- Open Access
Role of taurine on acid secretion in the rat stomach
© Huang et al; licensee BioMed Central Ltd. 2011
- Received: 22 October 2010
- Accepted: 5 February 2011
- Published: 5 February 2011
Taurine has chemical structure similar to an inhibitory neurotransmitter, γ-aminobutyric acid (GABA). Previous studies on GABA in the stomach suggest GABAergic neuron is involved in acid secretion, but the effects of taurine are poor understood.
The effects of taurine on acid secretion, signal transduction, and localization of taurinergic neurons were determined in the rat stomach using everted whole stomach, RIA kit and immunohistochemical methods.
We used antibodies against taurine-synthesizing enzyme, cysteine sulfuric acid decarboxylase (CSAD), and taurine. CSAD- and taurine-positive cells were found in the muscle and mucosal layers. Distributions of CSAD- and taurine-positive cells in both mucosal and muscle layers were heterogeneous in the stomach. Taurine at 10-9~10-4 M induced acid secretion, and the maximum secretion was at 10-5 M, 1.6-fold higher than the spontaneous secretion. Taurine-induced acid secretion was completely inhibited by bicuculline and atropine but not by cimetidine, proglumide, or strychnine. Atropine and tetrodotoxin (TTX) completely inhibited the acid secretion induced by low concentrations of taurine and partially inhibited induced by high concentrations. Verapamil, a calcium blocker agent, inhibited acid output elicited by taurine. We assumed all Ca2+ channels involved in the response to these secretagogues were equally affected by verapamil. Intracellular cAMP (adenosine 3', 5'-monophosphat) in the stomach significantly increased with taurine treatment in a dose-dependent manner. High correlation (r=0.859, p < 0.001) of taurine concentrations with cAMP was observed.
Our results demonstrated for the first time in taurine-induced acid secretion due to increase intracellular calcium may act through the A type of GABA receptors, which are mainly located on cholinergic neurons though cAMP pathway and partially on nonneuronal cells in the rat stomach.
- Acid Secretion
- GABAA Receptor
- Parietal Cell
- Cholinergic Neuron
Inhibitory amino acids (IAAs), e.g., taurine and γ-aminobutyric acid (GABA), are present in various parts of the vertebrate central nervous system (CNS) and serve as major inhibitory neurotransmitters . Taurine is the most abundant free amino acid in the body and is present at high concentrations during development. It is synthesized from cysteine via oxidation of cysteine to cysteinesulfinate by the enzyme cysteine dioxygenase (CDO), followed by the decarboxylation of cysteinesulfinate to hypotaurine, catalyzed by cysteine sulfuric acid decarboxylase (CSAD) [2, 3].
Taurine has many physiological properties, including membrane stabilization, osmoregulation, neuromodulation, regulation of calcium homeostasis, antioxidation, modulation of ion flux, and serving as a neurotransmitter or neuromodulator [4–8].
Taurine has chemical structure similar to an inhibitory neurotransmitter GABA which binds to GABAA, GABAB, and the glycine receptor [9–12]. It protected the gastric mucosa against certain lesions [13–16]. Taurine is stored in parietal cells  and smooth muscle . It plays an import role in stabilizing membranes , and modulating acid secretion and gastric motility.
Studies on GABA in the enteric nervous system suggested that GABAergic neurons are not confined to the CNS, but rather these neurons also exist in the peripheral autonomic nervous system [19–21] and are involved in acid secretion  and motility . However, the functions of taurine in gastric secretion are largely unknown. Recently, pharmacological studies have found that taurine binds to GABA receptors [24–26]. The purpose of the study was to determine if taurine also regulates gastric acid secretion via GABA receptors in the stomach.
Localization of taurine in the CNS used enzymatic synthesis of CSAD enzymes [10, 11]. CSAD forms antibodies in the hippocampus, cerebellum, and retina [27–29]. However, no detailed information is available for the stomach.
In this communication, we demonstrated that taurine might regulate acid secretion through A- type GABA receptors and elevation of cAMP in the stomach. The distribution of taurine-containing cells in the rat stomach was localized immunohistochemically using specific antibodies against taurine and CSAD.
Chemical and antibodies
Taurine, bicuculline, cimetidine, proglumide, atropine, strychnine, tetrodotoxin (TTX), verapamil, and 3-isobutyl-1-methylxanthane (IBMX) were purchased from Sigma Chemical (St. Louis, MO, USA). The [3H] cAMP (adenosine 3', 5'-monophosphat) assay system was obtained from Amersham (Buckinghamshire, UK). Anti-taurine was purchased from Abcam (Cambridge, UK). Anti-CSAD was a gift from Dr. Wu, J-Y (Department of Biomedical Science, Florida Atlantic University, Boca Raton, Florida 33431, USA). Other chemicals used were of reagent grade and were obtained from various commercial sources.
Male Sprague-Dawley rats (National Laboratory Animal Center, Taipei, Taiwan) weighing 180~250 g were used. They were housed in group cages under controlled illumination (light cycle, 08:00~20:00), relative humidity of 30%~70%, and temperature (23 ± 1°C) with free access to a laboratory diet (LabDiet, Brentwood, MO, USA) and tap water. Approval for the study was obtained from the Animal Care and Use Committee of Taipei Medical University.
The immunohistochemical procedures were described in detail elsewhere . Briefly, male Sprague-Dawley rats were initially anesthetized with an intraperitoneal injection of sodium pentobarbital (50 mg/kg), followed by perfusion with 1 L saline at 37°C, and subsequent fixation with 4% paraformaldehyde in phosphate-buffered saline (PBS: 50 mM potassium phosphate buffer (pH 7.4) containing 0.9% NaCl) at 4°C. After fixation, the tissue was frozen, embedded in OTC compound, mounted on a gelatinized slide, and sectioned at 20~30 μm. The body and antrum of the stomach were used for immunohistochemical studies by the peroxidase-antiperoxidase (PAP) technique . Tissue sections were treated in the following manner: (i) incubated with anti-CSAD (1:300) or anti-taurine (1:1000; Abcam) (diluted in 0.1 M PBS containing 0.1% Triton X-100) for 16 h at 4°C; (ii) rinsed twice with 0.1 M PBS; (iii) incubated in PAP solution (at a 1:50 dilution) in 50 mM Tris-HCl (pH 7.6) for 2 h at room temperature; (iv) rinsed with 50 mM Tris-HCl (pH 7.6) twice; (v) incubated in a solution containing 0.05% diaminobenzidine and 0.01% H2O2 in 50 mM Tris-Cl (pH 7.6), for 8~10 min at room temperature; and (vi) the sections were dehydrated, mounted on slides with Permount (Fisher), and covered with cover slips for light-microscopic examination. For control experiments, sections were treated exactly as those described above for the experimental group except that antibodies had been preabsorbed with an excess of respective antigens and then were used to replace the anti-taurine or anti-CSAD. Anti-CSAD as described elsewhere . Taurine-containing cells were determined by using specific antibodies from Abcam. For the control experiments anti-taurine and anti-CSAD sera were replaced with preimmune rabbit serum at the same dilution.
Experiments on Everted Whole Stomachs
Experiments on everted whole stomachs were performed as described elsewhere , with slight modifications. Briefly, male Sprague-Dawley rats (weighing 180~250 g) were deprived of food overnight, and allowed free access to water to ensure that the stomach was free of solid contents. A rat was decapitated, and its stomach was immediately removed. The entire everted organ was then placed in a 20-ml organ bath containing a mucosal saline solution (in mM: NaCl, 119; KCl, 4.7; CaCl2, 2.5; and glucose, 5.6; pH 5.2) at 30 ± 1°C and continuously bubbled with 100% O2. The serosal side was perfused with a serosal saline solution (in mM: NaCl, 119; KCl, 4.7; CaCl2, 2.5; NaHCO3, 25; KH2PO4, 1.03; and glucose, 5.6; pH 7.4) at a rate of 1 ml/min under the same conditions as described above except that 100% O2 was replaced by a mixture of 95% O2 and 5% CO2. One hour after equilibration of the organ, the mucosal saline solution was replaced every 15 min during the experiment. Only the serosal side of the preparation was exposed to the test drugs.
Spontaneous acid secretion was determined for 60 min before adding the test drugs. Acid secretion was allowed to last for an additional hour. The acid accumulated on the mucosal side was initially titrated to pH 5.2 and pH 7.0 with 0.1 mM NaOH. Responses of the stomach to drug treatments were expressed as the secretory ratio (R), which was defined as:
R = (secretion evoked by the drug)/(average spontaneous secretion).
The average spontaneous secretion was calculated using acid from the four periods immediately before exposure to the test drugs. Finally, the secretory ratio at the peak response was measured to assess the concentration-response curves.
Measurement of the cAMP Concentration
Stomachs were cut into 0.4 × 0.4-mm cubes with a Mellwain tissue chopper. After preincubation in a serosal saline solution containing 0.5 mM IBMX maintained at 37°C and continuously bubbled with 95% O2 and 5% CO2. They were incubated in medium containing 0.5 mM IBMX for 30 min. The mixture was incubated 2 min in the presence or absence of different doses of taurine (10-9~10-4 M) according to protocols provided by the supplier (RPA 538; Amersham Biosciences).
After incubation, tissues were homogenized in 6% trichloroacetic acid, followed by centrifugation at 3,000 g and 4°C for 15 min. The supernatant was neutralized to pH 7.4 with 1 M Tris, followed by extraction with ether four times. The ether extracts were combined and dried. The cAMP concentration was determined using a commercial RIA kit. The homogenized solution was solubilized in 3 N NaOH and used for protein determination as previously described .
Results are expressed as the mean ± SEM (n = sample number). Data were analyzed by Dunnett's test or Student's t-test; a p value of ≤ 0.05 was considered statistically significant.
Measurement of the cAMP Concentration
In this communication we further support the notion that taurine may play an important role in the stomach. First, taurine markedly increases gastric acid secretion. Second, taurine stimulates acid secretion that abolished by TTX, atropine, and bicuculline but not by cimetidine, proglumide, or strychnine. Third, taurine potently increases the level of cAMP. Fourth, the presence of taurine-containing cells in the rat stomach is confirmed, as indicated by CSAD- and taurine-positive cells.
We found the presence of taurine-containing cells and taurine-induced acid secretion in the stomach. In the body of the stomach, taurine-immunoreactive cells were observed along the length of the mucosal gland. It had been reported that taurine protects the gastric mucosa from damage caused by monochloramine . Therefore, taurine stored in the mucosal glands may protect cells from self-destruction during oxidation. Taurine-containing cells are present in the myenteric plexus and submucosal plexus of the enteric nervous system in the stomach. Taurinergic neurons in the muscle layer of the gastrointestinal (GI) tract might be involved in motility of the GI tract and the function of endocrine cells as well.
Taurine at 10-6 M markedly stimulated acid secretion in the stomach. Spontaneous acid secretion from the preparation was 1.232 ± 0.067 μmole/15 min, a value similar to the basal acid secretion in vivo  and in vitro . In such preparations, taurine induced acid secretion in a concentration-dependent manner. Therefore, taurine acts not only on the CNS [10, 35–37] but also on the stomach itself to induce acid secretion.
The parietal cells apparently possesses specific receptors for histamine, gastrin, and acetylcholine (ACh) . We found that cimetidine and proglumide had no significant effect on the taurine-induced acid secretion. This suggests that histamine and gastrin may not participate in these events.
TTX completely inhibited the acid secretion induced by low taurine concentration ≤10-7 M but did not completely inhibit the acid secretion induced by high taurine concentration >10-7 M. It's been long recognized that low TTX concentrations blocks nerve conduction due to inhibition of the Na+ channel . The inhibitory effect can be attributed blocking nerve conduction. Atropine completely inhibited acid secretion induced by low taurine concentrations ≤ 10-7 M. Therefore, the neuronal pathway involved in acid secretion induced by low taurine concentrations may predominantly involve in cholinergic neurons. Both TTX and atropine completely inhibited the acid secretion induced by low concentrations of taurine (10-7 M and under). In contrast, there two components in the acid secretion induced by high concentrations of taurine (10-6 M or above). The component insensitive to atropine was to much the same degree as that insensitive to TTX. Whether taurine at high concentrations induces acid secretion by direct action on parietal cells or by indirect actions on other cells remains to be determined.
Taurine is a general agonist for all types of receptors, e.g., GABAA receptors and glycine receptors [10, 40]. Taurine has multiple functions in the brain by participating in both modulation and neurotransmission. Taurine-induced acid secretion was inhibited by bicuculline, an antagonist of the GABAA receptor. Strychnine (10-6 M), a glycine receptor, did not inhibit taurine-induced acid secretion in the stomach. Recently, pharmacological studies have found that taurine binds to GABA receptors [24–26]. There is compelling evidence that taurine interacts with the GABAergic system via the GABAA receptor [24, 41–43]. Taurine as also been shown to activate a taurine receptor  or through the glycine receptor , but the molecular identity of this receptor has not been fully characterized. Yet, studies also indicate that taurine-produced effects can not be simple function. It is interesting that taurine has also been shown can bind to GABA receptors in the rabbit  and the mouse brain  but not pig brain . Thus, different animal species and studies models may produce different results. In the present investigation, taurine can increase acid secretion via the A type of GABAA but not GABAB and glycine receptors in the rat stomach.
Gastric acid secretion is not only stimulated via the classical known neuronal and hormonal pathways but also by the Ca2+-Sensing Receptor (CaSR) located at the basolateral membrane of the acid-secretory gastric parietal cell. More recent studies have shown that in addition to these well described receptors a CaSR has been identified and is active in acid-secretory parietal cells [48–50]. Previous investigation found that verapamil, an inhibitor of L-type Ca2+-channels reduced stimulation suggesting that both the release of intracellular Ca2+ from the ER as well as Ca2+ influx into the cell are involved in CaSR-mediated H+/K+-ATPase activation . Thus, verapamil to block Ca2+-influx from the extracellular space could cause the inhibition of taurine-induced acid secretion.
In addition, taurine effectively increases cAMP concentration in stomach by binding to GABAA receptors on cholinergic neurons, resulting in the excitation of cholinergic neurons, followed by the release of ACh. The ACh-binding M3 receptors exist on the membranes of parietal cells. Extracellular Ca2+ appears to be an important factor in the control of gastric secretion .
Our results demonstrated for the first time in taurine-induced acid secretion due to increase intracellular calcium may act through the A type of GABA receptors, which are mainly located on cholinergic neurons though cAMP pathway and partially on nonneuronal cells in the stomach. In light of the findings of previous investigations together with our observations of CSAD- and taurine-positive cells in the stomach and taurine released from CSAD- and taurine-containing neurons, which is also consistent with the above hypothesis.
If peripheral taurine is involved in modulating gastric function is on way of investigation.
The authors would like to thank Prof. Jang-Yen Wu for kind provision with the Anti-CSAD. This study was financially supported by the Taipei City Hospital (95003-62-153).
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