Morin Augmented Myocardial eNOS/cGMP/PKG Signaling Pathway and Abated Oxidative and Inflammo-apoptotic Responses in Diethyl Phthalate and Bisphenol-S Co-Exposed Male Albino Rats

• Published in: Inflammation 2023-02, Vol.46 (1), p.175-189
• Main Authors: James, Adewale Segun, Eteng, Ofem Effiom, Dosumu, Oluwatosin Adebisi, Moses, Ceasar Antiya, Ogbonna, Chukwuka Uzoamaka, Adeleye, Oladokun Abdulwasiu, Ugwor, Emmanuel Ifeanyichukwu, Omilo, Blessing Chukwueku, Fabunmi, Risikat Funmilayo, Olakitan, Aduragbemi Moses, Ugbaja, Regina Ngozi
• Format: Article
• Language: English
• Subjects: Androgen receptors; Animals; Antioxidants - metabolism; Antioxidants - pharmacology; Antioxidants - therapeutic use; Apoptosis; Arginase; Bax protein; Biomedical and Life Sciences; Biomedicine; Catalase; Cytokines; Diethyl phthalate; Dimethyl sulfoxide; Dimethyl Sulfoxide - pharmacology; DNA damage; DNA fragmentation; Flavonoids; Flavonoids - pharmacology; Flavonoids - therapeutic use; Gene expression; Glutathione peroxidase; Heart; Hydrogen peroxide; Hydrogen Peroxide - pharmacology; Immunology; Interleukin 10; Internal Medicine; Male; NF-κB protein; Nitric oxide; Original Article; Oxidative Stress; Pathology; Pharmacology/Toxicology; Rats; Rats, Wistar; Rheumatology; Signal Transduction; Tumor necrosis factor-α; Vascular endothelial growth factor; Vascular Endothelial Growth Factor A - metabolism
• ISSN: 0360-3997; 1573-2576
• DOI: 10.1007/s10753-022-01720-2

Cardiac failure accounts for many deaths worldwide. Increasing experimental evidence suggests that exposure to chemicals such as bisphenol-S (BPS) and diethyl phthalate (DEP) exacerbate cardiac injuries. Morin is a flavonoid with reported cardioprotective activity. This study evaluated the modulation of pathways relevant to cardiac endothelial function in rats exposed to BPS and DEP mixture (Mix). Thirty male albino rats were distributed across five groups ( n  = 6): control received dimethyl sulfoxide (DMSO) as vehicle, Mix dissolved in DMSO, Mix + morin (25 mg/kg), Mix + morin (50 mg/kg), and morin (50 mg/kg). After 21 days of oral exposure at 1 ml/kg bodyweight of the Mix and treatment with morin, the animals were sacrificed, and their hearts were excised for biochemical, histological, immunohistochemical, and gene expression analyses. Exposure to the Mix caused a significant increase in oxidative stress indices (H 2 O 2 , malondialdehyde, DNA fragmentation, and advanced oxidation protein products). Also, arginase, phosphodiesterase 5′, and the relative expression of TNF-α, interleukin-1β, Bax, androgen receptor, and vascular endothelial growth factor were markedly increased. In contrast, nitric oxide, reduced glutathione, interleukin-10 levels, superoxide dismutase, catalase, and glutathione peroxidase activities decreased significantly. Furthermore, p-NF-kB-p65 expression increased markedly in the Mix-exposed group. Morin treatment significantly reversed these perturbations in a dose-dependent manner in most instances. This study concludes that morin might offer a cardioprotective effect by enhancing the cardiac endothelial system and attenuating oxidative stress, inflammation, and apoptosis elicited by BPS and DEP co-exposure in male Wistar rats.