The effect of non-steroidal anti-inflammatory drugs on the electrical properties of cultured dog tracheal epithelial cells
The effect of non-steroidal anti-inflammatory drugs (NSAIDs) on the electrical properties of primary cultures of dog tracheal epithelium has been studied. The cells used were grown with an air interface in a serum-free medium on membranes coated with human placental collagen. When mounted in Ussing...
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Veröffentlicht in: | European journal of pharmacology 1994-02, Vol.252 (2), p.183-188 |
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Sprache: | eng |
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Zusammenfassung: | The effect of non-steroidal anti-inflammatory drugs (NSAIDs) on the electrical properties of primary cultures of dog tracheal epithelium has been studied. The cells used were grown with an air interface in a serum-free medium on membranes coated with human placental collagen. When mounted in Ussing chambers at 37°C, mean values for the baseline short circuit current (
I
sc) and the transepithelial resistance of 65 tissue specimens from 18 dogs were
24.0 ± 3.2 μ
A/cm
2
and 458 ± 128 Ω ·
cm
2
, respectively. These tissues had been pretreated with amiloride to abolish active Na
+ absorption. Under these conditions, the
I
sc value serves as a measure of active Cl
− secretion. The results of this study revealed that the
I
sc across a cultured monolayer of trachea was attenuated by the tested NSAIDs, indomethacin, fulfenamic acid, mefenamic acid, aspirin, and acetaminophen, with
K
i's that ranged from 6.0 × 10
−5 to 2.51 × 10
−3 M. Salicylic acid had no effect on baselin
I
sc. Cl
− channel inhibitors tested was: fulfenamic acid ⪢ indomethacin > mefenamic acid ⪢ aspirin > acetaminophen > salicylic acid. The NSAIDs also significantly inhibited both the transient, Ca
2+-dependent and the sustained, cAMP-dependent increases in
I
sc elicited by isoproterenol. Thus, the tested NSAIDs appeared to have an effect on the electrical properties of the cells. A similar effect of NSAIDs on ion transport across the human airway epithelium may help to reduce airway fluid secretion. |
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ISSN: | 0014-2999 1879-0712 |
DOI: | 10.1016/0014-2999(94)90595-9 |