Raulo Saara M, Sorsa Timo, Maisi Päivi
Department of Clinical Veterinary Sciences, Faculty of Veterinary Medicine, Helsinki University, Finland.
Am J Vet Res. 2006 Jul;67(7):1252-7. doi: 10.2460/ajvr.67.7.1252.
To evaluate inhibitory effects of synthetic matrix metalloproteinase (MMP) inhibitors in vitro on gelatinolytic and collagenolytic activities in tracheal epithelial lining fluid (TELF) of horses with recurrent airway obstruction (RAO).
10 horses with RAO and 5 healthy control horses.
Substrate-based functional assays, collagen I and gelatin degradation, were used to measure endogenous collagenolytic and gelatinolytic activities in TELF. In vitro inhibition of MMP activity in TELF with 2 chemically modified tetracyclines (CMTs; CMT-3 and CMT-8) and 2 bisphosphonates (BPs; zoledronate and pamidronate) was evaluated.
CMT-3, CMT-8, zoledronate, and pamidronate in a dose-dependent manner inhibited TELF type I collagenolytic and gelatinolytic activities, although no complete inhibition of TELF type I collagenolytic and gelatinolytic activities was achieved with the inhibitor concentrations of 25 to 500 microM tested. The CMTs inhibited pathologically induced collagen I degradation more effectively than BPs. Of the tested CMTs, CMT-3 was the most effective inhibitor of gelatinolytic activity, and the efficiency of CMT-3 corresponded with that of the BPs.
An increase in MMP activity in the equine respiratory tract may potentially be inhibited by administration of CMTs or BPs. Distinct synthetic MMP inhibitors may eventually provide an additional means for pharmacologic treatment by decreasing ongoing active tissue destructive inflammation associated with chronic lung disease. The MMP inhibitors such as CMTs and BPs that are targeted to solely inhibit a pathologic increase in MMP activities provide the advantage of minimal adverse effects that are characteristics of other excessively potent MMP inhibitors.
评估合成基质金属蛋白酶(MMP)抑制剂在体外对复发性气道阻塞(RAO)马匹气管上皮衬液(TELF)中明胶分解和胶原分解活性的抑制作用。
10匹患有RAO的马和5匹健康对照马。
采用基于底物的功能测定法,即I型胶原和明胶降解法,来测量TELF中的内源性胶原分解和明胶分解活性。评估了2种化学修饰四环素(CMT;CMT-3和CMT-8)和2种双膦酸盐(BP;唑来膦酸盐和帕米膦酸盐)对TELF中MMP活性的体外抑制作用。
CMT-3、CMT-8、唑来膦酸盐和帕米膦酸盐均以剂量依赖性方式抑制TELF的I型胶原分解和明胶分解活性,尽管在测试的25至500微摩尔抑制剂浓度下,未完全抑制TELF的I型胶原分解和明胶分解活性。CMT对病理诱导的I型胶原降解的抑制作用比BP更有效。在测试的CMT中,CMT-3是明胶分解活性最有效的抑制剂,其效率与BP相当。
给予CMT或BP可能会抑制马呼吸道中MMP活性的增加。不同的合成MMP抑制剂最终可能通过减少与慢性肺病相关的持续活跃的组织破坏性炎症,为药物治疗提供额外手段。专门针对抑制MMP活性病理性增加的MMP抑制剂,如CMT和BP,具有其他强效MMP抑制剂所具有的不良反应最小的优势。