Greenberg S S, Wang Y, Xie J, Smartz L, Rammazatto L, Curro F A
LSU Medical Center, Department of Medicine, New Orleans 70112.
J Dent Res. 1991 Sep;70(9):1278-85. doi: 10.1177/00220345910700090901.
Thromboxane A2 (TXA2), a potent vasoconstrictor agent, is released from platelets and smooth muscle during inflammation and trauma. TXA2 may cause lingual artery (LA) contraction, leading to lingual paresthesia. The effects of U-46619, a TxA2 mimetic, on isolated rings of canine LA and mesenteric artery (MA) were examined. U-46619 (1 nmol/L to 1 mumol/L) caused a triphasic contraction of LA and MA; a rapid, phasic contraction; a slow, sustained contraction; and, upon washout of U-46619, a maintained contraction. The MA relaxed slowly, but the LA remained contracted for at least three h after washout. Decreasing extracellular calcium ion (Ca2+o) to less than 0.1 mumol/L with 2 mmol/L EGTA relaxed MA, but not LA. EGTA (4 mmol/L) partially relaxed the maintained contraction of LA. Inhibition of protein kinase C with amphotericin B or staurosporine inhibited the phasic and sustained contractions of LA, but did not affect the maintained contraction in the presence or absence of EGTA. Thus, CA2+o was required for the initial contraction of the LA by U-46619, but did not appear to be required for the maintained contraction following washout of U-46619. The data support the conclusion that following a brief exposure to U-46619, maintained contraction of LA persists by a unique mechanism that may be independent of Ca2+ and protein kinase C. Sustained LA contraction after exposure to endogenous TXA2 during inflammation and trauma may contribute to impaired lingual blood flow and orofacial tissue injury.
血栓素A2(TXA2)是一种强效血管收缩剂,在炎症和创伤期间从血小板和平滑肌中释放出来。TXA2可能导致舌动脉(LA)收缩,进而引起舌感觉异常。研究了TXA2模拟物U-46619对犬LA和肠系膜动脉(MA)离体血管环的影响。U-46619(1 nmol/L至1 μmol/L)引起LA和MA的三相收缩;快速的相性收缩、缓慢的持续性收缩,并且在洗脱U-46619后出现持续性收缩。MA缓慢舒张,但在洗脱后LA至少持续收缩3小时。用2 mmol/L乙二醇双(2-氨基乙醚)四乙酸(EGTA)将细胞外钙离子(Ca2+o)浓度降低至小于0.1 μmol/L可使MA舒张,但不能使LA舒张。EGTA(4 mmol/L)可部分缓解LA的持续性收缩。用两性霉素B或星形孢菌素抑制蛋白激酶C可抑制LA的相性和持续性收缩,但在有或无EGTA的情况下均不影响持续性收缩。因此,Ca2+o是U-46619引起LA初始收缩所必需的,但在洗脱U-46619后的持续性收缩中似乎并非必需。这些数据支持以下结论:在短暂暴露于U-46619后,LA的持续性收缩通过一种可能独立于Ca2+和蛋白激酶C的独特机制持续存在。在炎症和创伤期间暴露于内源性TXA2后LA的持续性收缩可能导致舌血流量受损和口腔面部组织损伤。