Stephens N L, Kroeger E A, Kromer U
Am J Physiol. 1975 Feb;228(2):628-32. doi: 10.1152/ajplegacy.1975.228.2.628.
In multi-unit tracheal smooth muscle (TSM), quick stretches applied at a velocity of 5 times the measured maximum velocity of isotonic shortening of the muscle, of a magnitude 3 times the measured extension of the series-elastic component when the muscle contracts maximally, and at optimal muscle length (L-o) were unable to elicit any myogenic response (MR). Experimental conditions such as hypoxia (P-O2 smaller than 60 mmHg) and acidosis (pH equals 6.8) or the presence of Ba2+ (2 mM), acetylcholine (10-6 M), or high (K+)-o (59 mM) were also unable to elicit the MR. However, tetraethylammonium chloride (TEA, 0.4-67 mM) produces 1) spontaneous phasic contractions and 2) a MR to quick stretch. The ionic basis for these changes was then investigated by studying the Ca and Mg dependence of the response to TEA. The dose-response relationship to TEA was shifted to the left by decreasing external Mg2+ from 2.5 to 0.5 mM. The ability of TSM to produce a MR was absolutely dependent on external Ca, but the threshold concentration required shifted from 2.5 times 10-5 M at normal external Mg (2.5 mM) to 5 times 10-4 M at the reduced external Mg (0.5 mM). The effects of TEA on spontaneity and the MR were abolished by D-600. These results suggest that 1) TEA functionally converts multiunit smooth muscle into a single unit one and leads to the development of a MR and 2) the MR results from a depolarization-activated mobilization of Ca and is inhibited by ionic conditions known to increase membrane permeability.
在多单位气管平滑肌(TSM)中,以肌肉等张收缩测量的最大速度的5倍的速度进行快速拉伸,拉伸幅度为肌肉最大收缩时串联弹性成分测量伸长的3倍,且在最佳肌肉长度(L-o)下进行拉伸,未能引发任何肌源性反应(MR)。诸如缺氧(P-O2小于60 mmHg)和酸中毒(pH等于6.8),或存在Ba2+(2 mM)、乙酰胆碱(10-6 M)或高(K+)-o(59 mM)等实验条件也未能引发MR。然而,四乙铵氯化物(TEA,0.4 - 67 mM)会产生1)自发性相位收缩和2)对快速拉伸的MR。然后通过研究对TEA反应的钙和镁依赖性来探究这些变化的离子基础。将外部Mg2+从2.5 mM降至0.5 mM会使对TEA的剂量反应关系向左移动。TSM产生MR的能力绝对依赖于外部钙,但所需的阈值浓度从正常外部镁(2.5 mM)时的2.5×10-5 M转变为降低外部镁(0.5 mM)时的5×10-4 M。D-600消除了TEA对自发性和MR的影响。这些结果表明:1)TEA在功能上将多单位平滑肌转变为单单位平滑肌并导致MR的产生;2)MR源于去极化激活的钙动员,并受到已知会增加膜通透性的离子条件的抑制。