Wright Megan, Kim Amy, Son Young-Jin
Biology Department, Arcadia University.
J Vis Exp. 2011 Sep 8(55):3124. doi: 10.3791/3124.
Hind limb muscles of rodents, such as gastrocnemius and tibialis anterior, are frequently used for in vivo pharmacological studies of the signals essential for the formation and maintenance of mammalian NMJs. However, drug penetration into these muscles after subcutaneous or intramuscular administration is often incomplete or uneven and many NMJs can remain unaffected. Although systemic administration with devices such as mini-pumps can improve the spatiotemporal effects, the invasive nature of this approach can cause confounding inflammatory responses and/or direct muscle damage. Moreover, complete analysis of the NMJs in a hind limb muscle is challenging because it requires time-consuming serial sectioning and extensive immunostaining. The mouse LAL is a thin, flat sheet of muscle located superficially on the dorsum of the neck. It is a fast-twitch muscle that functions to move the pinna. It contains rostral and caudal portions that originate from the midline of the cranium and extend laterally to the cartilaginous portion of each pinna. The muscle is supplied by a branch of the facial nerve that projects caudally as it exits the stylomastoid foramen. We and others have found LAL to be a convenient preparation that offers advantages for the investigation of both short and long-term in vivo effects of drugs on NMJs and muscles. First, its superficial location facilitates multiple local applications of drugs under light anesthesia. Second, its thinness (2-3 layers of muscle fibers) permits visualization and analysis of almost all the NMJs within the muscle. Third, the ease of dissecting it with its nerve intact together with the pattern of its innervation permits supplementary electrophysiological analysis in vitro. Last, and perhaps most importantly, a small applied volume (-50 μl) easily covers the entire muscle surface, provides a uniform and prolonged exposure of all its NMJs to the drug and eliminates the need for a systemic approach.
啮齿动物的后肢肌肉,如腓肠肌和胫骨前肌,常用于对哺乳动物神经肌肉接头(NMJ)形成和维持所必需信号的体内药理学研究。然而,皮下或肌肉内给药后药物渗透到这些肌肉中往往不完全或不均匀,许多神经肌肉接头可能仍未受影响。虽然使用微型泵等装置进行全身给药可以改善时空效应,但这种方法的侵入性可能会引起混淆的炎症反应和/或直接的肌肉损伤。此外,对后肢肌肉中的神经肌肉接头进行完整分析具有挑战性,因为这需要耗时的连续切片和广泛的免疫染色。小鼠耳廓牵张肌(LAL)是一块薄而扁平的肌肉,位于颈部背侧表面。它是一块快肌,功能是移动耳廓。它包含从颅骨中线起源并横向延伸至每个耳廓软骨部分的头侧和尾侧部分。该肌肉由面神经的一个分支供应,该分支在离开茎乳孔时向尾侧投射。我们和其他人发现,耳廓牵张肌是一种方便的标本,为研究药物对神经肌肉接头和肌肉的短期和长期体内效应提供了优势。首先,它的浅表位置便于在轻度麻醉下多次局部给药。其次,它的薄度(2 - 3层肌纤维)允许可视化和分析肌肉内几乎所有的神经肌肉接头。第三,连同其完整神经一起易于解剖的特点以及其神经支配模式允许在体外进行补充电生理分析。最后,也许最重要的是,少量的给药体积(约50微升)很容易覆盖整个肌肉表面,使所有神经肌肉接头均匀且长时间暴露于药物中,并且无需采用全身给药方法。