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When bones meet blood vessels: BMP-2 expression and vascular calcification in a rat model of metabolic syndrome

Heart Science Journal · Vol. 7 No. 2 (2026) · hlm. 91–98

DOI
10.21776/ub.hsj.2026.007.02.14
ISSN
2721-9984, 2721-9976
Terbit
2026-04-26
Penerbit
Universitas Brawijaya
Bahasa
en
Lisensi
creativecommons.org/licenses/by/4.0

Abstrak

Background: Vascular calcification (VC) is a significant contributor to cardiovascular morbidity, particularly in conditions like metabolic syndrome (MetS). Bone Morphogenetic Protein-2 (BMP-2) is implicated in the osteogenic differentiation of vascular cells, potentially linking MetS to VC. Objective: This study aimed to investigate aortic BMP-2 expression and the presence of VC in a rat model of MetS and assess the effects of Metformin, Empagliflozin, and a green tea/green coffee extract combination. Methods: Male Sprague-Dawley rats were induced with MetS using a high-fat, high-sucrose diet combined with a low-dose streptozotocin injection (30 mg/kgBW). Rats were divided into five groups (n=5): Normal control (NORM), MetS (METS), MetS + Metformin (MFN, 500 mg/kgBW), MetS + Empagliflozin (EMP, 30 mg/kgBW), and MetS + GTCE (300 mg/kgBW green tea + 200 mg/kgBW green coffee). Treatments were administered daily via oral gavage for 9 weeks. Result: Aortic tissue was collected for histological analysis and qRT-PCR to measure relative BMP-2 mRNA expression. Histological analysis revealed calcification in the aortic wall of the METS group rats. Compared to the NORM group, BMP-2 mRNA expression was significantly upregulated in the METS group (p<0.001). Treatment with MFN, EMP, and GTCE significantly downregulated BMP-2 mRNA expression compared to the METS group (p<0.001 for all). Conclusion: This study demonstrates that MetS induction in this rat model might promotes aortic calcification and significantly increases BMP-2 mRNA expression. Pharmacological interventions with Metformin, Empagliflozin, and green tea/coffee extract attenuated the MetS-induced upregulation of BMP-2 expression. These findings suggest a potential role for BMP-2 in MetS-associated vascular changes.

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  • University of Brawijaya
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Rekan penulisOrganisasiArtikel bersama
Mohammad Saifur RohmanUniversity of Brawijaya44
Anna Fuji RahimahUniversity of Brawijaya26
Novi KurnianingsihUniversity of Brawijaya25
Setyasih AnjarwaniUniversity of Brawijaya23
Indra PrasetyaUniversity of Brawijaya21
Sasmojo WiditoUniversity of Brawijaya20
Cholid Tri TjahjonoUniversity of Brawijaya20
Heny MartiniUniversity of Brawijaya11
Yoga WaranugrahaUniversity of Brawijaya8
Wella KarolinaUniversity of Brawijaya5
Muhammad Rizki FadlanUniversity of Brawijaya5
Putri Annisa KamilaUniversity of Brawijaya5
Adhika Prastya WikanandaUniversity of Brawijaya4
Olivia HandayaniUniversity of Brawijaya4
Anna Fuji RahimahAfiliasi tidak diketahui4
Valerinna Yogibuana Swastika PutriUniversity of Brawijaya4
Shalahuddin Suryo BaskoroUniversity of Brawijaya4
Icmi Dian RochmawatiUniversity of Brawijaya3
Dadang HendrawanUniversity of Brawijaya3
Dea Arie KurniawanUniversity of Brawijaya3
Anita Surya SantosoAfiliasi tidak diketahui3
Harris KristantoUniversity of Brawijaya3
Valerinna YogibuanaAfiliasi tidak diketahui3
Teguh AryanugrahaUniversity of Brawijaya3
Nikhen NoverikeUniversity of Brawijaya3
Taufieq Ridlo MakhmudUniversity of Brawijaya3
Faris Wahyu NugrohoUniversity of Brawijaya3
Imam Mi'raj SuprayogaUniversity of Brawijaya3
Puspa LestariUniversity of Brawijaya2
Fahmy RusnantaUniversity of Brawijaya2
Fitranti Suciati LaitupaUniversity of Brawijaya2
Tri AstiawatiUniversity of Brawijaya2
Seprian WidasmaraUniversity of Brawijaya2
Ayu Asri Devi AdityawatiUniversity of Brawijaya2
Yudi Putra ApridityaUniversity of Brawijaya2

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Sumber metadata: OAI-PMH (metadata jurnal) https://heartscience.ub.ac.id/index.php/heartscience/oai, pertama di-harvest 8 Nov 2026, terakhir terlihat 8 Nov 2026.
Metadata asli (oai_dc)
<oai_dc:dc xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/  http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
	<dc:title xml:lang="en">When bones meet blood vessels: BMP-2 expression and vascular calcification in a rat model of metabolic syndrome</dc:title>
	<dc:creator xml:lang="en">Sihotang, Fransiska Anggreni</dc:creator>
	<dc:creator xml:lang="en">Rohman, Muhammad Saifur</dc:creator>
	<dc:creator xml:lang="en">Satrijo, Budi</dc:creator>
	<dc:creator xml:lang="en">Sargowo, Djanggan</dc:creator>
	<dc:creator xml:lang="en">Rizal, Ardian </dc:creator>
	<dc:subject xml:lang="en">vascular calcification</dc:subject>
	<dc:subject xml:lang="en">metabolic syndrome</dc:subject>
	<dc:subject xml:lang="en">bone morphogenetic protein</dc:subject>
	<dc:subject xml:lang="en">metformin</dc:subject>
	<dc:subject xml:lang="en">empagliflozin</dc:subject>
	<dc:subject xml:lang="en">green tea green coffee extract</dc:subject>
	<dc:description xml:lang="en">Background: Vascular calcification (VC) is a significant contributor to cardiovascular morbidity, particularly in conditions like metabolic syndrome (MetS). Bone Morphogenetic Protein-2 (BMP-2) is implicated in the osteogenic differentiation of vascular cells, potentially linking MetS to VC.
Objective: This study aimed to investigate aortic BMP-2 expression and the presence of VC in a rat model of MetS and assess the effects of Metformin, Empagliflozin, and a green tea/green coffee extract combination.
Methods: Male Sprague-Dawley rats were induced with MetS using a high-fat, high-sucrose diet combined with a low-dose streptozotocin injection (30 mg/kgBW). Rats were divided into five groups (n=5): Normal control (NORM), MetS (METS), MetS + Metformin (MFN, 500 mg/kgBW), MetS + Empagliflozin (EMP, 30 mg/kgBW), and MetS + GTCE (300 mg/kgBW green tea + 200 mg/kgBW green coffee). Treatments were administered daily via oral gavage for 9 weeks.
Result: Aortic tissue was collected for histological analysis and qRT-PCR to measure relative BMP-2 mRNA expression. Histological analysis revealed calcification in the aortic wall of the METS group rats. Compared to the NORM group, BMP-2 mRNA expression was significantly upregulated in the METS group (p&amp;lt;0.001). Treatment with MFN, EMP, and GTCE significantly downregulated BMP-2 mRNA expression compared to the METS group (p&amp;lt;0.001 for all).
Conclusion: This study demonstrates that MetS induction in this rat model might promotes aortic calcification and significantly increases BMP-2 mRNA expression. Pharmacological interventions with Metformin, Empagliflozin, and green tea/coffee extract attenuated the MetS-induced upregulation of BMP-2 expression. These findings suggest a potential role for BMP-2 in MetS-associated vascular changes.</dc:description>
	<dc:publisher xml:lang="en">Universitas Brawijaya</dc:publisher>
	<dc:date>2026-04-26</dc:date>
	<dc:type>info:eu-repo/semantics/article</dc:type>
	<dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
	<dc:format>application/pdf</dc:format>
	<dc:identifier>https://heartscience.ub.ac.id/index.php/heartscience/article/view/20405</dc:identifier>
	<dc:identifier>10.21776/ub.hsj.2026.007.02.14</dc:identifier>
	<dc:source xml:lang="en">Heart Science Journal; Vol. 7 No. 2 (2026): The Evolving Landscape of Heart Failure; 91-98</dc:source>
	<dc:source>2721-9984</dc:source>
	<dc:source>2721-9976</dc:source>
	<dc:source>10.21776/ub.hsj.2026.007.02</dc:source>
	<dc:language>en</dc:language>
	<dc:relation>https://heartscience.ub.ac.id/index.php/heartscience/article/view/20405/585</dc:relation>
	<dc:rights xml:lang="en">Copyright (c) 2026 Fransiska Anggreni Sihotang, M Saifur Rohman, Budi Satrijo, Djanggan Sargowo, Ardian  Rizal</dc:rights>
	<dc:rights xml:lang="en">http://creativecommons.org/licenses/by/4.0</dc:rights>
</oai_dc:dc>