Maryam Karimi, Mahtab Moazzami, Najmeh Rezaeian,
Volume 15, Issue 1 (1-2021)
Abstract
Background and objectives: Multiple sclerosis (MS) is a common debilitating neurodegenerative disease caused by inflammatory demyelinating processes in the central nervous system. The present study aimed to evaluate the effects of core stability training on serum levels of progranulin and tumor necrosis factor alpha (TNF-α) in women with MS.
Methods: The study population consisted of 24 women with MS (aged 25 to 40 years) in Bojnourd (Iran) with expanded disability status scale score of 2-5. Patients were randomly divided into two groups of core stability training (n=12) and control (n=12). The training group performed 30-40 minutes of core stability training, three sessions a week for eight weeks. Blood sampling was done 24 hours before the first session and 48 hours after the last training session. Serum levels of progranulin and TNF-α were measured using commercial ELISA kits. Analysis of covariance was used to assess data at a significance level of 0.05 .
Results: The eight-week core stability training was associated with a significant increase in serum level of progranulin (P=0.037) and a significant decrease in the level of TNF-α (P=0.000).
Conclusion: The findings indicate that the eight-week core stability training could significantly change serum levels of progranulin and TNF-α and improve the condition of women with MS. Therefore, this type of training could be applied as a complementary therapy for MS patients.
Dr Bahman Aghcheli, Alireza.tmn@gmail.com Romina Yavarinamini, Dr Alireza Tahamtan,
Volume 19, Issue 6 (11-2025)
Abstract
Introduction: Respiratory syncytial virus (RSV) is a leading cause of severe lower respiratory tract infections in infants and young children, with disease severity linked to excessive inflammation. A20 (TNFAIP3) is a negative regulator of NF‑κB signalling and may modulate RSV-induced lung inflammation. Here, we investigated the effect of RSV infection on pulmonary A20 gene expression in a murine model.
Methods: Female BALB/c mice (n=12; 6 per group) were intranasally infected with RSV (3 × 10⁶ PFU) and euthanized on day 5 post‑infection. Lung tissues were collected to analyse the A20 (TNFAIP3) mRNA expression 5 days following RSV infection by Real‑time RT‑PCR.
Results: Quantitative PCR analysis demonstrated a statistically significant upregulation of A20 expression in the lungs of RSV-infected mice compared to the uninfected control group 5 days following infection (p=0.0048).
Conclusions: RSV infection in mice induces A20 expression, suggesting a potential role for A20 in regulating pulmonary inflammation following the virus infection.