ORIGINAL RESEARCH article
Front. Vet. Sci.
Sec. Animal Nutrition and Metabolism
This article is part of the Research TopicThreats and Strategies of Nutritional Metabolic Disorders and Poisoning Diseases in RuminantsView all 20 articles
High-grain diet–induced ruminal acidosis triggers systemic inflammation and serum metabolic reprogramming in dairy cows
Provisionally accepted- 1Shanxi Agricultural University College of Animal Science, Jinzhong, China
- 2Gansu Agricultural University, Lanzhou, China
- 3Inner Mongolia Agricultural University, Hohhot, China
Select one of your emails
You have multiple emails registered with Frontiers:
Notify me on publication
Please enter your email address:
If you already have an account, please login
You don't have a Frontiers account ? You can register here
High-grain diets are widely used to meet the energy demands of high-producing dairy cows; however, excessive grain intake predisposes cows to ruminal acidosis and subsequent systemic inflammation, compromising health and productivity. This study aimed to characterize systemic inflammatory responses and associated serum metabolic alterations induced by high-grain feeding. Fourteen mid-lactation dairy cows fitted with permanent rumen fistulas were subjected to a gradual increase in dietary corn grain to induce ruminal acidosis. Blood samples were collected under normal and acidosis conditions, inflammatory biomarkers were quantified using ELISA, and serum metabolomic profiles were analyzed by GC-TOF/MS. Rumen pH decreased significantly with increasing dietary corn grain (P < 0.05), confirming the successful induction of ruminal acidosis. Serum lipopolysaccharide (LPS) concentrations exhibited an inverted bell-shaped pattern during the induction process (P < 0.05), while concentrations of acute phase proteins, including serum amyloid A (SAA), C-reactive protein (CRP), and haptoglobin (Hp), increased markedly (P < 0.05), indicating the development of systemic inflammation. Metabolomic analysis revealed a clear separation between normal and acidosis states, with 37 significantly different metabolites identified. Correlation analysis showed that multiple serum metabolites were closely associated with ruminal pH and inflammatory indicators, particularly SAA, CRP, and Hp. Lipid-and amino acid–related metabolites were positively correlated with inflammatory parameters, whereas several organic acids showed negative correlations, suggesting coordinated metabolic reprogramming during high-grain–induced inflammation. Biomarker analysis identified D-glycerol-1-phosphate and 4-hydroxypyridine as potential serum biomarkers capable of discriminating acidosis-associated metabolic alterations. In conclusion, a gradual increase in dietary corn grain induces progressive systemic inflammation and pronounced disturbances in serum metabolic homeostasis in lactating dairy cows. These findings highlight the tight linkage between rumen dysfunction and host metabolic regulation and provide potential blood-based biomarkers for early detection of inflammation associated with high-grain feeding.
Keywords: High-grain diet, Holstein dairy cow, rumen acidosis, serum metabolomics, systemic inflammation
Received: 25 Dec 2025; Accepted: 30 Jan 2026.
Copyright: © 2026 Zhang, Xie and LI. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence: Xueqiang LI
Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
