Naringin exhibits adaptogen-like and neuroprotective effects on mice under chronic stress, reversing cortical neuroinflammation and neurodegeneration

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Authors: Vivian O. Ojiakor, Benneth Ben-Azu, Elizabeth Finbarrs-Bello, Emmanuel Esom, Chike Anibeze, Emeka G. Anyanwu
Cited by: 3
References: 89

Abstract

Chronic unpredictable mild stress (CUMS) induces impairment in cortical functional connectivity, which plays an important role in depression and anxiety. It remains unclear if naringin, a natural adaptogen with antidepressant and anxiolytic effects, reverses CUMS-induced depression by normalizing cortical dysfunction. Therefore, this study investigated the adaptogen-like anti-anxiety and antidepressant effects of naringin on mice subjected to CUMS and the underlying mechanisms in the prefrontal cortex (PFC). Adult male Swiss mice (n=9/group) received daily intraperitoneal injections of saline (10 mL/kg) for control and CUMS, naringin (2.5, 5, and 10mg/kg), or fluoxetine (10mg/kg), enduring CUMS for 21 days. Mice were assessed for depression and anxiety via neurobehavioural tests and neurochemical, biochemical and histochemical evaluations in the PFC. The hypothalamic-pituitary-adrenal (HPA) axis was measured by adrenal weight, serum corticosterone, and glucose levels. Naringin treatment reduced CUMS-induced depression, evidenced by higher sucrose consumption and decreased immobility in tests. It also alleviated anxiety-like behaviors in the elevated-plus maze and open-field tests. These effects correlated with lower corticosterone, serum glucose, and adrenal gland size. Naringin increased cortical antioxidant levels while reducing CUMS-induced lipid/nitrergic peroxidation and TNF-α and IL-1β. Both naringin and fluoxetine boosted serotonin, dopamine, and norepinephrine release in the PFC. Additionally, naringin countered CUMS-induced astrogliosis by lowering glial fibrillary acidic protein and upregulating brain-derived neurotrophic factor, with reduced pyknosis in the PFC. Naringin’s antidepressant/anxiolytic effects stem from inhibiting inflammation, oxidative stress, enhancing HPA function, monoamine release, and astrocytic activity in the mouse PFC. • NAR abated CUMS-induced depression and anxiety • NAR’s antidepressant effect involves improved cortical antioxidant system • NAR’s antidepressant effect involves inhibition cortical neuroinflammation • NAR countered CUMS-induced cortical astrogliosis • NAR improved cortical neurogenesis and neurotropism in CUMS mice

Fields of Study & Subjects

Tryptophan and brain disorders Stress Responses and Cortisol Inflammasome and immune disorders

Publication details

Journal / source
European Journal of Medicinal Chemistry Reports
Publisher
Elsevier BV
Volume
16
Pages
100323–100323
Publication date
15 January 2026
Language
EN