Nanni J M, Nguyen K H, Alford C E, Robinson C P, Stewart C M, Maeda N, Humphreys-Beher M G
Department of Oral Biology, University of Florida, Gainesville, USA.
Clin Exp Rheumatol. 1997 Sep-Oct;15(5):515-21.
Bromhexine has been reported to alleviate the xerostomia and xerophthalmia associated with secondary Sjögren's syndrome. The aim of this study was to determine if it might prove useful in the treatment of Sjögren's syndrome-like disease of the NOD mouse model for autoimmune sialoadenitis.
Groups of mice were divided into sets receiving 60 mg/kg bromhexine in drinking water and control pair-fed animals. The efficacy of drug treatment was assessed by weekly measurement of stimulated saliva volumes, protein concentration, and amylase activity. At termination (20 weeks) submandibular and lacrimal glands were removed to assess the levels of lymphocytic infiltration by histological evaluation under light microscopy.
Control and bromhexine-treated groups of mice showed no difference in the loss or rate of reduction in stimulated saliva flow over the 12 weeks of treatment. No differences were noted in the protein concentration and amylase loss with increasing age of the animals. Similar temporal changes in total protein profiles and aberrant expression of the 20 kDa parotid secretory protein isoform were observed by SDS-polyacrylamide gel profiles and Western bolt analysis. Histological evaluation of exocrine gland sections failed to detect any reduction in focal lymphocyte infiltration.
Bromhexine therapy did not alter the development or severity of Sjögren's syndrome-like disease in the NOD mouse model for autoimmune sialoadenitis.
据报道,氨溴索可缓解与继发性干燥综合征相关的口干症和干眼症。本研究的目的是确定其是否可能对自身免疫性涎腺炎的非肥胖糖尿病(NOD)小鼠模型中的干燥综合征样疾病治疗有用。
将小鼠分组,一组在饮用水中给予60mg/kg氨溴索,另一组为对照配对喂养动物。通过每周测量刺激唾液量、蛋白质浓度和淀粉酶活性来评估药物治疗的效果。在实验结束时(20周),取出颌下腺和泪腺,通过光学显微镜下的组织学评估来评估淋巴细胞浸润水平。
在12周的治疗过程中,对照小鼠组和接受氨溴索治疗的小鼠组在刺激唾液流量的减少或减少速率方面没有差异。随着动物年龄的增长,蛋白质浓度和淀粉酶损失方面未发现差异。通过SDS-聚丙烯酰胺凝胶图谱和蛋白质免疫印迹分析观察到总蛋白质谱的类似时间变化以及20kDa腮腺分泌蛋白异构体的异常表达。外分泌腺切片的组织学评估未能检测到局灶性淋巴细胞浸润有任何减少。
在自身免疫性涎腺炎的NOD小鼠模型中,氨溴索治疗并未改变干燥综合征样疾病的发展或严重程度。