Damas J, Lecomte J
C R Seances Soc Biol Fil. 1976;170(2):482-5.
In the Rat, desensitization to noradrenaline induced by perfusion of large doses of noradrenaline (0.5 to 0.75 mug/mn/100 g), is not suppressed by indomethacine (1 to 5 mg/100 g). Synthesis and release of endogenous prostaglandins of the PGE group are not the cause of the desensitization.
在大鼠中,大剂量去甲肾上腺素(0.5至0.75微克/分钟/100克)灌注诱导的对去甲肾上腺素的脱敏作用,不会被消炎痛(1至5毫克/100克)抑制。PGE组内源性前列腺素的合成与释放不是脱敏作用的原因。