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Evidence-Based Complementary and Alternative Medicine
Volume 2012 (2012), Article ID 438460, 11 pages
NMDA Receptor-Dependent Synaptic Activity in Dorsal Motor Nucleus of Vagus Mediates the Enhancement of Gastric Motility by Stimulating ST36
1Institute of Acupuncture and Moxibustion, China Academy of Chinese Medical Sciences, 16 Nanxiaojie Street, Dongzhimennei, Beijing 100700, China
2Qingdao Haici Medical Group, 4 Renmin Road, Qingdao 266033, China
3Guanganmen Hospital, China Academy of Chinese Medical Sciences, Beijing 100053, China
4The Affiliated Hospital, Shandong University of Traditional Chinese Medicine, Jinan 250014, China
5Department of Pharmacology, Southern Medical University, Guangzhou 510515, China
6Department of Biomedical Sciences, Florida State University College of Medicine, Tallahassee, FL 32306, USA
Received 12 July 2012; Revised 4 September 2012; Accepted 8 September 2012
Academic Editor: Ying Xia
Copyright © 2012 Xinyan Gao et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Previous studies have demonstrated the efficacy of electroacupuncture at ST36 for patients with gastrointestinal motility disorders. While several lines of evidence suggest that the effect may involve vagal reflex, the precise molecular mechanism underlying this process still remains unclear. Here we report that the intragastric pressure increase induced by low frequency electric stimulation at ST36 was blocked by AP-5, an antagonist of N-methyl-D-aspartate receptors (NMDARs). Indeed, stimulating ST36 enhanced NMDAR-mediated, but not 2-amino-3-(5-methyl-3-oxo-1,2-oxazol-4-yl)propanoic-acid-(AMPA-) receptor-(AMPAR-) mediated synaptic transmission in gastric-projecting neurons of the dorsal motor nucleus of the vagus (DMV). We also identified that suppression of presynaptic μ-opioid receptors may contribute to upregulation of NMDAR-mediated synaptic transmission induced by electroacupuncture at ST36. Furthermore, we determined that the glutamate-receptor-2a-(NR2A-) containing NMDARs are essential for NMDAR-mediated enhancement of gastric motility caused by stimulating ST36. Taken together, our results reveal an important role of NMDA receptors in mediating enhancement of gastric motility induced by stimulating ST36.
Gastric motility disorders are clinically characterized by impaired accommodation, gastroparesis, and dumping syndrome. A large number of studies has been conducted to explore the efficacy of somatic stimulation for the treatment of gastrointestinal motility disorders [1–5]. Reproducible results were generated in both clinical and research settings [6, 7], and several lines of evidence suggest that the gastric motility regulation induced by stimulating ST36 seems to be mediated via vagal reflex in the supraspinal pathway [5, 8–10]. However, how stimulating ST36 regulates gastric motility through relay nuclei and the molecular mechanism employed in this process still remain unclear. Addressing this question can provide valuable clues for the development of effective therapeutics against gastrointestinal motility disorders.
Vagal motor innervation to the major portion of the gastrointestinal (GI) tract is provided by neurons in the dorsal motor nucleus of the vagus (DMV) [11, 12]. Nucleus of the solitary tract (NTS) neurons can potentially contribute input to the DMV and induce potent effects on vagus-mediated gastric function through excitatory glutamatergic and inhibitory GABAergic synaptic connections [13, 14]. Neuropharmacological studies have demonstrated changes in gastric function in response to localized application of gamma-aminobutyric acid (GABA) and glutamate (via GABAa and NMDA receptors) within the DMV [15–18].
In this study, we directly examined the functional role of NMDAR-mediated synaptic transmission in mediating the upregulation of gastric motility by stimulating ST36. Our data reveal that electroacupuncture at ST36 upregulates gastric motility by specifically enhancing the glutamate-receptor-2a-(NR2A-) containing N-Methyl-D-aspartate-receptors-(NMDAR-) mediated synaptic transmission in gastric-projecting DMV neurons.
2. Materials and Methods
2.1. Animals and Surgical Preparation for In Vivo Experiments
Adult male Sprague Dawley (250–300 g) rats were purchased from the Institute of Laboratory Animalsciences, CAMS and PUMC (Beijing, China). In this study, all manipulations and procedures were carried out in accordance with The Guide for Care and Use of Laboratory Animals issued by USA National Institutes of Health and were approved by the Institutional Animal Care and Use Committee of China Academy of Chinese Medical Sciences. As described previously [19, 20], rats were housed (°C) in groups and maintained under a 12 hours light/dark cycle with food and water available ad libitum. The rats were fasted overnight with free access to water in proxima luce, and anesthetized with an intraperitoneal injection of urethane (1.0 g/kg, Sigma-Aldrich, St. Louis, USA). The left common carotid artery was cannulated with a polyethylene catheter filled with physiological saline containing heparin (200 IU/mL, LEO, Denmark) for recording of arterial pressure (AP) via a blood pressure transducer (TSD104A) and amplifier (MP150, DA100C, BIOPEC, Goleta, USA). The trachea was cannulated but not immobilized, to avoid respiratory tract congestion and a catheter was inserted into the left jugular vein for solution. A 2-mm-diameter polyurethane tube attached to a 1-cm-diameter latex balloon was inserted into the stomach through the mouth and esophagus. A syringe was attached to the cannula to inflate and deflate the balloon with water. The balloon was filled with 0.5–1.5 mL warm-water (37°C), which is equal to 80–150 mm H2O pressure, and the pressure was measured by a transducer connected to an amplifier through a thin polyethylene tube (1.5-mm in o.d.) and recorded by a multichannel data acquisition workstation (Micro1401-3, Cambridge Electronic Design, England). Offline data analysis was conducted with spike2 software. Semifasting gastric motor activity was recorded as a control for at least 1 hour before somatic stimulation. C57BL/6J or NR2A knockout mice (6–8 weeks) were purchased from Riken Bioresource Center, Japan and were treated with the protocol similar to the above.
2.2. Microinjection in DMV
A glass micropipette (i.d.: 0.04 mm; o.d.: 0.12 mm; WPI, Sarasota, USA) with a tip diameter of ~30 μm was stereotaxically placed at 0.1 to 0.6 mm rostral to calamus scriptorius (CS), 0.3 to 0.6 mm lateral from the midline, and 0.5 to 0.9 mm below the dorsal surface of the medulla. Microinjections of glutamate or GABA receptor (GABAR) antagonist were performed bilaterally via a Hamilton syringe (Mode 75) connected to the micropipette, with the movement of the meniscus monitored by a dissecting microscope. Injections were given in volumes of 20 nL over a period of 10–15 seconds. Somatic-stimulation-evoked responses were repeated 5 minutes after the DMV microinjection. The locations of microinjection were confirmed by histological verification.
2.3. Histological Verification of Injection Sites
The microinjection site in the brainstem was marked by pontamine sky blue. After fixing in vivo with 2% paraformaldehyde and 1% glutaraldehyde in 0.1 M PBS (pH 7.4), the brainstem was sectioned at 30 μm, and the sections were stained with 0.3% neutral red. The marked microinjection site was located by microscopic examination. Only those data with histological and chemical confirmation were accepted.
The stimulation electrode was placed at ST36, a hind limb point at which electroacupuncture or manual acupuncture enhances gastric motility . Based on the descriptions in previous reports , the location is on the anterolateral side of the hind limb near the anterior crest of the tibia below the knee under the tibialis anterior muscle. This point was bilaterally stimulated with a 2-3 mA pulse of 0.5 ms duration at a frequency of 4 Hz for 30 seconds or 20 min by a pair of needle-electrodes inserted 3 mm depth into the skin. As a control, we selected CV12 which is located on the median line of the upper abdomen, 1.5 cm above the umbilicus, and could inhibit gastric motility . The abdomen point was also inserted to a depth of 3 mm and stimulated with the same protocol. The electrical current for somatic stimulation was generated by a stimulator (SEN-7203, NIHON KOHDEN, Tokyo, Japan). For the recording of intragastric pressure in vivo, electroacupuncture was given at least 1 hour after stable basal recording or 10 min after drug administration. In brain slice experiments, we stimulated ST36 for 20 minutes in rats with retrograde labeling after anesthetization and then cut brain slices.
2.5. Retrograde Labeling
Retrograde neuronal tracer 1,1′-dioctadecyl-3,3,3′,3′-tetramethylindocarbocyanine perchlorate (DiIC18(3); DiI) (Molecular Probes) was used to label gastric-projecting neurons of the DMV in 14-day-old male Sprague Dawley rats (Institute of Laboratory Animal Sciences, CAMS and PUMC, Beijing, China). As described previously [11, 22], after anesthetizing deeply with urethane and performing an abdominal laparotomy, DiI crystals were applied to one gastric region per rat (either the major curvature of the fundus or corpus or the antrum-pylorus). To confine the site of application, the crystals were embedded to the application site using a fast-settling epoxy resin that was allowed to harden for several minutes. After closing the laparotomy with 5/0 suture, the animals were placed in the chamber warmed under a radiant heat lamp until normal activity was restored. The animals were then returned to their home cages and allowed to recover for 10–15 days before brain slices were collected.
2.6. Brain Slice Preparation
Thin brainstem slices were prepared from retrograde-labeled rats as described previously with several modifications [11, 22]. Briefly, the rat was sacrificed after being deeply anesthetized with urethane. The whole brain was then removed and placed in ice-cold artificial cerebrospinal fluid (ACSF) containing (mM): 124 NaCl, 3 KCl, 1.25 NaH2PO4, 1.3 MgSO4, 2 CaCl2, 26 NaHCO3, 10 glucose, bubbled with 95% O2/5% CO2, osmolality 300–310 mOsm. After removing the cerebellum, the brainstem was transected rostrally at the level of the pons and again at a point several millimeters caudal to the CS. A vibratome (VT1200S, Leica, German) was used to cut four to five coronal slices (250 μm thickness) containing the DMV. The slices were incubated at 37°C for at least 45 minutes in oxygenated ACSF before use.
2.7. Whole Cell Recording
A single slice was transferred to the recording chamber and kept in place with a slice anchor (Warner Instruments, Hamden, USA). The retrograde-labeled DMV neurons were identified under a Nikon E600 microscope (Nikon, Tokyo, Japan) equipped with tetramethylrhodamine isothiocyanate epifluorescence filters. Electrophysiological recordings were made under brightfield illumination after the identity of a labeled neuron was confirmed. The slice was continuously superfused with oxygenated ACSF (2 mL/min) at room temperature. Recording solution containing (in mM): 145 K-gluconate, 7.5 KCl, 9 NaCl, 1 MgSO4, 10 HEPES, 0.2 EGTA, 2 Na-ATP, 0.25 Na-GTP, adjusted to pH 7.4 with KOH, osmolality 290–300 mOsm, was used to back-fill recording electrodes (DC resistance: 5–7 MΩ). Currents were recorded with a MultiClamp700B amplifier (Molecular Devices) and filtered at 2 kHz with a lowpass filter, and data were digitized at 10 kHz and stored online using the pClamp10 software.
For recording of mini-EPSC (mEPSC), the perfusion solution contained 30 μM bicuculline and 1 μM TTX, and the membrane was held at −60 mV. Data were analyzed with the Mini Analysis program (Synaptosoft, Leonia, USA).
For electrical stimulation-induced EPSCs, a concentric tungsten bipolar stimulating electrode (WPI, Sarasota, USA) was placed in the centralis or medialis subnuclei of the NTS. Single stimulus pulse (200 μs, 10–500 μA) or pairs of stimuli (200 μs, 10–500 μA, 100 ms interval) were applied every 20 seconds to evoke EPSCs. The above stimulation intensity is a range which can induce 50% of maximum AMPAR- or NMDAR-mediated EPSC. Series resistance ranged from 12 to 16 MΩ, and input resistance is 260–290 MΩ. The series and input resistances were monitored using voltage steps (5 mV, 50 ms) at 20-second intervals throughout the whole recording. If the membrane resistance changes more than 20% relative to an initial 3-minute period of recordings, the neuron will be rejected from the statistical analysis. Non-NMDAR- (AMPA/kainite-) and NMDAR-mediated EPSCs were recorded at a holding potential of −60 mV and +40 mV. 30 μM bicuculline or 20 μM 6,7-dinitroquinoxaline-2,3-dione (DNQX) was bath-applied to block GABAR or AMPA receptor (AMPAR) current. 5 mM QX314 was added to recording solution to prevent antidromically activated action potentials. Neurons were allowed to recover fully between additions of antagonists (minimum washout period of 10 minutes). Antagonists were superfused for at least 5 minutes. All chemicals or drugs are purchased from Sigma-Aldrich (St Louis, USA) if not stated otherwise.
2.8. Data Analysis
Data are shown as mean ± SEM. For significance evaluation, data sets with normal distribution were analyzed by paired or unpaired test for two groups or one-way ANOVA followed by test or Dunnett’s test for more than two groups, and was considered statistical significance.
3.1. Electroacupuncture at ST36 Increases Gastric Motility through Activating DMV Neurons
To determine whether electroacupuncture at ST36 may affect gastric motility in rats, we designed an experiment in which an electrical stimulation with 2-3 mA pulse of 0.2 ms duration at a frequency of 4 Hz was applied to ST36 or CV12. As shown in Figure 1(a), gastric pressure was dramatically increased by the low frequency stimulation at ST36. On the contrary, stimulating CV12 caused a marked reduction in gastric pressure. On average, gastric pressure was increased mm H2O (, ) by stimulation at ST36, but decreased mm H2O (, ) by stimulating CV12. Thus, these data suggested that low frequency stimulation at ST36 can regulate gastric motility in a location-specific manner.
To identify the role of glutamate or GABA receptors of DMV neurons in mediating the enhancement of gastric motility by electroacupuncture at ST36, we stereotaxically microinjected antagonists for either GABAa receptor bicuculline (2 nL, 30 μM), or glutamate receptor including DNQX (2 nL, 20 μM) for AMPARs and AP5 (2 nL, 50 μM) for NMDARs into DMV. The increased gastric pressure induced by stimulating ST36 was significantly reduced by AP5 ( mm H2O, , ), but not by bicuculline ( mm H2O, , ) or DNQX ( mm H2O, , ) (Figures 1(a) and 1(b)), suggesting that low frequency stimulation at ST36 increases gastric motility through activating NMDARs, rather than AMPARs or GABARs in DMV neurons.
3.2. Electroacupuncture at ST36 Enhances NMDAR-Mediated EPSCs in Gastric-Projecting DMV Neurons
To address whether electroacupuncture at ST36 specifically affects the NMDAR-mediated synaptic responses in gastric-projecting DMV neurons, we first used a retrograde tracing marker to label gastric-projecting DMV neurons. Similar to previous reports [11, 23, 24], a majority of labeled neurons were localized at the medial DMV and had small somas and few branches (Figure 2(a)). We then stimulated ST36 for 20 minutes in rats with retrograde labeling, and carried out whole cell recording in acute brainstem slices. In labeled DMV neurons, NMDAR-mediated EPSC in ST36 group was significantly larger than that in the control group without stimulation ( pA versus pA, , ) (Figures 2(b) and 2(c)). By contrast, no significant difference was found in AMPAR-mediated EPSCs between ST36 and control groups in labeled DMV neurons ( pA versus pA, , ) (Figures 2(b) and 2(d)). On the other hand, neither NMDAR nor AMPAR mediated EPSC in unlabeled DMV neurons had significant changes in either ST36 or control group (NMDAR-mediated EPSC: pA for stimulated versus pA for control, , ; AMPAR-mediated EPSC: pA for stimulation versus pA for control, , ) (Figures 2(b)–2(d)). As shown in Figure 2(e), AMPA/NMDA current ratio of labeled neurons in ST36 group decreased significantly compared to the unlabeled neurons ( for labeled neurons versus for unlabeled neurons, , ); in control, no significant different between labeled or and unlabeled neurons was found ( for labeled neurons versus for unlabeled neurons). Thus, these results demonstrated that low frequency stimulation at ST36 selectively increased the NMDAR-mediated synaptic responses in gastric-projecting DMV neurons.
3.3. Electroacupuncture at ST36 Increases NMDAR-Mediated Synaptic Transmission through Presynaptic Regulation
It is well documented that excitatory amino acid inputs from the NTS mediate vagal gastric motor excitation via NMDA and kainite/AMPA receptors in vagal motor neurons [25, 26]. Having identified that low frequency stimulation at ST36 increased NMDAR-mediated EPSCs between NTS and DMV EPSC, we went on to identify the pre- or postsynaptic mechanism responsible for the impact of electroacupuncture at ST36 on synaptic transmission. At first, mEPSCs were recorded in acute brainstem slices from rats subjected to ST36 stimulation. Although mEPSC amplitude did not differ between retrogradely labeled and unlabeled DMV neurons ( pA versus pA, , ) (Figures 3(a)–3(d)), the frequency of mEPSC was significantly greater in labeled neurons (labeled neurons: Hz versus unlabeled neurons: Hz, , ) (Figures 3(a)–3(c), and 3(e)). In control animals without somatic stimulation, we did not observe any significant difference in either mEPSC amplitude or frequency between labeled and unlabeled DMV neurons (amplitude: pA and frequency: Hz for labeled neurons versus pA and Hz for unlabeled neurons, ) (Figures 3(a), 3(b), 3(d), and 3(e)).
In addition, we assessed the site of action by measuring the ratio of the amplitudes of two postsynaptic currents in DMV neurons using a paired-pulse protocol. By delivering paired-pulse (10 Hz) stimulation to presynaptic NTS, we consistently observed a substantial change in paired-pulse ratio (PPR) of NMDAR-mediated currents in labeled and unlabeled neurons. As shown in Figures 4(a) and 4(c), the PPR of NMDAR-mediated EPSCs recorded from the retrogradely labeled DMV neurons was significantly larger in ST36 group than that in control ( versus 0.71 + 0.02; , ). In fact, there was a paired-pulse facilitation in labeled neurons compared to paired-pulse depression in unlabeled neurons. For the ST36 group, there was also a significant difference between PPR of NMDAR-mediated EPSCs in labeled and unlabeled neurons ( for labeled neurons versus for unlabeled neurons, , ) (Figures 4(a) and 4(c)). By contrast, there was little changes in PPR of AMPAR-mediated EPSCs after ST36 stimulation, as the PPR recorded from labeled neuron in stimulated rats was not different with that either recorded from labeled neurons in the control group or unlabeled neurons in ST36 group ( for labeled neurons in ST36 group versus for labeled neurons in control; and for unlabeled neurons: , ) (Figures 4(a)–4(d)). Given that a PPR change is indicative of a presynaptic site of action , these data suggested that stimulating ST36 increased NMDAR-mediated synaptic transmission via a presynaptic mechanism.
3.4. Electroacupuncture at ST36 Inhibits Presynaptic μ-Opioid Receptors
Previous evidence indicates that increasing activity of the presynaptic μ-opioid receptors attenuates the excitatory synaptic transmission from the NTS to GI-projecting DMV neurons . Here we set out to detect whether stimulating ST36 can affect presynaptic μ-opioid receptors and hence increase NMDAR-mediated synaptic transmission. As shown in Figures 5(a) and 5(c), the NMDAR-mediated EPSCs in labeled neurons were significantly reduced by perfusion of the brain slice with a competitive agonist of μ-opioid receptors, D-Ala2, N-MePhe4, Gly5-ol-enkephalin (DAMGO) ( pA versus pA. , ), and the reduction in NMDAR-mediated EPSCs by DAMGO was reversed by 0.2 μm naloxonazine, a selective μ-opioid receptor antagonist ( pA, ). In addition, we found that the enhanced PPR by ST36 stimulation was abolished by DAMGO (stimulation: versus stimulation + DAMGO: . , -8), and reversed by naloxonazine (, , ) (Figures 5(b) and 5(d)). Taken together, these data suggested that low frequency stimulation at ST36 inhibits the presynaptic μ-opioid receptor.
3.5. Electroacupuncture at ST36 Increases NR2A-Containing NMDAR-Mediated Synaptic Transmission of Gastric-Projecting DMV Neurons
To further characterize the role of specific subunits of NMDAR in mediating regulation of gastric motility by stimulating ST36, we applied selective antagonists which block either NR2A or NR2B containing NMDARs during whole-cell recording in the retrograde labeling neurons. Figures 6(a) and 6(b) show that in the presence of a NR2A-specific antagonist, ((R)-((S)-1-(4-bromophenyl)-ethylamino)-(2,3-dioxo-1,2,3,4-tetrahydroquinoxalin-5-yl)-methyl)-phosphonic acid (NVP-AAM077) (0.4 μM), the facilitation of NMDAR-mediated EPSCs induced by ST36 stimulation in labeled neurons was abolished completely (stimulation: pA, ; NVP-AAM077: pA, ; ). Conversely, no significant difference was observed between pre- and postapplication of 3 μM ifenprodil, a NR2B antagonist  ( pA, ). Another NR2B-specific antagonist Ro25-6981 (0.5 μM)  also did not cause a significant change in evoked NMDAR-mediated EPSCs ( pA, ), suggesting that NR2A-containing NMDARs are essential for NMDAR-mediated increase of gastric motility by stimulating ST36.
3.6. NVP-AAM077 Microinjection Diminishes the Enhancement of Gastric Motility Induced by Electroacupuncture at ST36 in Anesthetized Rats and Transgenic Mice
To examine whether these findings for the role of NR2A-containing NMDARs observed in vitro could be reproduced in vivo, NVP-AAM077 (2 nL, 0.4 μM) was microinjected into DMV before ST36 stimulation in anesthetized rats. As shown in Figures 7(a) and 7(b), the increase of the intragastric pressure induced by stimulating ST36 was diminished significantly after microinjection of NVP-AAM077 (% versus %, , ). To further verify a specific role of NR2A in mediating the regulation of gastric motility by stimulating ST36, we performed the same stimulation protocol in both wild-type and NR2A knockout mice. As shown in Figures 7(c) and 7(d), low frequency stimulation at ST increased gastric motility in the wild-type littermates, but not in the NR2A knockout mice (%, versus %, , ), providing additional evidence that NR2A-containing NMDARs of DMV neurons are required for the increase of gastric motility induced by stimulating ST36.
In the present study, we discovered that NMDARs of gastric-projecting DMV neurons play a critical role in mediating the enhancement of gastric motility induced by electroacupuncture at ST36 in anesthetized rats. Stimulating ST36 enhances NMDAR-mediated synaptic transmission through inhibiting presynaptic μ-opioid receptors. We also determined that the enhancement of NR2A-containing NMDAR-mediated synaptic transmission between NTS and gastric-projecting DMV neurons is an absolute requirement for this potent regulation of gastric motility. Therefore, our study unveiled a novel molecular mechanism by which stimulating ST36 upregulates gastric motility via the vagal pathway.
Somatovisceral reflexes responsible for regulation of visceral organs are strongly associated with the effects of acupuncture. Application of acupuncture to the abdominal region inhibits gastric motility in anesthetized rats via a spinal reflex that activates sympathetic efferent nerve fibers, while stimulating a limb increases gastric motility via a supra-spinal reflex that activates vagal nerve fibers [19, 31, 32]. Here, we found that low frequency stimulation at ST36 can significantly increase gastric motility, but stimulating CV12 decreases gastric motility significantly. Our results are consistent with previous reports and provide strong support for the location specificity of somatic stimulation in regulating gastric motility.
It is well documented that somatic stimulation upregulates gastric motility through the vagal reflex pathway [5, 19]. However, little is known regarding the anatomic circuit and functional changes underlying the somatic stimulation induced regulation of gastric motility. In the vagal reflex pathway, DMV plays a pivotal role in controlling the motility of the GI tract, as it sends efferent projections to the GI tract. NTS neurons also regulate gastric motility by providing direct inhibitory and excitatory inputs to preganglionic parasympathetic neurons in the DMV. Based on previous studies in brainstem slice preparations, endogenously occurring glutamate and GABA are the major neurotransmitters controlling the excitability of DMV motor neurons , while their inhibitory and excitatory effects on the excitability of DMV neurons are mediated directly via activation of postsynaptic GABAa receptors and both NMDA- and non-NMDA-type glutamatergic receptors [26, 33, 34]. Our finding that the increase in intragastric pressure induced by low frequency stimulation at ST36 was diminished by NMDAR antagonist AP5 indicates that low frequency stimulation at ST36 upregulates gastric motility through the excitatory synaptic transmission between NTS and DMV, especially through NMDARs rather than non-NMDARs of DMV neurons.
The distinct distribution and morphology are characteristics of a subpopulation of DMV neurons that project to the stomach . Our finding that stimulating ST36 enhances NMDAR-mediated EPSCs specifically in the retrogradely labeled neurons suggests that NMDARs of gastric-projecting DMV neurons mediate the regulation of gastric motility by somatic stimulation. We also determined that the ST36 stimulation induced enhancement of NMDAR-mediated synaptic transmission in DMV neurons is through presynaptic regulation, and propose inhibition of presynaptic μ-opioid receptors as one of the potential mechanisms. This hypothesis is supported by previous observations that opioid peptides attenuate excitatory synaptic transmission to gastric-projecting DMV neurons via interactions with presynaptic μ-opioid receptors . In addition, opioid pathway may contribute to long-lasting effects of acupuncture on gastric motility . The current result that μ-opioid receptor agonist DAMGO inhibited EPSCs of the gastric-projecting DMV neurons also suggests that increasing NMDAR-mediated synaptic transmission may be attributed to the inhibition of presynaptic μ-opioid receptors. However, the data that low frequency stimulation at ST36 did not change AMPAR-mediated synaptic transmission implies that other mechanisms might be involved and also need to be clarified in the future.
In the present work, we demonstrate that NMDAR-mediated excitation of DMV neurons evoked by ST36 stimulation is primarily mediated by NR1/NR2A receptors, as NR2A preferential antagonist in vitro decreases NMDAR-mediated synaptic response and in vivo abolishes the increase of gastric motility induced by low frequency somatic stimulation. The observed involvement of NR2A receptors in NMDAR-mediated upregulation of gastric motility by low frequency stimulation at ST36 is in agreement with previous reports that, in the adult brainstem, NR2A is predominantly expressed among the four NR2 subunits [36, 37] and the functional change in NMDAR properties is correlated with an increase in the NR2A subunit ratio [37, 38].
To sum, our study establishes that low frequency somatic stimulation at ST36 enhances NMDAR-mediated synaptic transmission via suppressing presynaptic μ-opioid receptors, and in turn increases NR2A-containing NMDAR-mediated synaptic transmission in gastric-projecting DMV neurons. While future studies are needed to clarify how low frequency stimulation at ST36 inhibits presynaptic μ-opioid receptors and thus increases NMDAR-mediated synaptic transmission, our data provide an important insight into the mechanism for ST36 stimulation enhanced gastric motility. In the future, this finding may also help to develop treatment strategy for gastric motility disorders by an NR2A-containing NMDAR-based activation approach.
Conflict of Interests
No conflict of interests, financial or otherwise, is declared by the author(s).
The experiments were performed in the laboratories of H. Qiao and B. Zhu; X. Gao, H. Qiao, and B. Zhu made conception and design of research; X. Gao, Y. Qiao, B. Jia, X. Jing B. Cheng, and Q. Tan performed experiments; X. Gao, B. Cheng, L. Wen, and H. Qiao analyzed data; X. Gao, Y. Zhou, B. Zhu, and H. Qiao interpreted results of experiments; X. Gao, B. Zhu, and H. Qiao prepared figures; X. Gao, and H. Qiao drafted the manuscript; X. Gao, Y. Zhou, B. Zhu, and H. Qiao edited and revised the manuscript; X. Gao, B. Cheng, B. Jia, X. Jing, L. Wen, Q. Tan, Y. Zhou, B. Zhu, and H. Qiao approved the final version of the paper.
This work was supported by National Natural Science Foundation of China Grants to H. Qiao (nos. 30772706 and 81273831), X. Gao (no. 30371804) and X. Jing (no. 30873241), intramural program of China Academy of Chinese Medical Sciences Institute of Acupuncture and Moxibustion to H. Qiao (ZZ12006), and the National Basic Research Program of China Grant to B. Zhu (no. 2011CB505201) and X. Jing (no. 2010CB530507). The authors thank Matthew Davis for word polishing.
- X. Lin, J. Liang, J. Ren, F. Mu, M. Zhang, and J. D. Chen, “Electrical stimulation of acupuncture points enhances gastric myoelectrical activity in humans,” American Journal of Gastroenterology, vol. 92, no. 9, pp. 1527–1530, 1997.
- C. S. Chang, C. W. Ko, C. Y. Wu, and G. H. Chen, “Effect of electrical stimulation on acupuncture points in diabetic patients with gastric dysrhythmia: a pilot study,” Digestion, vol. 64, no. 3, pp. 184–190, 2001.
- H. Ouyang and J. D. Z. Chen, “Review article: therapeutic roles of acupuncture in functional gastrointestinal disorders,” Alimentary Pharmacology and Therapeutics, vol. 20, no. 8, pp. 831–841, 2004.
- T. Takahashi, “Acupuncture for functional gastrointestinal disorders,” Journal of Gastroenterology, vol. 41, no. 5, pp. 408–417, 2006.
- J. Yin and J. D. Z. Chen, “Gastrointestinal motility disorders and acupuncture,” Autonomic Neuroscience, vol. 157, no. 1-2, pp. 31–37, 2010.
- Y. Li, G. Tougas, S. G. Chiverton, and R. H. Hunt, “The effect of acupuncture on gastrointestinal function and disorders,” American Journal of Gastroenterology, vol. 87, no. 10, pp. 1372–1381, 1992.
- G. Lux, J. Hagel, P. Bäcker et al., “Acupuncture inhibits vagal gastric acid secretion stimulated by sham feeding in healthy subjects,” Gut, vol. 35, no. 8, pp. 1026–1029, 1994.
- H. Ouyang, J. Yin, Z. Wang, P. J. Pasricha, and J. D. Z. Chen, “Electroacupuncture accelerates gastric emptying in association with changes in vagal activity,” American Journal of Physiology, vol. 282, no. 2, pp. G390–G396, 2002.
- M. Tatewaki, M. Harris, K. Uemura et al., “Dual effects of acupuncture on gastric motility in conscious rats,” American Journal of Physiology, vol. 285, no. 4, pp. R862–R872, 2003.
- J. Chen, G. Q. Song, J. Yin, T. Koothan, and J. D. Z. Chen, “Electroacupuncture improves impaired gastric motility and slow waves induced by rectal distension in dogs,” American Journal of Physiology, vol. 295, no. 3, pp. G614–G620, 2008.
- K. N. Browning, W. E. Renehan, and R. A. Travagli, “Electrophysiological and morphological heterogeneity of rat dorsal vagal neurones which project to specific areas of the gastrointestinal tract,” Journal of Physiology, vol. 517, Part 2, pp. 521–532, 1999.
- R. A. Gillis, J. A. Quest, F. D. Pagani, et al., “Control centers in the central nervous system for regulating gastrointestinal motility,” in Comprehensive Physiology, R. Terjung, Ed., pp. 621–683, Wiley Online Library, 2011.
- R. A. Travagli, G. E. Hermann, K. N. Browning, and R. C. Rogers, “Brainstem circuits regulating gastric function,” Annual Review of Physiology, vol. 68, pp. 279–305, 2006.
- H. Gao and B. N. Smith, “Tonic GABAa receptor-mediated inhibition in the rat dorsal motor nucleus of the vagus,” Journal of Neurophysiology, vol. 103, no. 2, pp. 904–914, 2010.
- H. E. Raybould, L. J. Jakobsen, D. Novin, and Y. Tache, “TRH stimulation and L-glutamic acid inhibition of proximal gastric motor activity in the rat dorsal vagal complex,” Brain Research, vol. 495, no. 2, pp. 319–328, 1989.
- H. S. Feng, R. B. Lynn, J. Han, and F. P. Brooks, “Gastric effects of TRH analogue and bicuculline injected into dorsal motor vagal nucleus in cats,” American Journal of Physiology, vol. 259, no. 2, pp. G321–G326, 1990.
- R. A. Travagli, R. A. Gillis, and S. Vicini, “Effects of thyrotropin-releasing hormone on neurons in rat dorsal motor nucleus of the vagus, in vitro,” American Journal of Physiology, vol. 263, no. 4, pp. G508–G517, 1992.
- R. J. Washabau, M. Fudge, W. J. Price, and F. C. Barone, “GABA receptors in the dorsal motor nucleus of the vagus influence feline lower esophageal sphincter and gastric function,” Brain Research Bulletin, vol. 38, no. 6, pp. 587–594, 1995.
- Y. Q. Li, B. Zhu, P. J. Rong, H. Ben, and Y. H. Li, “Neural mechanism of acupuncture-modulated gastric motility,” World Journal of Gastroenterology, vol. 13, no. 5, pp. 709–716, 2007.
- X. Y. Gao, S. P. Zhang, B. Zhu, and H. Q. Zhang, “Investigation of specificity of auricular acupuncture points in regulation of autonomic function in anesthetized rats,” Autonomic Neuroscience, vol. 138, no. 1-2, pp. 50–56, 2008.
- S. Cheng, Chinese Acupuncture and Moxibustion, Foreign Language Press, Beijing, China, 1996.
- K. N. Browning, A. E. Kalyuzhny, and R. A. Travagli, “μ-opioid receptor trafficking on inhibitory synapses in the rat brainstem,” Journal of Neuroscience, vol. 24, no. 33, pp. 7344–7352, 2004.
- Z. K. Krowicki, K. A. Sharkey, S. C. Serron, N. A. Nathan, and P. J. Hornby, “Distribution of nitric oxide synthase in rat dorsal vagal complex and effects of microinjection of nitric oxide compounds upon gastric motor function,” The Journal of Comparative Neurology, vol. 377, pp. 49–69, 1997.
- R. C. Rogers, G. E. Hermann, and R. A. Travagli, “Brainstem pathways responsible for oesophageal control of gastric motility and tone in the rat,” Journal of Physiology, vol. 514, no. 2, pp. 369–383, 1999.
- P. J. Hornby, “Receptors and transmission in the brain-gut axis. II. Excitatory amino acid receptors in the brain-gut axis,” American Journal of Physiology, vol. 280, no. 6, pp. G1055–G1060, 2001.
- X. Zhang and R. Fogel, “Glutamate mediates an excitatory influence of the paraventricular hypothalamic nucleus on the dorsal motor nucleus of the vagus,” Journal of Neurophysiology, vol. 88, no. 1, pp. 49–63, 2002.
- K. N. Browning and R. A. Travagli, “The peptide TPH uncovers the presence of presynaptic 5-HT1A receptors via activation of a second messenger pathway in the rat dorsal vagal complex,” Journal of Physiology, vol. 531, no. 2, pp. 425–435, 2001.
- K. N. Browning, A. E. Kalyuzhny, and R. A. Travagli, “Opioid peptides inhibit excitatory but not inhibitory synaptic transmission in the rat dorsal motor nucleus of the vagus,” Journal of Neuroscience, vol. 22, no. 8, pp. 2998–3004, 2002.
- Y. Liu, T. P. Wong, M. Aarts et al., “NMDA receptor subunits have differential roles in mediating excitotoxic neuronal death both in vitro and in vivo,” Journal of Neuroscience, vol. 27, no. 11, pp. 2846–2857, 2007.
- V. Mutel, D. Buchy, A. Klingelschmidt et al., “In vitro binding properties in rat brain of [3H] Ro 25-6981, a potent and selective antagonist of NMDA receptors containing NR2B subunits,” Journal of Neurochemistry, vol. 70, no. 5, pp. 2147–2155, 1998.
- A. Sato, Y. Sato, A. Suzuki, and S. Uchida, “Neural mechanisms of the reflex inhibition and excitation of gastric motility elicited by acupuncture-like stimulation in anesthetized rats,” Neuroscience Research, vol. 18, no. 1, pp. 53–62, 1993.
- E. Noguchi, “Acupuncture regulates gut motility and secretion via nerve reflexes,” Autonomic Neuroscience, vol. 156, no. 1-2, pp. 15–18, 2010.
- A. Willis, M. Mihalevich, R. A. Neff, and D. Mendelowitz, “Three types of postsynaptic glutamatergic receptors are activated in DMNX neurons upon stimulation of NTS,” American Journal of Physiology, vol. 271, no. 6, pp. R1614–R1619, 1996.
- D. L. Broussard, H. Li, and S. M. Altschuler, “Colocalization of GABA(A) and NMDA receptors within the dorsal motor nucleus of the vagus nerve (DMV) of the rat,” Brain Research, vol. 763, no. 1, pp. 123–126, 1997.
- M. Tatewaki, M. Harris, K. Uemura et al., “The stimulatory effects of acupuncture on gastric motility is mediated via vagal cholinergic and opioid pathways in conscious rats,” Gastroenterology, vol. 124, Supplement 1, pp. A669–A670, 2003.
- H. Monyer, R. Sprengel, R. Schoepfer et al., “Heteromeric NMDA receptors: molecular and functional distinction of subtypes,” Science, vol. 256, no. 5060, pp. 1217–1221, 1992.
- J. Nabekura, T. Ueno, S. Katsurabayashi, A. Furuta, N. Akaike, and M. Okada, “Reduced NR2A expression and prolonged decay of NMDA receptor-mediated synaptic current in rat vagal motoneurons following axotomy,” Journal of Physiology, vol. 539, no. 3, pp. 735–741, 2002.
- S. Vicini, J. F. Wang, J. H. Li et al., “Functional and pharmacological differences between recombinant N- methyl-D-aspartate receptors,” Journal of Neurophysiology, vol. 79, no. 2, pp. 555–566, 1998.