Evidence map›Paper›PMID 25933189›Full record

ArticlePloS one2015

Protection against T1DM-Induced Bone Loss by Zinc Supplementation: Biomechanical, Histomorphometric, and Molecular Analyses in STZ-Induced Diabetic Rats.

Raul Hernandes Bortolin, Bento João da Graça Azevedo Abreu, Marcela Abbott Galvão Ururahy, Karla Simone Costa de Souza, João Felipe Bezerra, Melina Bezerra Loureiro, Flávio Santos da Silva, Dáfiny Emanuele da Silva Marques, Angélica Amanda de Sousa Batista, Gisele Oliveira and 7 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
5.9field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 50 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Exploring the Potential ofInternational journal of medical sciences · 2025
    Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Zinc as a Therapeutic Agent in Bone Regeneration.Materials (Basel, Switzerland) · 2020
    Review
  16. Article
  17. Journal of molecular endocrinology · 2017
    Article
  18. Review
  19. Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors at 4 institutions in 1 country.

Raul Hernandes BortolinDepartment of Clinical and Toxicological Analyses, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil.
Bento João da Graça Azevedo AbreuDepartment of Morphology, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil.
Marcela Abbott Galvão UrurahyDepartment of Clinical and Toxicological Analyses, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil.
Karla Simone Costa de SouzaDepartment of Clinical and Toxicological Analyses, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil.
João Felipe BezerraDepartment of Clinical and Toxicological Analyses, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil.
Melina Bezerra LoureiroDepartment of Clinical and Toxicological Analyses, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil.
Flávio Santos da SilvaDepartment of Morphology, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil.
Dáfiny Emanuele da Silva MarquesDepartment of Morphology, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil.
Angélica Amanda de Sousa BatistaDepartment of Chemistry, University of Ribeirão Preto, Ribeirão Preto, São Paulo, Brazil.
Gisele OliveiraDepartment of Chemistry, University of Ribeirão Preto, Ribeirão Preto, São Paulo, Brazil.
André Ducati LuchessiDepartment of Clinical and Toxicological Analyses, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil.
Valéria Morgiana Gualberto Duarte Moreira LimaDepartment of Pharmacy, State University of Paraiba, Campina Grande, Paraiba, Brazil.
Carlos Eduardo Saraiva MirandaDepartment of Pharmacy, University of Ribeirão Preto, Ribeirão Preto, São Paulo, Brazil.
Marcus Vinicius Lia FookLaboratory of Evaluation and Development of Biomaterials, Federal University of Campina Grande, Campina Grande, Paraiba, Brazil.
Maria das Graças AlmeidaDepartment of Clinical and Toxicological Analyses, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil.
Luciana Augusto de RezendeDepartment of Chemistry, University of Ribeirão Preto, Ribeirão Preto, São Paulo, Brazil.
Adriana Augusto de RezendeDepartment of Clinical and Toxicological Analyses, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil.
Universidade Federal do Rio Grande do Norte · BRUniversidade de Ribeirão Preto · BRUniversidade Estadual da Paraíba · BRUniversidade Federal de Campina Grande · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several studies have established an association between diabetes and alterations in bone metabolism; however, the underlying mechanism is not well established. Although zinc is recognized as a potential preventive agent against diabetes-induced bone loss, there is no evidence demonstrating its effect in chronic diabetic conditions. This study evaluated the effects of zinc supplementation in a chronic (90 days) type 1 diabetes-induced bone-loss model. Male Wistar rats were distributed in three groups: control, type 1 diabetes mellitus (T1DM), and T1DM plus zinc supplementation (T1DMS). Serum biochemical analysis; tibia histomorphometric, biomechanical, and collagen-content analyses; and femur mRNA expression were evaluated. Relative to T1DM, the zinc-supplemented group showed increased histomorphometric parameters such as TbWi and BAr and decreased TbSp, increased biomechanical parameters (maximum load, stiffness, ultimate strain, and Young's modulus), and increased type I collagen content. Interestingly, similar values for these parameters were observed between the T1DMS and control groups. These results demonstrate the protective effect of zinc on the maintenance of bone strength and flexibility. In addition, downregulation of OPG, COL1A, and MMP-9 genes was observed in T1DMS, and the anabolic effects of zinc were evidenced by increased OC expression and serum ALP activity, both related to osteoblastogenesis, demonstrating a positive effect on bone formation. In contrast, T1DM showed excessive bone loss, observed through reduced histomorphometric and biomechanical parameters, characterizing diabetes-associated bone loss. The bone loss was also observed through upregulation of OPG, COL1A, and MMP-9 genes. In conclusion, zinc showed a positive effect on the maintenance of bone architecture and biomechanical parameters. Indeed, OC upregulation and control of expression of OPG, COL1A, and MMP-9 mRNAs, even in chronic hyperglycemia, support an anabolic and protective effect of zinc under chronic diabetic conditions. Furthermore, these results indicate that zinc supplementation could act as a complementary therapy in chronic T1DM.

Indexed as

Dietary SupplementsAnimalsBiomechanical PhenomenaBone DensityBone ResorptionCollagen Type ICollagen Type I, alpha 1 ChainDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 1Elastic ModulusFemurGene Expression RegulationHumansMaleMatrix Metalloproteinase 9OsteocalcinCollagen Type ICollagen Type I, alpha 1 ChainMatrix Metalloproteinase 9OsteocalcinOsteoprotegerinRNA, MessengerStreptozocinTnfrsf11b protein, ratZinc

Identifiers

PMID25933189
PMCPMC4416905
OpenAlexW1582849500

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.