Botanical Bioflavonoid Composition from Scutellaria baicalensis- and Acacia catechu-Protected Mice against D-Galactose-Induced Immunosenescence, and Cyclophosphamide Induced Immune Suppression
Open Access
- 18 September 2024
- Vol. 16 (18) , 3144
Abstract
Oxidative stress and chronic inflammation create a perpetual cycle in the elderly, where impaired immune function amplifies susceptibility to oxidative damage, and oxidative stress further weakens the immune response. This cycle is particularly detrimental to the respiratory system of the elderly, which is an easy target for constant exogenous harmful attacks during cold/flu season or under heavy air pollution. Herbal medicines that protect respiratory function are seen as safer alternatives to conventional therapies; however, there is limited availability of scientifically validated, safe, and effective natural supplements for these conditions. In this study, we evaluated a standardized bioflavonoid composition, UP446, that contains bioactives from the roots of Scutellaria baicalensis and the heartwoods of Acacia catechu as a natural and nutritional supplement for its antioxidative and immunoregulatory effects in oxidative stress-accelerated aging and chemically induced immune suppression mouse models. Immunosenescence was induced through the repeated subcutaneous inoculation of D-galactose (D-Gal) at a dose of 500 mg/kg/day in CD-1 mice. UP446 was administered orally at doses of 100 mg/kg and 200 mg/kg starting in the fifth week of immunosenescence induction. This study lasted a total of ten weeks. All mice received a quadrivalent influenza vaccine 2 weeks before termination. Whole blood, serum, spleen homogenate, and thymus tissues were processed for analysis. Cyclophosphamide (Cy)-induced immunosuppression was triggered by three consecutive injections of cyclophosphamide at 80 mg/kg/day, followed by the oral administration of UP446 for 18 days at doses of 100 mg/kg and 200 mg/kg. Blood was collected from each animal at necropsy, and serum was isolated for IgA and IgG ELISA analysis. UP446 was found to improve immune response, as evidenced by the stimulation of innate (NK cells) and adaptive immune responses (T cells and cytotoxic T cells), an increase in antioxidant capacity (glutathione peroxidase), the preservation of vital immune organs (the thymus), and a reduction in NFκB. UP446 also increased serum levels of IgA and IgG. The findings presented in this report demonstrate the antioxidative, anti-inflammatory, and immune-regulatory activities of UP446, suggesting its potential use in respiratory conditions involving immune stress due to aging, oxidative stress, and/or pathogenic challenges.Keywords
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Funding Information
- UNIGEN
This publication has 33 references indexed in Scilit:
- Oxidative stress is the pivot for PM2.5-induced lung injuryFood and Chemical Toxicology, 2023
- Aging and aging-related diseases: from molecular mechanisms to interventions and treatmentsSignal Transduction and Targeted Therapy, 2022
- Ageing, age-related diseases and oxidative stress: What to do next?Ageing Research Reviews, 2020
- The Role of the Thymus in the Immune ResponseThoracic Surgery Clinics, 2019
- Antiviral activity of baicalin against influenza A (H1N1/H3N2) virus in cell culture and in mice and its inhibition of neuraminidaseArchives of Virology, 2014
- Inhibition of extracellular HMGB1 attenuates hyperoxia-induced inflammatory acute lung injuryRedox Biology, 2014
- Anti-influenza agents from Traditional Chinese MedicineNatural Product Reports, 2010
- 90-Day oral toxicity study of UP446, a combination of defined extracts of Scutellaria baicalensis and Acacia catechu, in ratsFood and Chemical Toxicology, 2010
- Free radical scavenging and antioxidant activities of flavonoids extracted from the radix of Scutellaria baicalensis GeorgiBiochimica et Biophysica Acta (BBA) - General Subjects, 1999
- Aging-induced Up-regulation of Nuclear Binding Activities of Oxidative Stress Responsive NF-kB Transcription Factor in Mouse Cardiac MuscleJournal of Molecular and Cellular Cardiology, 1996