Cardioprotective role of phoenixin-14 in isoproterenol-induced myocardial injury: Involvement of AMPK, JAK2/STAT3, and Sema3E pathways

dc.contributor.authorAkcilar, Raziye
dc.contributor.authorTasar, Muhammed
dc.contributor.authorKar, Fatih
dc.contributor.authorAri, Neziha Senem
dc.contributor.authorSaygili, Suna Karadeniz
dc.contributor.authorKocak, Fatma Emel
dc.contributor.authorKocak, Cengiz
dc.date.accessioned2025-11-16T19:33:49Z
dc.date.issued2025
dc.departmentİstanbul Medeniyet Üniversitesi
dc.description.abstractAims: This study aimed to evaluate the cardioprotective effects of phoenixin-14 (PNX-14) in isoproterenol (ISO)-induced myocardial infarction (MI) in rats, comparing both preventive and therapeutic administration. Materials and methods: Seventy adult male Wistar rats were divided into five groups: Control, PNX-14, ISO, ISO + PNX-14 (PNX-14 treatment after ISO), and PNX-14 + ISO (PNX-14 pretreatment before ISO). MI was induced by subcutaneous ISO (100 mg/kg/day) for two days. PNX-14 (5 nmol/kg, intraperitoneally) was administered once daily for 3 days. Biochemical, molecular, and histopathological analyses were performed to evaluate oxidative stress, inflammatory response, and apoptosis in cardiac tissue. Key findings: PNX-14 treatment significantly reduced the ISO-induced increases in heart/body weight ratio (0.54 +/- 0.05), infarct size (47.3 +/- 2.51 %), apoptotic index (40.8 +/- 2.99 %), and cardiac necrosis markers CK-MB and TnI (p < 0.001). It improved antioxidant defenses by increasing glutathione (GSH) and total antioxidant status (TAS), while reducing total oxidant status (TOS) and oxidative stress index (OSI). Pro-inflammatory cytokines TNF-alpha and IL-6 were lowered, and anti-inflammatory IL-10 increased. PNX-14 also attenuated apoptosis in cardiac tissue by downregulating cytochrome c, APAF-1, caspase-3, and Bax, and upregulating the anti-apoptotic marker Bcl-2. These effects were linked to modulation of Gpr173, AMPK/Nrf2/HO-1, and Sema3E/PlexinD1 pathways, alongside suppression of JAK2/STAT3 and NF-kappa B signaling. Furthermore, PNX-14 improved hemodynamic stability and histopathologically reduced ISO-induced myocardial damage. Significance: These results demonstrate that PNX-14, particularly when administered after injury, effectively attenuates myocardial damage through multi-pathway regulation of oxidative stress, inflammation, and apoptosis. PNX-14 may hold therapeutic potential for the prevention and treatment of cardiovascular diseases.
dc.description.sponsorshipTurkish Health Institutes Presidency [28557, 2022-A3-DR/TUS-03 A]
dc.description.sponsorshipThis project was supported by the Turkish Health Institutes Presidency under project number 28557, within the scope of the 2022-A3-DR/TUS-03 A Group Projects Support Program.
dc.identifier.doi10.1016/j.lfs.2025.123896
dc.identifier.issn0024-3205
dc.identifier.issn1879-0631
dc.identifier.pmid40816502
dc.identifier.scopus2-s2.0-105013114174
dc.identifier.scopusqualityQ1
dc.identifier.urihttps://doi.org/10.1016/j.lfs.2025.123896
dc.identifier.urihttps://hdl.handle.net/20.500.14730/15145
dc.identifier.volume379
dc.identifier.wosWOS:001554317800003
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherPergamon-Elsevier Science Ltd
dc.relation.ispartofLife Sciences
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WOS_20250302
dc.subjectPhoenixin 14
dc.subjectMyocardial infarction
dc.subjectOxidative stress
dc.subjectInflammation
dc.subjectApoptosis
dc.titleCardioprotective role of phoenixin-14 in isoproterenol-induced myocardial injury: Involvement of AMPK, JAK2/STAT3, and Sema3E pathways
dc.typeArticle

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