Satoh M, Sasaki T, Shimura S, Sasaki H, Takishima T
First Department of Internal Medicine, Tohoku University School of Medicine, Sendai, Japan.
Respir Physiol. 1991 Jun;84(3):379-87. doi: 10.1016/0034-5687(91)90131-2.
We examined the effect of human recombinant TNF alpha on the potential difference (PD) and short circuit current (SCC) of canine tracheal epithelium using an Ussing chamber. Luminal or submucosal TNF (2 to 200 U/ml) produced no significant alterations in the basal PD or SCC values. Pretreatment with luminal TNF significantly reduced isoproterenol (ISOP, 10(-6) M)-evoked increases in SCC and PD to 57% and 66% of that with ISOP alone, respectively, with a significant decrease in conductance (G) to 87% of that with ISOP alone in a dose-dependent fashion, from 10 to 200 U/ml. Even after ISOP (10(-6) M)-evoked PD and SCC had reached a plateau, TNF produced significant decreases in PD and SCC up to 79% and 83% of that with ISOP alone, respectively, in a dose-dependent fashion, from 50 to 200 U/ml. Amiloride did not alter the inhibitory action of TNF on ISOP-evoked SCC and PD values. Antiserum against TNF abolished the inhibitory action of TNF on ISOP-evoked response. In contrast, submucosal TNF did not alter PD, SCC or G. These findings indicate that TNF attenuates beta agonist-evoked increases in chloride secretion across airway epithelium.
我们使用尤斯灌流小室研究了重组人肿瘤坏死因子α(TNFα)对犬气管上皮细胞跨膜电位差(PD)和短路电流(SCC)的影响。管腔或黏膜下给予TNF(2至200 U/ml)对基础PD或SCC值无显著影响。管腔给予TNF预处理可使异丙肾上腺素(ISOP,10⁻⁶ M)诱发的SCC和PD增加分别显著降低至单独使用ISOP时的57%和66%,且电导(G)显著降低至单独使用ISOP时的87%,呈剂量依赖性,剂量范围为10至200 U/ml。即使在ISOP(10⁻⁶ M)诱发的PD和SCC达到平台期后,TNF仍可使PD和SCC分别显著降低至单独使用ISOP时的79%和83%,呈剂量依赖性,剂量范围为50至200 U/ml。氨氯地平不改变TNF对ISOP诱发的SCC和PD值的抑制作用。抗TNF抗血清可消除TNF对ISOP诱发反应的抑制作用。相比之下,黏膜下给予TNF不改变PD、SCC或G。这些发现表明,TNF可减弱β激动剂诱发的气道上皮细胞氯分泌增加。