Table 1

Effect of vasoactive intestinal polypeptide (VIP) antagonism on net Na+ and Cl flux in normal controls, in cholera toxin (CT), Escherichia coli heat labile toxin (LT), and Escherichia heat stable toxin (STa) induced secretion, and on VIP induced decrease in absorption

n Net Cl flux (μmol/min/g) Net Na+ flux (μmol/min/g)
Control112.8 (2.4 to 3.3)6.7 (5.7 to 11.1)
 +VIPa0.273.5 (2 to 4.3)7 (4.5 to 12)
 +VIPa263 (2.5 to 4)6.2 (5 to 13)
CT7−13.1 (−14.6 to−9.9)−7.9 (−10.9 to −6.5)
 +VIPa0.27−3.3 (−8.3 to 1.5)1-a −1.55 (−6.23 to 2.24)1-a
 +VIPa27−1.2 (−4 to 2)1-a −0.5 (−5 to 3.5)1-a
LT6−15.7 (−18 to −12.5)−8.5 (−12.2 to −7.2)
 +VIPa0.27−7 (−11.2 to −5.7)1-a −2 (−6.5 to −1.5)1-a
 +VIPa26−1 (−2.5 to 2)1-a 2 (1.3 to 5)1-a
STa5−10 (−15 to −5.5)−7 (−9.2 to −4)
 +VIPa0.25−3 (−4.5 to 0.5)1-a −2 (−3.2 to 2)1-a
 +VIPa25−2.2 (−3 to 0.2)1-a −1.5 (−3.5 to 2)1-a
VIP0.0251.2 (0.5 to 2.1)3.4 (2.2 to 5.1)
 +VIPa0.252.6 (2.2 to 4)1-b 6 (5 to 10.2)1-b
 +VIPa252.9 (2.2 to 3.8)1-b 7.1 (6.5 to 9.8)1-b
VIP0.25−1 (−1.9 to 1.1)1 (0 to 2.1)
 +VIPa0.251.9 (1.3 to 2.2)c 3.1 (2.5 to 4.5)c
 +VIPa253.2 (2.5 to 4.1)1-b 6.3 (5.2 to 10)1-b
  • Data are median (interquartile range).

  • VIPa0.2, VIPa2, VIP antagonist [4Cl-D-Phe6,Leu17 ]VIP at a dose of 0.2 (VIPa0.2) or 2 μg/kg/min (VIPa2).

  • 1-a p<0.01,

  • 1-b p<0.05, and cp<0.05 compared with the corresponding toxin or VIP alone;ap<0.05,bp>0.05, and cp<0.05 compared with normal controls.