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. 2025 May;398(5):5845-5865.
doi: 10.1007/s00210-024-03659-7. Epub 2024 Nov 30.

Potential therapeutic and ameliorative effects of ramipril alone and in combination with methylprednisolone for the cytokine releasing syndrome in mice: An in vivo study

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Potential therapeutic and ameliorative effects of ramipril alone and in combination with methylprednisolone for the cytokine releasing syndrome in mice: An in vivo study

Marwa Salih Al-Naimi et al. Naunyn Schmiedebergs Arch Pharmacol. 2025 May.

Abstract

Cytokine-releasing syndrome (CRS) is a special form of systemic inflammatory response syndrome provoked by factors like viral infections and certain immunomodulatory drugs like monoclonal antibodies and adoptive T therapy. To elucidate the potential role of ramipril (RM) and its combination with methylprednisolone (MP) against the development and progression of CRS in mice. This experiment consists of two parts: protective and therapeutic interventions. The protective experiment: in the induction group, mice received an intraperitoneal injection (IP) of 5mg/kg lipopolysaccharide (LPS) without intervention. The other groups received various drugs before the induction by three days, then observed for an additional two days (50 mg/kg MP, 3 mg/kg RM, and a combination of 1.5 mg/kg RM with 25 mg/kg MP). The second part of the study involves the therapeutic potential; all groups received similar doses of drugs in the prevention groups, except LPS induction was given first, and after one hour, the mice received daily doses of the drugs for five days. At the end of the experiment, blood and tissue samples were obtained. Mice treated with RM and its combination with MP showed improved serum TNF-α, IL-6, IL-8, IL-1β, INF-γ, MDA, and GSH in both prevention and therapeutic groups. Histopathologically, mice treated with ramipril and its combination with MP ameliorate the tissue damage in both lung and liver tissues following LPS induction. Ramipril showed protective and therapeutic effects in LPS-induced cytokine storms in mice through anti-inflammatory and antioxidant mechanisms.

Keywords: Angiotensin-converting enzyme; Antioxidant; Cytokine storm; Inflammation.

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Conflict of interest statement

Declarations. Ethics approval: The study was approved by the Research Ethical Committee of the College of Medicine, Al-Nahrain University, approval number (UNCOMIRB34902024), data (4 December 2022), following the American Veterinary Association Guidelines (AVMA) (Underwood and Anthony 2020). Consent to participate: Not applicable. Competing interests: The authors declare no competing interests.

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