Majeed Shahnawaz, Radotra Bishan D, Sharma Sadhna
Department of Biochemistry, Postgraduate Institute of Medical Education & Research, Chandigarh, India.
Department of Histopathology, Postgraduate Institute of Medical Education & Research, Chandigarh, India.
Int J Exp Pathol. 2016 Jun;97(3):230-7. doi: 10.1111/iep.12191. Epub 2016 Jul 6.
Tuberculous meningitis (TBM) is an outcome of neuroinflammatory degeneration caused due to Mycobacterium tuberculosis infection and leads to death or neurological disabilities in the affected individuals. It causes the highest morbidity and mortality amongst all forms of tuberculosis. Matrix metalloproteinase-9 levels increase and cause inflammatory destruction during progression of the disease. Although corticosteroids are usually given as an adjuvant therapy to overcome these complications, treatment outcome is contradictory. This study was designed to evaluate whether specific inhibition of MMP-9 can be beneficial in management of the disease. MMP-9 levels were inhibited using SB-3CT or dexamethasone along with conventional drugs for treatment of tuberculous meningitis. Both SB-3CT and dexamethasone decreased the elevated levels of MMP-9 in sera and tissues of the infected mice. However, dexamethasone administration had an inhibitory effect on bacillary clearance, while SB-3CT potentiated the bacillary clearance, suggesting that MMP-9, if specifically inhibited, can be beneficial in the management of TBM.
结核性脑膜炎(TBM)是由结核分枝杆菌感染引起的神经炎性退变的结果,会导致受影响个体死亡或出现神经功能障碍。在所有形式的结核病中,它的发病率和死亡率最高。在疾病进展过程中,基质金属蛋白酶-9水平升高并导致炎症性破坏。尽管通常给予皮质类固醇作为辅助治疗以克服这些并发症,但治疗结果却相互矛盾。本研究旨在评估特异性抑制基质金属蛋白酶-9是否对该疾病的治疗有益。使用SB-3CT或地塞米松与治疗结核性脑膜炎的传统药物一起抑制基质金属蛋白酶-9水平。SB-3CT和地塞米松均降低了感染小鼠血清和组织中升高的基质金属蛋白酶-9水平。然而,地塞米松给药对细菌清除有抑制作用,而SB-3CT则增强了细菌清除,这表明如果特异性抑制基质金属蛋白酶-9,可能对结核性脑膜炎的治疗有益。