PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
September 16, 2025Animals2 citationsOpen Access

Tissue-Specific Mitochondrial Functionality and Mitochondrial-Related Gene Profiles in Response to Maternal Nutrition and One-Carbon Metabolite Supplementation During Early Pregnancy in Heifers

View Full Paper
KSKazi Sarjana SafainMCMatthew S CrouseMHMara R Hirchert

Key Points

  • OCM supplementation leads to improved mitochondrial respiration in fetal liver, enhancing energy metabolism.
  • Fetal muscle exhibited downregulated mitochondria-related genes, reflecting transcriptional reprogramming without functional changes.
  • Maternal nutritional status affected mitochondrial function, with variations noted between control and restricted gain groups.
  • This research highlights early gestation’s importance for nutritional interventions to optimize metabolic outcomes in livestock.

Abstract

Background: Mitochondria are essential for fetal development, regulating energy metabolism and metabolic programming. This study examined how maternal nutrition and one-carbon metabolite (OCM) supplementation during early gestation affect mitochondrial function in fetal liver and muscle at day 161 of gestation in beef heifers. Methods: Twenty-nine crossbred Angus heifers were assigned to one of four treatments in a 2 × 2 factorial design: control (CON; 0.45 kg/day ADG) or restricted gain (RES; −0.23 kg/day), with or without OCM supplementation. Treatments were applied from breeding to day 63 of gestation, after which all heifers received a common diet. Fetal liver and muscle tissues were collected at day 161. Mitochondrial respiration (Seahorse assay), mtDNA copy number (qPCR), and mitochondria-related gene expression (RNA-seq) were assessed. Results: In fetal liver, state 3 respiration was highest in CON + OCM, while state 4o respiration was lowest in RES + OCM (p ≤ 0.05). mtDNA copy number was greater in RES and +OCM groups. In fetal muscle, mtDNA copy number was influenced by gain, but respiration was unaffected. Transcriptomic analysis revealed more mitochondria-related differentially expressed genes (mtDEGs) in fetal muscle than liver (90% versus 10% of total mtDEG), with most genes downregulated in the RES and +OCM groups compared to the CON and −OCM groups (FDR ≤ 0.10). Conclusions: OCM supplementation enhanced mitochondrial respiration and biogenesis in fetal liver, likely via post-translational mechanisms. In contrast, fetal muscle showed downregulation of mitochondria-related genes without functional changes, indicating transcriptional reprogramming with potential effects on later metabolic function. These results underscore early gestation as a critical window for OCM-based nutritional interventions to improve metabolic outcomes in livestock.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Safain et al. (2025) studied this question.

synapsesocial.com/papers/68d4508231b076d99fa5815fhttps://doi.org/10.3390/ani15182689
Ask AI
Helpful
Bookmark
Share
View Full Paper

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1The supply of choline is important for fetal progenitor cells2011 · 78 citations
  2. 2Independent impacts of aging on mitochondrial DNA quantity and quality in humans2017 · 182 citations
  3. 3Fatty acid binding protein 4 (FABP4) as a potential biomarker reflecting myocardial lipid storage in type 2 diabetes2019 · 62 citations
  4. 4Fetal programming of skeletal muscle development in ruminant animals12009 · 564 citations
  5. 5High Throughput Microplate Respiratory Measurements Using Minimal Quantities Of Isolated Mitochondria2011 · 500 citations