CXCL13 and CXCR5 are upregulated in PCOS mice ovaries but downregulated following metformin administration

Polycystic ovary syndrome (PCOS) is becoming a common pathology among women, yet its pathogenesis remains enigmatic. The chemokine C-X-C motif ligand 13 (CXCL13) and its receptor type 5 (CXCR5) regulate inflammatory responses but their roles in PCOS remain unknown. Metformin is commonly administered...

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Published in:Molecular and cellular endocrinology Vol. 556; p. 111730
Main Authors: Ullah, Amin, Pervaz, Sadaf, Adu-Gyamfi, Enoch Appiah, Czika, Armin, Guo, Man, Wang, Mei-Jiao, Wang, Ying-Xiong
Format: Journal Article
Language:English
Published: Elsevier B.V 01.10.2022
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ISSN:0303-7207, 1872-8057, 1872-8057
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Abstract Polycystic ovary syndrome (PCOS) is becoming a common pathology among women, yet its pathogenesis remains enigmatic. The chemokine C-X-C motif ligand 13 (CXCL13) and its receptor type 5 (CXCR5) regulate inflammatory responses but their roles in PCOS remain unknown. Metformin is commonly administered to PCOS patients but its mechanism of action remains unclear. Thus, we aimed to determine the expression of CXCL13 and CXCR5 in the ovaries of PCOS mice and to evaluate the therapeutic effect of metformin on them. The study comprised four groups of mice: control, PCOS, PCOS plus metformin, and PCOS plus vehicle. CXCL13 and CXCR5 were found to be elevated in the ovarian tissues of the PCOS mice. Metformin reduced ovarian CXCL13 and CXCR5 expressions in the PCOS mice. Hence, CXCL13 and CXCR5 are potentially involved in PCOS pathogenesis; and metformin may help alleviate the symptoms of PCOS by inhibiting CXCL13 expression and actions. •Serum CXCL13 concentrations were higher in PCOS mice than in normal controls but could be reversed by metformin.•Metformin administration improved hormonal levels and the lipid profile of PCOS mice.•Metformin administration partially resolved ovarian morphology in PCOS mice.
AbstractList Polycystic ovary syndrome (PCOS) is becoming a common pathology among women, yet its pathogenesis remains enigmatic. The chemokine C-X-C motif ligand 13 (CXCL13) and its receptor type 5 (CXCR5) regulate inflammatory responses but their roles in PCOS remain unknown. Metformin is commonly administered to PCOS patients but its mechanism of action remains unclear. Thus, we aimed to determine the expression of CXCL13 and CXCR5 in the ovaries of PCOS mice and to evaluate the therapeutic effect of metformin on them. The study comprised four groups of mice: control, PCOS, PCOS plus metformin, and PCOS plus vehicle. CXCL13 and CXCR5 were found to be elevated in the ovarian tissues of the PCOS mice. Metformin reduced ovarian CXCL13 and CXCR5 expressions in the PCOS mice. Hence, CXCL13 and CXCR5 are potentially involved in PCOS pathogenesis; and metformin may help alleviate the symptoms of PCOS by inhibiting CXCL13 expression and actions.Polycystic ovary syndrome (PCOS) is becoming a common pathology among women, yet its pathogenesis remains enigmatic. The chemokine C-X-C motif ligand 13 (CXCL13) and its receptor type 5 (CXCR5) regulate inflammatory responses but their roles in PCOS remain unknown. Metformin is commonly administered to PCOS patients but its mechanism of action remains unclear. Thus, we aimed to determine the expression of CXCL13 and CXCR5 in the ovaries of PCOS mice and to evaluate the therapeutic effect of metformin on them. The study comprised four groups of mice: control, PCOS, PCOS plus metformin, and PCOS plus vehicle. CXCL13 and CXCR5 were found to be elevated in the ovarian tissues of the PCOS mice. Metformin reduced ovarian CXCL13 and CXCR5 expressions in the PCOS mice. Hence, CXCL13 and CXCR5 are potentially involved in PCOS pathogenesis; and metformin may help alleviate the symptoms of PCOS by inhibiting CXCL13 expression and actions.
Polycystic ovary syndrome (PCOS) is becoming a common pathology among women, yet its pathogenesis remains enigmatic. The chemokine C-X-C motif ligand 13 (CXCL13) and its receptor type 5 (CXCR5) regulate inflammatory responses but their roles in PCOS remain unknown. Metformin is commonly administered to PCOS patients but its mechanism of action remains unclear. Thus, we aimed to determine the expression of CXCL13 and CXCR5 in the ovaries of PCOS mice and to evaluate the therapeutic effect of metformin on them. The study comprised four groups of mice: control, PCOS, PCOS plus metformin, and PCOS plus vehicle. CXCL13 and CXCR5 were found to be elevated in the ovarian tissues of the PCOS mice. Metformin reduced ovarian CXCL13 and CXCR5 expressions in the PCOS mice. Hence, CXCL13 and CXCR5 are potentially involved in PCOS pathogenesis; and metformin may help alleviate the symptoms of PCOS by inhibiting CXCL13 expression and actions. •Serum CXCL13 concentrations were higher in PCOS mice than in normal controls but could be reversed by metformin.•Metformin administration improved hormonal levels and the lipid profile of PCOS mice.•Metformin administration partially resolved ovarian morphology in PCOS mice.
Polycystic ovary syndrome (PCOS) is becoming a common pathology among women, yet its pathogenesis remains enigmatic. The chemokine C-X-C motif ligand 13 (CXCL13) and its receptor type 5 (CXCR5) regulate inflammatory responses but their roles in PCOS remain unknown. Metformin is commonly administered to PCOS patients but its mechanism of action remains unclear. Thus, we aimed to determine the expression of CXCL13 and CXCR5 in the ovaries of PCOS mice and to evaluate the therapeutic effect of metformin on them. The study comprised four groups of mice: control, PCOS, PCOS plus metformin, and PCOS plus vehicle. CXCL13 and CXCR5 were found to be elevated in the ovarian tissues of the PCOS mice. Metformin reduced ovarian CXCL13 and CXCR5 expressions in the PCOS mice. Hence, CXCL13 and CXCR5 are potentially involved in PCOS pathogenesis; and metformin may help alleviate the symptoms of PCOS by inhibiting CXCL13 expression and actions.
ArticleNumber 111730
Author Wang, Ying-Xiong
Wang, Mei-Jiao
Pervaz, Sadaf
Guo, Man
Czika, Armin
Ullah, Amin
Adu-Gyamfi, Enoch Appiah
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  fullname: Ullah, Amin
  organization: Department of Reproductive Sciences, School of Public Health, Chongqing Medical University, Chongqing, People’s Republic of China
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  givenname: Sadaf
  surname: Pervaz
  fullname: Pervaz, Sadaf
  organization: Department of Reproductive Sciences, School of Public Health, Chongqing Medical University, Chongqing, People’s Republic of China
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  givenname: Enoch Appiah
  surname: Adu-Gyamfi
  fullname: Adu-Gyamfi, Enoch Appiah
  organization: Department of Reproductive Sciences, School of Public Health, Chongqing Medical University, Chongqing, People’s Republic of China
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  givenname: Armin
  surname: Czika
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  givenname: Mei-Jiao
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  fullname: Wang, Mei-Jiao
  email: meijiaowang@cqmu.edu.cn
  organization: Joint International Research Laboratory of Reproduction and Development, School of Public Health, Chongqing Medical University, Chongqing, People’s Republic of China
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  givenname: Ying-Xiong
  surname: Wang
  fullname: Wang, Ying-Xiong
  email: yxwang@cqmu.edu.cn
  organization: Department of Reproductive Sciences, School of Public Health, Chongqing Medical University, Chongqing, People’s Republic of China
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Keywords CXCR5
Polycystic ovarian syndrome
Inflammation
Metformin
Extracellular-signaling-related kinase
CXCL13
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Snippet Polycystic ovary syndrome (PCOS) is becoming a common pathology among women, yet its pathogenesis remains enigmatic. The chemokine C-X-C motif ligand 13...
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SubjectTerms CXCL13
CXCR5
endocrinology
Extracellular-signaling-related kinase
Inflammation
mechanism of action
Metformin
pathogenesis
Polycystic ovarian syndrome
polycystic ovary syndrome
therapeutics
Title CXCL13 and CXCR5 are upregulated in PCOS mice ovaries but downregulated following metformin administration
URI https://dx.doi.org/10.1016/j.mce.2022.111730
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