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JDRS · Open access journal

Original Article · Open access

Potential preventive effects of angiotensin-(1-7) on bone matrix quality in diabetic rats through modulation of the organic matrix

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Ugur Dalaman

Department of Biophysics, Afyonkarahisar Health Sciences University School of Medicine, Afyonkarahisar, Türkiye

ORCID: 0000-0001-7145-4139

Ibrahim Cuneyit

Department of Anatomy, Pamukkale University, School of Medicine, Denizli, Türkiye

ORCID: 0000-0003-0555-2114

Şevval Öztürk

Department of Anatomy, Pamukkale University, School of Medicine, Denizli, Türkiye

ORCID: 0000-0001-7189-4257

Ege Rıza Karagur

Department of Medical Genetics, Pamukkale University, School of Medicine, Denizli, Türkiye

ORCID: 0000-0003-2189-8553

Mert Ocak

Department of Anatomy, Ankara University, School of Dentistry, Ankara, Türkiye

ORCID: 0000-0001-6832-6208

Nazmi Yaras

Department of Biophysics, Akdeniz University, School of Medicine, Antalya, Türkiye

ORCID: 0000-0002-9450-2698

Mustafa Unal

Department of Orthopaedic Surgery, Harvard Medical School, Boston, United States

ORCID: 0000-0002-9518-8952

Baris Ozgur Donmez

Department of Mechanical Engineering, Purdue University, College of Engineering, Indianapolis, United States

ORCID: 0000-0003-1066-5981

Abstract

Objectives: This experimental study aims to investigate the effects of angiotensin (1-7) (Ang-[1-7]) on the microstructural, biomechanical, and biophysicochemical properties of bone tissue in diabetic rats.

Materials and methods: Forty-eight male Wistar rats, aged three months and weighing between 280 and 330 g, were used in this study. Four groups, each containing 12 rats, were established: Control, diabetes mellitus (DM), DM-Ang-(1-7), and Ang-(1-7). The samples underwent analysis through micro-computed tomography (CT), Raman spectroscopy, and three-point bending biomechanical test.

Results: Diabetes significantly impaired bone quality, with reduced cortical thickness, maximum load, and flexural strength (p<0.05). The Ang-(1-7) treatment improved flexural strength (p<0.05), but did not fully restore mechanical function. Micro-CT showed decreased bone volume and trabecular thickness in both diabetic groups (p<0.05), with no significant recovery by Ang-(1-7). Raman spectroscopy revealed lower mineral-to-matrix ratio and disrupted collagen quality in diabetic bone (p<0.05), while Ang-(1-7) partially restored collagen-related parameters.

Conclusion: These findings highlight that Ang-(1-7) has minimal impact on bone minerals in DM rats. However, it may have a potential preventive effect on the triple-helix structural impairment within the bone organic matrix in this model.

Declarations

Author Contributions

Conceptualization, methodology: U.D., M.U.; Writing-review and editing: U.D., M.U., B.O.D., E.R.K, N.Y.; Visualization: U.D., E.R.K., M.U.; Formal analysis: M.O., M.U.; Resources: B.O.D.; Project administration: N.Y. All authors have contributed to the investigation. All authors read and approved the final manuscript.

Conflict of Interest

The authors declared no conflicts of interest with respect to the authorship and/or publication of this article.

Financial Disclosure

The authors received no financial support for the research and/or authorship of this article.

Data Sharing Statement

The data that support the findings of this study are available from the corresponding author upon reasonable request.