Eicosanoids and histamine mediate C5a-induced electrolyte secretion in guinea pig ileal mucosa.

C5a is a biologically active polypeptide formed during the course of complement activation and is known to possess histamine-releasing and neutrophil chemotactic properties. In the present study, we have demonstrated that C5a can regulate electrolyte transport across guinea pig ileum, and we have investigated its mechanism of action. Segments of ileum stripped of longitudinal muscle were mounted in Ussing chambers (Krebs' buffer, 37 degrees C, 95% O2/5% CO2) for monitoring short-circuit current (Isc). Serosal application of C5a evoked a transient increase in Isc with an EC50 value of 5.0 nM indicating a potent effect. The C5a-induced increase in Isc was abolished by elimination of both Cl- and HCO3- from the Krebs' solution. Pretreatment with the cyclooxygenase inhibitor indomethacin (5 microM), the neurotoxin tetrodotoxin (0.5 microM) and the H1 receptor antagonist pyrilamine (0.5 microM) reduced the effect of C5a, but the muscarinic antagonist atropine (0.5 microM) was without effect. C5a (100 nM) also evoked the release of histamine (measured by radioimmunoassay in the serosal bathing fluid) by 282% of the control value. In conclusion, in the guinea pig ileum C5a stimulates mucosal anion secretion by releasing histamine and cyclooxygenase products of arachidonic acid. The response is also mediated, in part, via non-chloinergic enteric nerves.

Stereospecific actions of misoprostol on rat colonic electrolyte transport.

Misoprostol (Miso) produces a mild, transient diarrhea in some patients, which is believed to be partly due to intraluminal fluid accumulation. To better understand this diarrheagenic action, we compared the effects of Miso, its 4 stereoisomers (11R16R, 11R16S, 11S16S, 11S16R), misoprostol free acid (Miso-FA), and 16,16-dimethyl PGE2 (dmPGE2) on rat colonic electrolyte transport in vitro. Increases in short-circuit current (Isc) were measured (after serosal addition) in segments of mucosa stripped of muscularis and mounted in Ussing chambers. The rank order of apparent potencies, in terms of threshold, were (microM): 11R, 16S (1.2) approximately dmPGE2 (1.0) > Miso-FA (10.0) approximately Miso >> 11R, 16R; 11S, 16R; 11S, 16S (all inactive at 100 microM). The response to dmPGE2 and Miso was attenuated in the presence of the Na+/K+/Cl- co-transport inhibitor bumetanide (100 microM). Pretreatment with atropine (0.1 microM) did not affect the Isc response to Miso, Miso-FA, or dmPGE2. Tetrodotoxin partially attenuated (39 +/- 9% inhibition) the response to Miso-FA, but did not affect Miso or dmPGE2. In conclusion, Miso increases Cl- secretion across rat colonic mucosa through a direct action on epithelial cells. The activity resides in the 11R,16S isomer, thus implying a stereospecific interaction at PGE receptors. The effect of Miso to stimulate epithelial Cl- secretion might contribute to its diarrheagenic action in vivo.

An in vitro system to screen for diarrheagenic chemicals.

We examined an in vitro system to screen for diarrheagenic chemicals using an established intestinal cell line (T84 human colonic carcinoma). The cells were grown on Millicell-PCF (polycarbonate membrane) wells. The cells were seeded at approximately 5 x 10(6) cells/30mm well and incubated for 9-11 days in a 5% CO2 incubator saturated with water at 37 degrees C. The culture medium was a 1:1 mixture of Ham's F12 and Dulbecco's MEM with 5% fetal bovine serum and 25 micrograms/ml gentamicin sulfate. The well containing cells was removed from the incubator and mounted in a modified Ussing chamber for measurement of short-circuit current (ISC). Chemical-induced increases in ISC are usually indicative of electrogenic epithelial Cl- secretion, which is associated with diarrheagenic effects in animals and humans. T84 cells grown on Millicell-PCF membrane responded with an increase in ISC after basolateral addition of the cholinergic (muscarinic) agonist carbachol, prostaglandin E2, 16,16-dimethylprostaglandin E2, and forskolin, while non-diarrheagenic prostaglandin D2 did not affect ISC. Based on our results, this in vitro system has the potential to be adapted as a rapid screen for detecting diarrheagenic chemicals.

Neurokinin A increases short-circuit current across rat colonic mucosa: a role for vasoactive intestinal polypeptide.

1. Neurokinin A (NKA) is a mammalian tachykinin distributed principally in the nervous system, including the myenteric innervation of the gut. 2. NKA may be involved in neurogenic inflammation and as a modulatory factor in the diarrhoea associated with mucosal inflammation of inflammatory bowel disease (ulcerative colitis). 3. We evaluated the effect of NKA on the short-circuit current ISC, assumed to reflect electrogenic chloride secretion, across muscle-stripped rat colonic mucosa mounted in Ussing chambers. 4. Serosal addition of NKA produced a concentration-dependent (0.1-100 nM) increase in ISC with an EC50 (half-maximal effective concentration) value of 7.5 nM. The maximum (mean +/- S.E.M.) increase in ISC (microA/cm2) for NKA was 111 +/- 10. 5. Tetrodotoxin (0.5 microM) and bumetanide (10 microM), but not atropine (1.0 microM), hexamethonium (100 microM) or pyrilamine (10 microM), significantly inhibited NKA-induced increases in ISC. 6. The response to NKA was attenuated by 45 min pre-treatment with antisera raised against vasoactive intestinal polypeptide (VIP). Moreover, prior desensitization to VIP attenuated the effect of NKA. 7. These studies suggest that NKA increases ISC in rat colon, in part, through a non-cholinergic neural mechanism involving VIP.

Characterization of Ile,Ser-bradykinin-induced changes in short-circuit current across rat colon.

The effects of Ile,Ser-bradykinin (TK) on electrolyte secretion across mucosa of rat distal colon were determined and compared to those of bradykinin (BK). A segment of colon stripped of muscularis was mounted in an Ussing chamber for monitoring short-circuit current (Isc). Serosal application of TK and BK produced a concentration-dependent and transient increase in Isc with EC50(nM) values of 2.0 +/- 0.6 and 1.7 +/- 0.7, respectively. At a concentration of 1.0 microM, TK produced a maximal response of 130 +/- 18 compared to 75 +/- 13 microA/cm2 for BK. Increases in Isc induced by BK and TK were significantly (P less than .001) inhibited (90 +/- 4% for BK and 87 +/- 5% for TK) by serosal addition of bumetanide (10 microM). The lipoxygenase/cyclooxygenase inhibitor, eicosa-5,8,11,14-tetraynoic acid (0.1 mM), inhibited (P less than .01) the response to BK by 67 +/- 9% and to TK by 51 +/- 8%. Moreover, the cyclooxygenase inhibitor indomethacin (5.0 microM) significantly (P less than .05) inhibited the Isc response to 1.0 nM BK and 1.0 nM TK. Atropine (1.0 microM) did not block the effects of either kinin. Finally, the BK antagonist D-Arg0[Hyp3,Thi5,8,DPhe7]-bradykinin (2.0 microM) competitively antagonized the effect of BK and TK, shifting the concentration curve competitively to the right by 6-fold and 16-fold respectively. Another BK antagonist, [D-Phe7]-bradykinin (20 microM), also exhibited similar blockade effects. In this model, although some differences exist, BK and TK appear to act by the same mechanism, which may involve arachidonic acid metabolites.