PMID- 37749096 OWN - NLM STAT- MEDLINE DCOM- 20230927 LR - 20240218 IS - 2045-2322 (Electronic) IS - 2045-2322 (Linking) VI - 13 IP - 1 DP - 2023 Sep 25 TI - Zinc nanoparticles ameliorated obesity-induced cardiovascular disease: role of metabolic syndrome and iron overload. PG - 16010 LID - 10.1038/s41598-023-42550-y [doi] LID - 16010 AB - Obesity is a complicated disease characterized by abundant fat accumulation. It is associated with cardiovascular disease. The current study aimed to appreciate the role of synthesized zinc oxide nanoparticles (ZnONPs) (18.72 nm in size) in curbing cardiovascular disease in an obesity model of a high fat/sucrose diet in male rats. For 16 weeks, 24 rats were fed a high-fat diet and a 25% sucrose solution to develop obesity, and after that, the rats were randomly allocated into four groups of rats. Group 1 served as the control group and consisted of normal, non-obese rats. Group 2 comprised obese rats that were injected with an equivalent volume of a neutral substance, serving as vehicle control. In Group 3 or 4, obese rats were treated with an intraperitoneal injection of 5 or 10mg/kg of zinc oxide nanoparticles (ZnONPs) for eight weeks. The treatment of obese rats with ZnONPs decreased plasma levels of monocyte chemoattractant Protein-1 (MCP-1), resistin, ENA78, tumor necrosis factor-alpha (TNF-alpha), interleukin 6 (IL6), and C reactive protein (CRP). Also, the remediation of obese rats with ZnONPs led to a significant decrease in body mass index (BMI), body weight gain, leptin, cholesterol, triglycerides, LDL (Low-density lipoprotein), glucose, and insulin resistance index (HOMA-IR). Moreover, ZnONPs treatment lowered troponin, creatine phosphokinase-MB (CK-MB), lactate dehydrogenase (LDH), cardiac or adipose tissue iron content, and malondialdehyde (MDA) either in blood or heart tissue. Otherwise, treating obese rats with ZnONPs enhanced plasma adiponectin levels, cardiac-reduced glutathione (GSH), and superoxide dismutase (SOD). In addition, ZnONPs displayed a significant influence on the cardiovascular system since they combat the rise in blood pressure and the pathological changes of the heart and aorta besides maintaining plasma nitric oxide levels. The results showed a positive correlation between BMI and MDA, MPC-1, CK-MB, and LDH. ZnONPs are convenient in treating cardiovascular disease in obese rats via reduced blood pressure, oxidative stress, cardiac iron accumulation, insulin resistance, and inflammatory markers. CI - (c) 2023. Springer Nature Limited. FAU - Bashandy, Samir A E AU - Bashandy SAE AD - Pharmacology Department, National Research Centre, 33 El-Bohouth St., Dokki, P.O. 12622, Cairo, Egypt. FAU - El-Seidy, Ahmed M A AU - El-Seidy AMA AD - Inorganic Chemistry Department, National Research Centre, 33 El-Bohouth St., Dokki, P.O. 12622, Cairo, Egypt. FAU - Ibrahim, Fatma A A AU - Ibrahim FAA AD - Biophysics Group, Department of Biochemistry, National Research Centre, 33 El-Bohouth St., Dokki, P.O. 12622, Cairo, Egypt. FAU - Abdelrahman, Sahar S AU - Abdelrahman SS AD - Pathology Department, Faculty of Veterinary Medicine, Cairo University, Cairo, Egypt. FAU - Abdelmottaleb Moussa, Sherif A AU - Abdelmottaleb Moussa SA AD - Inorganic Chemistry Department, National Research Centre, 33 El-Bohouth St., Dokki, P.O. 12622, Cairo, Egypt. FAU - ElBaset, Marawan A AU - ElBaset MA AUID- ORCID: 0000-0002-0861-6251 AD - Pharmacology Department, National Research Centre, 33 El-Bohouth St., Dokki, P.O. 12622, Cairo, Egypt. dr.marawan@gmail.com. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20230925 PL - England TA - Sci Rep JT - Scientific reports JID - 101563288 RN - J41CSQ7QDS (Zinc) RN - SOI2LOH54Z (Zinc Oxide) RN - E1UOL152H7 (Iron) SB - IM EIN - Sci Rep. 2024 Feb 14;14(1):3746. PMID: 38355658 MH - Male MH - Animals MH - Rats MH - *Metabolic Syndrome/complications MH - Zinc MH - *Zinc Oxide MH - *Cardiovascular Diseases/etiology MH - *Insulin Resistance MH - *Metal Nanoparticles MH - Obesity/complications MH - *Iron Overload/complications/drug therapy MH - Iron PMC - PMC10519991 COIS- The authors declare no competing interests. EDAT- 2023/09/26 00:42 MHDA- 2023/09/27 06:42 PMCR- 2023/09/25 CRDT- 2023/09/25 23:17 PHST- 2023/02/18 00:00 [received] PHST- 2023/09/12 00:00 [accepted] PHST- 2023/09/27 06:42 [medline] PHST- 2023/09/26 00:42 [pubmed] PHST- 2023/09/25 23:17 [entrez] PHST- 2023/09/25 00:00 [pmc-release] AID - 10.1038/s41598-023-42550-y [pii] AID - 42550 [pii] AID - 10.1038/s41598-023-42550-y [doi] PST - epublish SO - Sci Rep. 2023 Sep 25;13(1):16010. doi: 10.1038/s41598-023-42550-y.