Schleip R, Klingler W, Wearing S, Naylor I, Zuegel M, Hoppe K
Division of Neurophysiology Ulm University, Albert-Einstein-Allee 23, 89081 Ulm, Germany.
J Musculoskelet Neuronal Interact. 2016 Sep 7;16(3):256-60.
While two laboratory techniques are commonly used to assess the tensile properties of muscle tissue, emerging evidence suggests that the fascial components of these tissues also serve an active role in force generation. Hence, we investigated whether these techniques are sensitive for assessment of fascial micromechanics.
Force measurements on dissected fascial tissue were performed either using the classical immersion organ bath or using an improved superfusion approach simulating pulsed pharmacological triggers. Rat deep dorsal fascial strips as well as rat testicular capsule were pharmacologically challenged either with mepyramine or oxytocin.
The classical immersion technique yielded a lower force response to mepyramine than the superfusion method (median: 367.4 vs. 555.4µN/mm(2)). Pause in irrigation before application reduced irregularities during bolus application. The superfusion approach was improved further by the following points: The high sensitivity of the superfusion method to bolus addition was voided by deviation of fluid supply during bolus addition.
Although both methods demonstrated pharmacologically induced contractile responses in lumbar fascia samples, the modified superfusion method may improve force registrations of slow contracting fascial tissue and minimize artefacts of fluid application.
虽然通常使用两种实验室技术来评估肌肉组织的拉伸特性,但新出现的证据表明,这些组织的筋膜成分在力的产生中也发挥着积极作用。因此,我们研究了这些技术对筋膜微观力学评估是否敏感。
对解剖后的筋膜组织进行力测量,要么使用经典的浸泡器官浴,要么使用模拟脉冲药理学触发的改进的灌注方法。用美吡拉敏或催产素对大鼠深背筋膜条以及大鼠睾丸包膜进行药理学刺激。
经典浸泡技术对美吡拉敏产生的力反应低于灌注方法(中位数:367.4对555.4µN/mm(2))。给药前暂停冲洗可减少推注给药期间的不规则情况。灌注方法通过以下几点得到进一步改进:推注给药期间通过液体供应偏差消除了灌注方法对推注添加的高敏感性。
虽然两种方法在腰部筋膜样本中均显示出药理学诱导的收缩反应,但改良的灌注方法可能会改善缓慢收缩筋膜组织的力记录,并使液体应用的伪像最小化。