLPXRFa, also known as gonadotropin-inhibitory hormone (GnIH), and kisspeptin (Kiss) are two major hypothalamic peptides that modulate the reproductive axis of vertebrates, including teleosts. However, little information is available regarding the actions of nutritional status on the regulation of these two neuroendocrine systems in fish. Herein, we assessed the effects of starvation and refeeding on the expression of lpxrfa, kiss2 and their receptors (lpxrfa-r and kiss2r respectively) at the brain-pituitary level of half-smooth tongue sole (Cynoglossus semilaevis). Food deprivation for 4 weeks induced a rise in brain lpxrfa as well as brain and pituitary lpxrfa-r mRNA levels, and refeeding restored brain lpxrfa and lpxrfa-r expression back to normal. However, pituitary lpxrfa-r mRNA levels still remained high after 1 week of refeeding. Neither lpxrfa nor kiss2 transcripts in the pituitary were altered by fasting, but their mRNA levels increased significantly after 1 week of refeeding, and declined back to the control levels after 2 weeks of refeeding. None of brain kiss2 and kiss2r along with pituitary kiss2r transcripts were modified by the nutritional status. In summary, our results revealed an interaction between energy status and the elements of LPXRFa and Kiss systems in the brain-pituitary axis of half-smooth tongue sole. Food deprivation and refeeding differentially regulated the two systems, which provided additional evidence for the involvement of the LPXRFa and Kiss systems in the regulation of reproduction by energy balance in non-mammalian species.https://www.frontiersin.org/articles/10.3389/fendo.2023.1099832/fullLPXRFaLPXRFa receptorkisspeptinkisspeptin receptorCynoglossus semilaevis
spellingShingle Bin Wang
Bin Wang
Aijun Cui
Aijun Cui
Yongjiang Xu
Yongjiang Xu
Yaxing Zhang
Yan Jiang
Yan Jiang
Xuezhou Liu
Xuezhou Liu
Food deprivation differentially modulates gene expression of LPXRFa and kisspeptin systems in the brain-pituitary axis of half-smooth tongue sole (Cynoglossus semilaevis)
Frontiers in Endocrinology
LPXRFa
LPXRFa receptor
kisspeptin
kisspeptin receptor
Cynoglossus semilaevis
title Food deprivation differentially modulates gene expression of LPXRFa and kisspeptin systems in the brain-pituitary axis of half-smooth tongue sole (Cynoglossus semilaevis)
title_full Food deprivation differentially modulates gene expression of LPXRFa and kisspeptin systems in the brain-pituitary axis of half-smooth tongue sole (Cynoglossus semilaevis)
title_fullStr Food deprivation differentially modulates gene expression of LPXRFa and kisspeptin systems in the brain-pituitary axis of half-smooth tongue sole (Cynoglossus semilaevis)
title_full_unstemmed Food deprivation differentially modulates gene expression of LPXRFa and kisspeptin systems in the brain-pituitary axis of half-smooth tongue sole (Cynoglossus semilaevis)
title_short Food deprivation differentially modulates gene expression of LPXRFa and kisspeptin systems in the brain-pituitary axis of half-smooth tongue sole (Cynoglossus semilaevis)
title_sort food deprivation differentially modulates gene expression of lpxrfa and kisspeptin systems in the brain pituitary axis of half smooth tongue sole cynoglossus semilaevis
topic LPXRFa
LPXRFa receptor
kisspeptin
kisspeptin receptor
Cynoglossus semilaevis
url https://www.frontiersin.org/articles/10.3389/fendo.2023.1099832/full
work_keys_str_mv AT binwang fooddeprivationdifferentiallymodulatesgeneexpressionoflpxrfaandkisspeptinsystemsinthebrainpituitaryaxisofhalfsmoothtonguesolecynoglossussemilaevis
AT binwang fooddeprivationdifferentiallymodulatesgeneexpressionoflpxrfaandkisspeptinsystemsinthebrainpituitaryaxisofhalfsmoothtonguesolecynoglossussemilaevis
AT aijuncui fooddeprivationdifferentiallymodulatesgeneexpressionoflpxrfaandkisspeptinsystemsinthebrainpituitaryaxisofhalfsmoothtonguesolecynoglossussemilaevis
AT aijuncui fooddeprivationdifferentiallymodulatesgeneexpressionoflpxrfaandkisspeptinsystemsinthebrainpituitaryaxisofhalfsmoothtonguesolecynoglossussemilaevis
AT yongjiangxu fooddeprivationdifferentiallymodulatesgeneexpressionoflpxrfaandkisspeptinsystemsinthebrainpituitaryaxisofhalfsmoothtonguesolecynoglossussemilaevis
AT yongjiangxu fooddeprivationdifferentiallymodulatesgeneexpressionoflpxrfaandkisspeptinsystemsinthebrainpituitaryaxisofhalfsmoothtonguesolecynoglossussemilaevis
AT yaxingzhang fooddeprivationdifferentiallymodulatesgeneexpressionoflpxrfaandkisspeptinsystemsinthebrainpituitaryaxisofhalfsmoothtonguesolecynoglossussemilaevis
AT yanjiang fooddeprivationdifferentiallymodulatesgeneexpressionoflpxrfaandkisspeptinsystemsinthebrainpituitaryaxisofhalfsmoothtonguesolecynoglossussemilaevis
AT yanjiang fooddeprivationdifferentiallymodulatesgeneexpressionoflpxrfaandkisspeptinsystemsinthebrainpituitaryaxisofhalfsmoothtonguesolecynoglossussemilaevis
AT xuezhouliu fooddeprivationdifferentiallymodulatesgeneexpressionoflpxrfaandkisspeptinsystemsinthebrainpituitaryaxisofhalfsmoothtonguesolecynoglossussemilaevis
AT xuezhouliu fooddeprivationdifferentiallymodulatesgeneexpressionoflpxrfaandkisspeptinsystemsinthebrainpituitaryaxisofhalfsmoothtonguesolecynoglossussemilaevis