The effects of eight weeks of aerobic training with vitamin C on the expression pathway of antioxidants in the hippocampus tissue of TMT induced Alzheimer's disease rats.

INTRODUCTION: Alzheimer's disease (AD) is one of the most common neurological disorders and, researchers believe that the impairment of oxidant-antioxidant system plays an important role in its progression. The PI3K/NRF2 pathway has particular importance in increasing the expression of antioxidants. Thus present study aimed to investigate the effect of eight weeks of aerobic training (AT) with vitamin C (VC) on the expression pathway of antioxidants in the hippocampus tissue of trimethyltin chloride (TMT) induced Alzheimer's Disease Rats. METHODS: In this experimental study, 28 male Sprague-Dawley rats (age 14-16 months, weight 270-320 g) were injected 10 mg/kg TMT and were divided into (1) TMT (n = 7), (2) TMT + VC (n = 7), (3) TMT + AT (n = 7) and (4) TMT + VC + AT (n = 7) groups. Also, 7 healthy rats without any intervention selected as healthy control (HC) group to investigate the effects of TMT on research variables. Groups 3 and 4 ran on the treadmill for eight weeks, for 15-48 min at a speed of 10-24 m/min. Also, groups 2 and 4 received 4 mg/kg VC orally. To measure PI3K, Nrf2, SOD and catalase in the hippocampus tissue of rats, ELISA method were used. To analyze the data, one-way analysis of variance with Tukey's post- hoc tests were used (P ≤ 0.05). RESULTS: The hippocampal values of Nrf2 and SOD in TMT + VC, TMT + AT and TMT + VC + AT groups were higher than TMT group (P = 0.001). Catalase in TMT + AT and TMT + VC + AT groups was higher than TMT group (P = 0.001). Also, catalase and PI3K were higher in the TMT + VC + AT group than the TMT + VC group (P = 0.05). PI3K levels of TMT + VC + AT group were higher than TMT + AT group (P = 0.02). CONCLUSION: It seems that AT and VC, both alone and in combination, play a role in improving the transcription pathway of antioxidants in the hippocampus tissue of TMT induced Alzheimer's disease Rats. Therefore, the combination of these two interventions is suggested to improve the antioxidant system.

Evaluation of respiratory complications in patients with X-linked and autosomal recessive agammaglobulinemia.

BACKGROUND: Congenital agammaglobulinemia is the first primary immunodeficiency disorder characterized by a defect in B lymphocyte development and subsequently decreased immunoglobulin levels. These patients are prone to suffer from recurrent infections mostly involving the respiratory tract. In this study, we aimed to describe in detail respiratory tract complications as the most prominent clinical feature among agammaglobulinemic patients. METHODS: A total number of 115 patients were included. Demographic, clinical, and genetic data were collected from the patients' medical records. Among the available patients, pulmonary function tests (PFTs) and/or high-resolution computed tomography (HRCT) were performed. RESULTS: Respiratory tract complications (85.2%) especially pneumonia (62.6%) were the most prominent clinical features in our cohort. Among patients with abnormal PFT results (N = 19), a mixed respiratory pattern was observed in 36.8%. HRCT was carried out in 29 patients; Bhalla scoring-based evaluation of these patients indicated excellent (44.8%), followed by good (34.5%) and mild (20.7%) results. Bronchiectasis was found in 13 patients undergoing HRCT (44.8%). We found significant inverse correlations between the Bhalla score and incidence rate of pneumonia, as well as the presence of bronchiectasis. Patients with abnormal PFT results had statistically significant higher bronchiectasis frequency and lower Bhalla scores compared to those with normal results. Forty-one patients were deceased, and here, respiratory failure was the most common cause of death (45.5%). CONCLUSION: High prevalence of respiratory tract infections among agammaglobulinemic patients and subsequent progression to permanent lung damage highlights the importance of implementing respiratory evaluation as part of routine follow-up program of agammaglobulinemic patients. Physicians should be aware of this and regularly monitor the respiratory function of these patients to allow for timely diagnosis and treatment initiation aiming to improve patients' prognosis and quality of life.