Evidence map›Paper›PMID 42613932›Full record

ArticleMolecular nutrition & food research2026

Dietary Vitamin D2 Is Less Potent Than Vitamin D3 at Maintaining or Restoring Structure and Metabolism of Skeletal Muscle and Heart in Male Rats.

Soumam Dutta, Athira Anilkumar S, Mohd Urooj, Ayesha Ismail

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Article in Molecular nutrition & food research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Soumam DuttaDepartment of Endocrinology, ICMR-National Institute of Nutrition, Hyderabad, India.
Athira Anilkumar SDepartment of Endocrinology, ICMR-National Institute of Nutrition, Hyderabad, India.
Mohd UroojDepartment of Pharmacology & Toxicology, CCRUM-National Research Institute of Unani Medicine For Skin Disorders, Hyderabad, India.
Ayesha IsmailDepartment of Endocrinology, ICMR-National Institute of Nutrition, Hyderabad, India.

Funding

Department of Biotechnology (DBT) BT/PR33124/PFN/20/1444/2019Department of Biotechnology, Ministry of Science and Technology, India
6 · The paper itself

Abstract

Vitamin D (VD) deficiency is prevalent globally. To improve dietary recommendations for food fortification, we used male rats fed with diets depleted of VD or supplemented/rehabilitated with either vitamin D2 or vitamin D3 or combination, and compared their impact on calcium homeostasis, skeletal muscle and heart. Body composition was assessed by DEXA, muscle strength by grip test. Serum calcium, parathyroid hormone and 25-hydroxyvitamin D [25(OH)D] were measured using standard methods. Skeletal muscle and left ventricle were used for histopathology; RNA and protein were extracted for analysis of gene expression and enzymatic activity, respectively. 25-hydroxylated form of D3 was significantly higher than that of D2 in serum. D2 was less efficacious than D3 at improving skeletal muscle fiber size, strength, expression of contractility genes [Myh2, Tnnc1] and metabolic enzymes [Cs, β-Had]. Under maintenance cardiac contractility gene expression [Myh7 & Serca2a] was comparable between the D2 and D3 groups, though 400 IU D2 notably suppressed Serca2 expression. Post-rehabilitation, the 2000 IU D3 group demonstrated significant improvement in these genes. Overall, our study demonstrates similar efficacy of D2 and D3 at regulating calcium homeostasis, but a better efficacy of D3 than D2 on structure, function and energy metabolism of skeletal muscle and heart.

Indexed as

CholecalciferolErgocalciferolsHeartMuscle, SkeletalMyocardiumAnimalsBody CompositionCalciumDietary SupplementsMaleMuscle StrengthMyosin Heavy ChainsParathyroid HormoneRatsRats, Sprague-DawleySarcoplasmic Reticulum Calcium-Transporting ATPasesCalciumCholecalciferolErgocalciferolsMYH7 protein, ratMyosin Heavy ChainsParathyroid HormoneSarcoplasmic Reticulum Calcium-Transporting ATPasescontractilityheartmetabolismskeletal musclevitamin D2vitamin D3

Identifiers

PMID42613932
PMCPMC13487348

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.