Skip to main content
Log in

TRPC5 mediates endothelium-dependent contraction in the carotid artery of diet-induced obese mice

  • Article
  • Published:
Hypertension Research Submit manuscript

Abstract

Little is known about the contribution of the transient receptor potential canonical channel isoform 5 (TRPC5), a Ca2+-sensitive channel, to vasoconstriction in obesity. In this study, we found that the TRPC5 expression and carotid artery contraction of diet-induced obese (DIO) mice were significantly higher than those of wild-type mice. Endothelium-dependent vasocontraction was inhibited by the TRPC5 inhibitor clemizole and the knockout of TRPC5 in DIO mouse carotid arteries, while activation of TRPC5 enhanced contraction in wild-type mice. TRPC5-regulated vasocontraction can be inhibited by the ROS scavenger NAC and the COX-2 inhibitor NS-398. Our study suggested that upregulation of TRPC5 contributes to endothelium-dependent contraction, which is involved in ROS production and COX-2 expression in DIO mouse carotid arteries. From these results, we speculated that TRPC5 mediated endothelium-dependent contraction in the carotid artery of DIO mice, which was achieved by increasing the levels of ROS and COX-2 expression.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6

Similar content being viewed by others

References

  1. Barton M, Baretella O, Meyer MR. Obesity and risk of vascular disease: importance of endothelium-dependent vasoconstriction. Br J Pharm. 2012;165:591–602.

    Article  CAS  Google Scholar 

  2. Vanhoutte PM, Shimokawa H, Tang EHC, Feletou M. Endothelial dysfunction and vascular disease. Acta Physiologica. 2009;196:193–222.

    Article  CAS  PubMed  Google Scholar 

  3. Traupe T, Lang M, Goettsch W, Münter K, Morawietz H, Vetter W, et al. Obesity increases prostanoid-mediated vasoconstriction and vascular thromboxane receptor gene expression. J hypertension. 2002;20:2239–45.

    Article  CAS  Google Scholar 

  4. Thébault S. Minireview: insights into the role of TRP channels in the retinal circulation and function. Neurosc Lett. 2021;765:136285.

  5. Liang C, Zhang Y, Zhuo D, Lo CY, Yu L, Lau CW, et al. Endothelial cell transient receptor potential channel C5 (TRPC5) is essential for endothelium-dependent contraction in mouse carotid arteries. Biochem Pharm. 2019;159:11–24.

    Article  CAS  PubMed  Google Scholar 

  6. Li Z, Guo G, Wang H, Si X, Zhou G, Xiong Y, et al. TRPC5 channel modulates endothelial cells senescence. Eur J Pharmacol. 2017;802:27–35.

    Article  CAS  PubMed  Google Scholar 

  7. Lau OC, Shen B, Wong CO, Tjong YW, Lo CY, Wang HC, et al. TRPC5 channels participate in pressure-sensing in aortic baroreceptors. Nat Commun. 2016;7:11947.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  8. Riccio A, Li Y, Moon J, Kim KS, Smith KS, Rudolph U, et al. Essential role for TRPC5 in amygdala function and fear-related behavior. Cell. 2009;137:761–72.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  9. Zhang P, Sun C, Li H, Tang C, Kan H, Yang Z, et al. TRPV4 (transient receptor potential vanilloid 4) mediates endothelium-dependent contractions in the aortas of hypertensive mice. Hypertension. 2018;71:134–42.

    Article  CAS  PubMed  Google Scholar 

  10. Minard A, Bauer CC, Chuntharpursat-Bon E, Pickles IB, Wright DJ, Ludlow MJ, et al. Potent, selective, and subunit-dependent activation of TRPC5 channels by a xanthine derivative. Br J Pharm. 2019;176:3924–38.

    Article  CAS  Google Scholar 

  11. Sun GY, Chuang DY, Zong Y, Jiang J, Lee JC, Gu Z, et al. Role of cytosolic phospholipase A2 in oxidative and inflammatory signaling pathways in different cell types in the central nervous system. Mol Neurobiol. 2014;50:6–14.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  12. Liu Y, Xu Y, Thilo F, Friis UG, Jensen BL, Scholze A, et al. Erythropoietin increases expression and function of transient receptor potential canonical 5 channels. Hypertension. 2011;58:317–24.

    Article  CAS  PubMed  Google Scholar 

  13. Wong MS, Vanhoutte PM. COX-mediated endothelium-dependent contractions: from the past to recent discoveries. Acta Pharm Sin. 2010;31:1095–102.

    Article  Google Scholar 

  14. Tang EH, Vanhoutte PM. Prostanoids and reactive oxygen species: team players in endothelium-dependent contractions. Pharm Ther. 2009;122:140–9.

    Article  CAS  Google Scholar 

  15. Chen M, Xiang L, Wu G, Liao Y, Cai Y. Puerarin inhibits endothelium-dependent contractions in mouse carotid arteries. Med Sci Monit. 2020;26:e923163.

    CAS  PubMed  PubMed Central  Google Scholar 

  16. Zhou Y, Castonguay P, Sidhom E, Clark A, Dvela-Levitt M, Kim S, et al. A small-molecule inhibitor of TRPC5 ion channels suppresses progressive kidney disease in animal models. Science. 2017;358:1332–6.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  17. Qi J, Cui J, Mi B, Yan X, Xu W, Ma H, et al. Isoliquiritigenin inhibits atherosclerosis by blocking TRPC5 channel expression. Cardiovasc Ther. 2020;2020:1926249.

    Article  PubMed  PubMed Central  Google Scholar 

  18. Liu FF, Ma ZY, Li DL, Feng JB, Zhang K, Wang R, et al. Differential expression of TRPC channels in the left ventricle of spontaneously hypertensive rats. Mol Biol Rep. 2010;37:2645–51.

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgements

We thank Professor David E. Clapham (Harvard Medical School, USA) for giving us the TRPC5-knockout (TRPC5-/-) mice as a gift. We appreciate Dr Chunlei Tang (Jiangnan University, China) for assistance with the preparation of the AM237 compound.

Funding

This work was supported by the National Natural Science Foundation of China (81622007, 81960662, 82000291, and 82025005), the Chang Jiang Scholars Program (Q2015106), the Fundamental Research Funds for the Central Universities (JUSRP51704A), the National First-Class Discipline Program of Food Science and Technology (JUFSTR20180101), the Fundamental Research Funds for Young Scholars of Jiangnan University (JUSRP12046), and the Natural Science Foundation for Young Scholars of Jiangsu Province (BK20190596).

Author information

Authors and Affiliations

Authors

Contributions

The experimental design and operation of this study were mainly completed by YC and SW. The paper was written by YC and SW. YZ and XM guided the overall idea of the study. FY and KZ put forward valuable opinions on the writing of the article. XM provided a critical reading of the manuscript.

Corresponding author

Correspondence to Xin Ma.

Ethics declarations

Conflict of interest

The authors declare no competing interests.

Additional information

Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary information

Rights and permissions

Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Chu, Y., Wang, S., Zhu, Y. et al. TRPC5 mediates endothelium-dependent contraction in the carotid artery of diet-induced obese mice. Hypertens Res 45, 1945–1953 (2022). https://doi.org/10.1038/s41440-022-01017-9

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/s41440-022-01017-9

  • Springer Nature Singapore Pte Ltd.

Keywords

This article is cited by

Navigation