Scheurer U, Drack E, Halter F
J Pharmacol Exp Ther. 1985 Sep;234(3):742-6.
Endogenous prostaglandins have been shown to modify the contractile activity of the intestinal muscle. In this study, the effects of the cyclooxygenase inhibitors phenylbutazone, diclofenac, indomethacin, acetylsalicyclic acid (ASA) and salicyclic acid (SA) on the motility of the Met-enkephalin- (FK) and acetylcholine- (ACh) stimulated isolated rat colon were observed. Intraluminal pressure changes were measured by perfusion manometry in organ preparations maintained in a standard organ bath. FK and ACh dose-dependently increased intraluminal tonic pressure with a response of 42 +/- 0.6 arbitrary units (mean +/- S.E., n = 6) at 10(-6) M FK and of 96.8 +/- 8.6 arbitrary units at 10(-4) M ACh. Oral pretreatment with ASA (300 mg/kg b.i.d. for 3 days and 1 h before removal of the colon) suppressed the stimulatory effect of FK and significantly reduced ACh stimulation of colonic tone. A similar effect was observed when ASA alone was added to the nutrient. Phenylbutazone, diclofenac or indomethacin (10(-4)-10(-3) M) in the nutrient also significantly inhibited the effects of both stimulants. In contrast, p.o. pretreatment with SA (100 mg/kg b.i.d. for 3 days and 1 h before removal of the colon) did not affect stimulatory properties of FK and ACh. SA given with the nutrient exerted a substantial inhibition of the stimulated tone. One-hour washout was sufficient to completely abolish the inhibitory action of SA but reduced that of ASA by only 25%. The data suggest that endogenous prostaglandins and/or thromboxanes are involved in the FK- and ACh-stimulated contraction of rat colonic smooth muscles.(ABSTRACT TRUNCATED AT 250 WORDS)
内源性前列腺素已被证明可改变肠肌的收缩活性。在本研究中,观察了环氧化酶抑制剂保泰松、双氯芬酸、吲哚美辛、乙酰水杨酸(ASA)和水杨酸(SA)对甲硫氨酸脑啡肽(FK)和乙酰胆碱(ACh)刺激的离体大鼠结肠运动的影响。通过在标准器官浴中维持的器官制剂中进行灌注测压来测量腔内压力变化。FK和ACh剂量依赖性地增加腔内张力,在10⁻⁶ M FK时反应为42±0.6任意单位(平均值±标准误,n = 6),在10⁻⁴ M ACh时为96.8±8.6任意单位。口服ASA预处理(300 mg/kg,每日两次,共3天,并在切除结肠前1小时)抑制了FK的刺激作用,并显著降低了ACh对结肠张力的刺激。当单独将ASA添加到营养液中时也观察到类似效果。营养液中的保泰松、双氯芬酸或吲哚美辛(10⁻⁴ - 10⁻³ M)也显著抑制了两种刺激物的作用。相比之下,口服SA预处理(100 mg/kg,每日两次,共3天,并在切除结肠前1小时)不影响FK和ACh的刺激特性。与营养液一起给予的SA对刺激的张力有显著抑制作用。1小时的洗脱足以完全消除SA的抑制作用,但仅将ASA的抑制作用降低25%。数据表明内源性前列腺素和/或血栓素参与了FK和ACh刺激的大鼠结肠平滑肌收缩。(摘要截短至250字)