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Upregulation of carbonic anhydrase 1 beneficial for depressive disorder

Carbonic Anhydrase 1 (CAR1) is a zinc-metalloenzyme that catalyzes the hydration of carbon dioxide, and the alteration of CAR1 has been implicated in neuropsychiatric disorders. However, the mechanism underlying the role of CAR1 in major depressive disorder (MDD) remains largely unknown. In this stu...

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Autores principales: Cheng, Ke, Wang, Yue, He, Yong, Tian, Yu, Li, Junjie, Chen, Chong, Xu, Xingzhe, Wu, Zhonghao, Yu, Heming, Chen, Xiangyu, Wu, Yili, Song, Weihong, Dong, Zhifang, Xu, Huatai, Xie, Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10071615/
https://www.ncbi.nlm.nih.gov/pubmed/37013604
http://dx.doi.org/10.1186/s40478-023-01545-6
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author Cheng, Ke
Wang, Yue
He, Yong
Tian, Yu
Li, Junjie
Chen, Chong
Xu, Xingzhe
Wu, Zhonghao
Yu, Heming
Chen, Xiangyu
Wu, Yili
Song, Weihong
Dong, Zhifang
Xu, Huatai
Xie, Peng
author_facet Cheng, Ke
Wang, Yue
He, Yong
Tian, Yu
Li, Junjie
Chen, Chong
Xu, Xingzhe
Wu, Zhonghao
Yu, Heming
Chen, Xiangyu
Wu, Yili
Song, Weihong
Dong, Zhifang
Xu, Huatai
Xie, Peng
author_sort Cheng, Ke
collection PubMed
description Carbonic Anhydrase 1 (CAR1) is a zinc-metalloenzyme that catalyzes the hydration of carbon dioxide, and the alteration of CAR1 has been implicated in neuropsychiatric disorders. However, the mechanism underlying the role of CAR1 in major depressive disorder (MDD) remains largely unknown. In this study, we report the decreased level of CAR1 in MDD patients and depression-like model rodents. We found that CAR1 is expressed in hippocampal astrocytes and CAR1 regulates extracellular bicarbonate concentration and pH value in the partial hilus. Ablation of the CAR1 gene increased the activity of granule cells via decreasing their miniature inhibitory postsynaptic currents (mIPSC), and caused depression-like behaviors in CAR1-knockout mice. Astrocytic CAR1 expression rescued the deficits in mIPSCs of granule cells and reduced depression-like behaviors in CAR1 deficient mice. Furthermore, pharmacological activation of CAR1 and overexpression of CAR1 in the ventral hippocampus of mice improved depressive behaviors. These findings uncover a critical role of CAR1 in the MDD pathogenesis and its therapeutic potential. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40478-023-01545-6.
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spelling pubmed-100716152023-04-05 Upregulation of carbonic anhydrase 1 beneficial for depressive disorder Cheng, Ke Wang, Yue He, Yong Tian, Yu Li, Junjie Chen, Chong Xu, Xingzhe Wu, Zhonghao Yu, Heming Chen, Xiangyu Wu, Yili Song, Weihong Dong, Zhifang Xu, Huatai Xie, Peng Acta Neuropathol Commun Research Carbonic Anhydrase 1 (CAR1) is a zinc-metalloenzyme that catalyzes the hydration of carbon dioxide, and the alteration of CAR1 has been implicated in neuropsychiatric disorders. However, the mechanism underlying the role of CAR1 in major depressive disorder (MDD) remains largely unknown. In this study, we report the decreased level of CAR1 in MDD patients and depression-like model rodents. We found that CAR1 is expressed in hippocampal astrocytes and CAR1 regulates extracellular bicarbonate concentration and pH value in the partial hilus. Ablation of the CAR1 gene increased the activity of granule cells via decreasing their miniature inhibitory postsynaptic currents (mIPSC), and caused depression-like behaviors in CAR1-knockout mice. Astrocytic CAR1 expression rescued the deficits in mIPSCs of granule cells and reduced depression-like behaviors in CAR1 deficient mice. Furthermore, pharmacological activation of CAR1 and overexpression of CAR1 in the ventral hippocampus of mice improved depressive behaviors. These findings uncover a critical role of CAR1 in the MDD pathogenesis and its therapeutic potential. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40478-023-01545-6. BioMed Central 2023-04-03 /pmc/articles/PMC10071615/ /pubmed/37013604 http://dx.doi.org/10.1186/s40478-023-01545-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Cheng, Ke
Wang, Yue
He, Yong
Tian, Yu
Li, Junjie
Chen, Chong
Xu, Xingzhe
Wu, Zhonghao
Yu, Heming
Chen, Xiangyu
Wu, Yili
Song, Weihong
Dong, Zhifang
Xu, Huatai
Xie, Peng
Upregulation of carbonic anhydrase 1 beneficial for depressive disorder
title Upregulation of carbonic anhydrase 1 beneficial for depressive disorder
title_full Upregulation of carbonic anhydrase 1 beneficial for depressive disorder
title_fullStr Upregulation of carbonic anhydrase 1 beneficial for depressive disorder
title_full_unstemmed Upregulation of carbonic anhydrase 1 beneficial for depressive disorder
title_short Upregulation of carbonic anhydrase 1 beneficial for depressive disorder
title_sort upregulation of carbonic anhydrase 1 beneficial for depressive disorder
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10071615/
https://www.ncbi.nlm.nih.gov/pubmed/37013604
http://dx.doi.org/10.1186/s40478-023-01545-6
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