Lapointe B M, Côté C H
Laval University Hospital Research Center, Ste-Foy, Québec, Canada G1V 4G2.
Am J Physiol. 1999 Sep;277(3):R917-21. doi: 10.1152/ajpregu.1999.277.3.R917.
Anesthetic agents can interfere with measurement of skeletal muscle contractility in vivo or in situ. Data obtained in vitro are however believed to be unaffected by such drugs. Our objective was to compare in vitro contractile measurements of fast- and slow-twitch muscles dissected from rats anesthetized with pentobarbital sodium (PS, 50 mg/kg ip) or with a mixture of ketamine and xylazine (KX, 87. 5:12.5 mg/kg ip). The soleus (Sol) and extensor digitorum longus (EDL) muscles were precisely dissected 10 and 20 min after induction of anesthesia and equilibrated for 20 min in vitro before measuring contractile properties. All data obtained from PS rats were comparable with published values obtained under similar conditions. In EDL, maximum tetanic tension (Po) in KX rats was significantly decreased at both times compared with that in PS muscles. In the Sol, only the muscles exposed for 20 min to KX showed a decreased Po. These results clearly emphasize the need for investigators assessing skeletal muscle contractility in vitro to take into account the type of anesthetics used and the time of in vivo exposition to the drug.
麻醉剂可干扰体内或原位骨骼肌收缩力的测量。然而,体外获得的数据被认为不受此类药物影响。我们的目的是比较从用戊巴比妥钠(PS,50mg/kg腹腔注射)或氯胺酮与赛拉嗪混合物(KX,87.5:12.5mg/kg腹腔注射)麻醉的大鼠身上分离出的快肌和慢肌的体外收缩测量结果。在麻醉诱导后10和20分钟精确解剖比目鱼肌(Sol)和趾长伸肌(EDL),并在体外平衡20分钟后测量收缩特性。从PS大鼠获得的所有数据与在类似条件下获得的已发表值相当。在EDL中,与PS肌肉相比,KX大鼠在两个时间点的最大强直张力(Po)均显著降低。在Sol中,只有暴露于KX 20分钟的肌肉显示Po降低。这些结果清楚地强调,体外评估骨骼肌收缩力的研究人员需要考虑所用麻醉剂的类型以及体内接触药物的时间。