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. 2024 Jan 2;55(1):51–67. doi: 10.1007/s10735-023-10171-4

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© The Author(s) 2023

Open Access This 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/.

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Fig. 11 — Working model. VNS improves VSMC metabolism and arteriogenesis in the infarcted heart through m/n-AChR-Akt1-SDF-1α. VNS and acetylcholine (ACh)-induced SDF-1α expression optimized the VSMC metabolism pattern characterized by increased CPT1α/β and Glut1/4 expression while promoting arteriogenesis in the infarcted heart, which was related to the ACh/m/nAChR/Akt signaling cascade