Effects of sodium salicylate and time postpartum on mammary tissue proliferation, gene transcript profile, and DNA methylation.


Journal

Journal of dairy science
ISSN: 1525-3198
Titre abrégé: J Dairy Sci
Pays: United States
ID NLM: 2985126R

Informations de publication

Date de publication:
Oct 2021
Historique:
received: 30 12 2020
accepted: 12 05 2021
pubmed: 27 7 2021
medline: 24 9 2021
entrez: 26 7 2021
Statut: ppublish

Résumé

Previous studies have demonstrated nonsteroidal antiinflammatory drug treatment in early lactation had a positive impact on whole-lactation milk production in older cows. The objective of this study was to evaluate proliferative, transcriptional, and epigenetic changes in the mammary gland that could explain increased production responses due to nonsteroidal antiinflammatory drug treatment. Sodium salicylate (SAL; 125 g/d) or water (CON) were administered via oral drench to multiparous Holstein cows (n = 8/treatment) once daily for 3 d beginning approximately 24 h after parturition, and mammary tissue was collected on d 1, 4, and 45 postpartum. Day 1 tissue was collected immediately preceding the initial drench, and d 4 tissue was collected 24 h following the final drench. Blood was collected twice weekly and analyzed for plasma glucose, insulin, β-hydroxybutyrate, free fatty acids, and prolactin. Cows were milked twice daily until d 7 of lactation, and thrice daily for the remainder of the study. Total RNA extracted from tissue was deep-sequenced and analyzed for differential gene expression using DESeq2. We detected no treatment effect on milk yield or plasma metabolites through 45 d of lactation; additionally, no change in mammary epithelial cell proliferation was detected when assessed by Ki67 labeling. Comparison of SAL versus CON revealed that only 16 of 18,286 genes were differentially expressed (false discovery rate <0.1) in mammary tissue collected on d 45, whereas no differentially expressed genes due to treatment were detected on d 1 or 4. Analysis of transcriptional differences over time showed downregulation of pathways related to immune cell recruitment and differentiation, and extensive overlap with pathways related to cholesterol synthesis and liver X receptor signaling. Global DNA methylation of mammary tissue was decreased for CON compared with SAL. Transcriptome analysis emphasized extensive involvement of immune-related signaling pathways in the switch from lactogenesis to galactopoiesis, and changes in methylation with SAL treatment merit future investigation into epigenetic effects on milk production.

Identifiants

pubmed: 34304880
pii: S0022-0302(21)00753-0
doi: 10.3168/jds.2020-20109
pii:
doi:

Substances chimiques

Sodium Salicylate WIQ1H85SYP

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

11259-11276

Informations de copyright

© 2021, The Authors. Published by Elsevier Inc. and Fass Inc. on behalf of the American Dairy Science Association®. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

Auteurs

C M Ylioja (CM)

Department of Animal Sciences and Industry, Kansas State University, Manhattan 66506.

A J Carpenter (AJ)

Department of Animal Sciences and Industry, Kansas State University, Manhattan 66506.

L K Mamedova (LK)

Department of Animal Sciences and Industry, Kansas State University, Manhattan 66506; Department of Animal Science, Michigan State University, East Lansing 48824.

K M Daniels (KM)

Department of Dairy Science, Virginia Tech, Blacksburg 24061.

P J Ross (PJ)

Department of Animal Science, University of California, Davis 95616.

S L Laflin (SL)

Department of Clinical Sciences, Kansas State University, Manhattan 66506.

T H Swartz (TH)

Department of Animal Sciences and Industry, Kansas State University, Manhattan 66506; Department of Animal Science, Michigan State University, East Lansing 48824.

B J Bradford (BJ)

Department of Animal Sciences and Industry, Kansas State University, Manhattan 66506; Department of Animal Science, Michigan State University, East Lansing 48824. Electronic address: bjbrad@msu.edu.

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