Detrusor Myocyte Autophagy Protects the Bladder Function via Inhibiting the Inflammation in Cyclophosphamide-Induced Cystitis in Rats

التفاصيل البيبلوغرافية
العنوان: Detrusor Myocyte Autophagy Protects the Bladder Function via Inhibiting the Inflammation in Cyclophosphamide-Induced Cystitis in Rats
المؤلفون: Bo Song, Qi-Xiang Song, Xinyu Bai, Longkun Li, Liang Wang, Xingyou Dong, Xingliang Yang, Margot S. Damaser, Jiang Zhao
المصدر: PLoS ONE
PLoS ONE, Vol 10, Iss 4, p e0122597 (2015)
بيانات النشر: Public Library of Science, 2015.
سنة النشر: 2015
مصطلحات موضوعية: Science, Myocytes, Smooth Muscle, Urinary Bladder, SOD2, Inflammation, Pharmacology, Biology, medicine.disease_cause, Rats, Sprague-Dawley, Malondialdehyde, Cystitis, medicine, Autophagy, Animals, Cyclophosphamide, Multidisciplinary, Urinary bladder, medicine.diagnostic_test, Superoxide Dismutase, Interleukins, Cystometry, Interstitial cystitis, Muscle, Smooth, Organ Size, medicine.disease, Glutathione, medicine.anatomical_structure, Ribosomal protein s6, Immunology, Medicine, Female, medicine.symptom, Oxidative stress, Research Article
الوصف: Autophagy, a highly conserved homeostatic cellular process that removes and recycles damaged proteins and organelles in response to cellular stress, is believed to play a crucial role in the immune response and inflammation. The role of autophagy in bladder cystitis, however, has not well been clarified. Here we investigate the role of detrusor myocytes autophagy (DMA) in cyclophosphamide-induced cystitis animal model. 164 female Sprague-Dawley rats were randomized into three experimental groups and compared to three control groups, respectively. The expressions of microtubule-associated protein 1 light chain 3 (LC3), p-p70s6k (the phosphorylated form of ribosomal protein S6), SOD2 (superoxide dismutase 2) in the bladder muscular layer were measured using western blot. The co-location of LC3, alpha-smooth muscle actin (α-SMA), and autophagic vacuoles were investigated with double-labeled immunofluorescence and transmission electron microscopy (TEM). The expression of lL-1β, IL-6, IL-8, malondialdehyde (MDA), and glutathione (GSH) in the detrusor layer were analyzed using ELISA. The bladder inflammation and the number of mast cells in the muscular layer were analyzed by histology. The bladder function was evaluated using cystometry. In cyclophosphamide-induced cystitis, autophagy was detected in detrusor myocytes by increased LC3, p-p70s6k expression, and autophagosomes. However, the presence of enhanced inflammation and oxidative stress in the cyclophosphamide-treated group suggest autophagy of detrusor myocytes may not be sufficiently activated. Inflammation and oxidative stress were significantly decreased and the bladder histology and micturition function were significantly improved with rapamycin (RAPA, autophagy agonist) pre-treatment. In contrast, inflammation and oxidative stress were dramatically increased and the bladder histology and function were negatively affected with chloroquine (CQ, autophagy blocker) pre-treated. These findings preferentially provide evidence of the association between DMA and cyclophosphamide-induced cystitis in rats. The autophagy agonist RAPA significantly decreased the inflammation and protected the bladder function, which might be considered as a potential treatment for interstitial cystitis.
اللغة: English
تدمد: 1932-6203
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11313275c8e3129c2fdcdf14cb66c8b5Test
http://europepmc.org/articles/PMC4382282Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....11313275c8e3129c2fdcdf14cb66c8b5
قاعدة البيانات: OpenAIRE