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. 2023 Sep 27;11:212. doi: 10.1186/s40168-023-01659-y

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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/. The Creative Commons Public Domain Dedication waiver (http://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.

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Fig. 7 — Diagram for the amelioration of gut metabolite 3-Hydroxyphenylacetic acid on the aging-related spermatogenic dysfunction. The altered GM abundance in intestine were closely related to the changed gut bacteria-derived metabolite, 3-Hydroxyphenylacetic acid (3-HPAA). 3-HPAA promotes GPX4-mediated reduction of intracellular phospholipid hydroperoxides (PL-OOH) and 3-HPAA-related metabolic pathway may alleviate the impaired spermatogenesis of aging mice through regulation of ferroptosis