Bonnet P, Argibay J A, White E, Garnier D
Laboratoire d'électrophysiologie et de pharmacologie cellulaires, Parc de Grandmont, Tours, France.
J Comp Physiol B. 1991;161(5):543-7. doi: 10.1007/BF00257911.
In small (less than 300 microns diameter) pulmonary arterial (PA) rings isolated from the cat, hypoxia induced a transient contraction (250 +/- 120 mg, n = 7), whereas in rings of rabbit PA of the same size, hypoxia had no significant effect (n = 19). Precontraction by 40 mmol KCl.1(-1), noradrenaline (NA) 10(-6) mol.1(-1), or histamine (His 10(-5) mol.1(-1)) did not modify this difference between the two species and did not potentiate the hypoxic contraction of small rings of the cat PA. Large rabbit pulmonary arterial segments (300-2000 microns) exhibited no response to hypoxia before precontraction (n = 15). In the presence of procaine (2%) rabbit PA rings (n = 6, small) exhibited no hypoxic contraction. These results in vitro reflect previous in vivo observations.
从猫身上分离出的小直径(小于300微米)肺动脉(PA)环,缺氧可诱导短暂收缩(250±120毫克,n = 7),而在相同大小的兔肺动脉环中,缺氧无显著影响(n = 19)。用40毫摩尔氯化钾.1(-1)、去甲肾上腺素(NA)10(-6)摩尔.1(-1)或组胺(His 10(-5)摩尔.1(-1))预收缩并未改变这两个物种之间的这种差异,也未增强猫肺动脉小环的缺氧收缩。大的兔肺动脉段(300 - 2000微米)在预收缩前对缺氧无反应(n = 15)。在存在普鲁卡因(2%)的情况下,兔肺动脉环(n = 6,小环)无缺氧收缩。这些体外实验结果反映了先前的体内观察结果。