Thermal stress alters ruminal function and physiology, compromising health and productivity. Methionine enhances endogenous antioxidant synthesis, whereas guanidinoacetic acid (GAA) supports cellular ATP production. Because methionine serves as a methyl donor for the conversion of GAA to creatine, both nutrients are linked to cellular metabolism and antioxidant defense. The objective was to determine effects of rumen-protected methionine (RPM; Mepron®, Evonik) and GAA (GuanAMINO®, ≥ 97% GAA, ∼1% starch, ∼1% moisture; Evonik), fed alone or in combination during heat stress (HS) on production, thermoregulation, ruminal biopolymer-degrading enzymes and microbiota, ruminal papillae gene expression and cystathionine β-synthase (CBS) activity, and plasma biomarkers. Milk, blood, ruminal fluid and papillae were collected to evaluate lactational, metabolic, microbial, and molecular responses. Ten multiparous Holstein cows (5 intact and 5 with a ruminal cannula; 122 ± 28 DIM, 41.8 ± 3.7 kg milk/d) were used in a replicated 5 × 5 Latin square with 23-d periods (16 d thermoneutral, 7 d HS) and 5 treatments: thermoneutral control (CON-TN), HS control (CON-HS), RPM-HS (RPM at 0.10% of DM), GAA-HS (25 g GAA/d), MIX-HS (RPM at 0.10% of DM plus 25 g GAA/d). Electric heat blankets (EHB) operating at the highest setting (∼40°C) were used to induce HS. Data were analyzed using PROC MIXED (SAS v9.4) with preplanned contrasts: CON-HS vs. CON-TN, RPM-HS vs. CON-HS, RPM-HS vs. GAA-HS, and MIX-HS vs. CON-HS. Compared with CON-TN, CON-HS cows had greater rectal (+0.32°C) and vaginal (+0.34°C) temperatures and respiration rate (+11 beats/min). These variables did not differ among HS treatments. Compared with CON-TN, CON-HS cows had lower milk yield (-3.9 kg/d), milk protein concentration (-0.22 percentage units), and milk protein yield (-0.11 kg/d), whereas MUN was greater (+2.4 mg/dL). Compared with CON-HS, RPM-HS increased milk protein (+0.28 percentage units), casein (+0.11 percentage units), and protein yield (+0.12 kg/d). Milk protein concentration also was greater in RPM-HS than GAA-HS. Total plasma AA concentrations did not differ among treatments (2,056 ± 89 µM), but citrulline concentration was greater in CON-HS than CON-TN (69 vs. 55 µM). Feeding RPM-HS increased plasma cystine concentration compared with CON-HS (24.4 vs. 18.8 µM). At the ruminal level, compared with CON-TN, CON-HS increased the molar proportions of iso-butyrate and isovalerate, and the abundance of Rumicoccus flavefaciens and Succinimonas amylolytica. These variables were not affected by feeding RPM, GAA, or MIX; however, relative to CON-HS, RPM-HS increased cellulase activity and tended to increase xylanase activity. The abundance of Megaspheara elsdenii was greater and Succinimonas amylolytica lower in RPM-HS than CON-HS, whereas GAA-HS increased abundance of Streptococcus bovis approximately 3-fold relative to CON-HS. Ruminal papillae CBS activity more than doubled in CON-HS compared with CON-TN. The HS did not affect mRNA abundance of the 28 target genes evaluated. In contrast, RPM-HS and, to a greater extent, MIX-HS induced coordinated molecular remodeling characterized by upregulation of genes involved in polyamine synthesis, antioxidant responses, and tight-junction signaling. Overall, RPM improved milk protein synthesis and metabolic resilience during HS, whereas MIX primarily enhanced epithelial adaptative responses without additional lactational benefits.
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