Repository logo
 
Publication

SGLT2 Inhibitors: Novel approach to modulate appetite hormones and cardiomyocyte function

dc.contributor.authorCorreia, Beatriz
dc.contributor.authorRodrigues, Alexandre
dc.contributor.authorAlves, Inês
dc.contributor.authorMoraña-Fernández, Sandra
dc.contributor.authorMendes, Claúdia
dc.contributor.authorMorais, Juliana
dc.contributor.authorGonçalves, Alexandre
dc.contributor.authorFalcão-Pires, Inês
dc.date.accessioned2025-05-15T13:54:30Z
dc.date.available2025-05-15T13:54:30Z
dc.date.issued2024-05
dc.description.abstractEmerging as a class of oral antidiabetic drugs, sodium-glucose cotransporter 2 inhibitors (SGLT2i), used in patients with type 2 diabetes, offer promising results in weight loss, decreasing cardiometabolic biomarkers, thus improving overall cardiac function. The aim of this study is to assess whether SGLT2i can impact food and water consumption, hormone regulating appetite mechanisms, and morphologic parameters. Thirty-nine male ZSF1 rats were divided into two lean (Ln) and two obese (Ob) groups, fed with normal diet (ND) or treated with SGLT2i in food (30 mg/Kg/day). Body weight (BW), food, water, adiponectin and leptin were measured during nine weeks of treatment. Histochemistry analysis was performed with hematoxylin and eosin to determine the cross-section area in visceral adipose tissue (VAT), subcutaneous adipose tissue (SAT), and cardiomyocytes. SGLT2i treatment promoted an increased food and water intake in lean rats (Ln_ SGLT2i). However, the BW in this group was markedly reduced compared with non-treated lean (Ln_ND). Furthermore, the treatment promoted higher water intake despite no differences in BW in obese rats (Ob_ SGLT2i) compared to control (Ob_ND). Exploring the hormone-regulating appetite mechanisms, SGLT2i treatment showed significant increased in adiponectin levels in both Ln and Ob, however leptin levels only validated the hyperleptinemia in Ob. The ratio adiponectin/leptin was markedly significant increase in Ln_ SGLT2i rats. At the endpoint, the treatment decreased perigonadal fat weight (PFW) in both groups. Aligned with these, cross-section areas of VAT, SAT and cardiomyocytes were markedly increased in Ob, and the treatment decreased these areas in Ob_ SGLT2i. SGLT2i treatment increased food and water intake as also the adiponectin/leptin ratio in Ln. Additionally, the treatment promoted PFW loss and increased the adiponectin levels in both groups and decreased the cross-section area of VAT, SAT, cardiomyocytes in Ob.por
dc.identifier.citationCorreia, B., Rodrigues, A., Alves, I., Moraña-Fernández, S., Mendes, C., Morais, J., Gonçalves, A., & Falcão-Pires, I. (2024). SGLT2 Inhibitors: Novel approach to modulate appetite hormones and cardiomyocyte function. Livro de Resumos do 17o Encontro de Investigação Jovem da U.Porto / Book of Abstracts Young Researchers Meeting of U.Porto, 351–352. https://www.up.pt/ijup/wp-content/uploads/sites/892/2024/05/Livro-de-Resumos_final.pdf
dc.identifier.isbn978-989-746-378-5
dc.identifier.urihttp://hdl.handle.net/10400.22/30078
dc.language.isoeng
dc.peerreviewedn/a
dc.publisherUniversidade do Porto
dc.relation.hasversionhttps://www.up.pt/ijup/wp-content/uploads/sites/892/2024/05/Livro-de-Resumos_final.pdf
dc.rights.uriN/A
dc.subjectSGLT2i
dc.subjectHormone regulating appetite
dc.subjectAdiponectin/Leptin ratio
dc.subjectCardiac function
dc.titleSGLT2 Inhibitors: Novel approach to modulate appetite hormones and cardiomyocyte functionpor
dc.typeconference paper
dspace.entity.typePublication
oaire.citation.conferenceDate2024-05
oaire.citation.conferencePlacePorto
oaire.citation.endPage352
oaire.citation.startPage351
oaire.citation.titleLivro de Resumos do 17.º Encontro de Investigação Jovem da U.Porto / Book of Abstracts Young Researchers Meeting of U.Porto
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85

Files

Original bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
COM_Juliana Morais.pdf
Size:
489.54 KB
Format:
Adobe Portable Document Format
License bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
4.03 KB
Format:
Item-specific license agreed upon to submission
Description: