Regulatory effects of anandamide on intracellular Ca2+concentration increase in trigeminal ganglion neurons

Yi Zhang, Hong Xie, Gang Lei, Fen Li, Jianping Pan, Changjin Liu, Zhiguo Liu, Lieju Liu, Xuehong Cao,

1 Department of Anesthesiology, Tongji Hospital Af fi liated to Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei Province, China

2 Jingzhou Central Hospital, Jingzhou, Hubei Province, China

3 Department of Physiology, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei Province, China

4 Department of Bioengineering, Wuhan Institute of Engineering, Wuhan, Hubei Province, China

Regulatory effects of anandamide on intracellular Ca2+concentration increase in trigeminal ganglion neurons

Yi Zhang1, Hong Xie2, Gang Lei3, Fen Li3, Jianping Pan3, Changjin Liu3, Zhiguo Liu4, Lieju Liu4, Xuehong Cao3,4

1 Department of Anesthesiology, Tongji Hospital Af fi liated to Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei Province, China

2 Jingzhou Central Hospital, Jingzhou, Hubei Province, China

3 Department of Physiology, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei Province, China

4 Department of Bioengineering, Wuhan Institute of Engineering, Wuhan, Hubei Province, China

Xuehong Cao, M.D., Ph.D.,

Department of Physiology, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, Hubei Province, China; Department of

Bioengineering, Wuhan Institute of

Engineering, Wuhan 430023, Hubei

Province, China, caoxuehong@gmail.com. Lieju Liu, M.D., Department of

Bioengineering, Wuhan Institute of

Engineering, Wuhan 430023, Hubei

Province, China, liejuliu@gmail.com.

Activation of cannabinoid receptor type 1 on presynaptic neurons is postulated to suppress neurotransmission by decreasing Ca2+influx through high voltage-gated Ca2+channels. However, recent studies suggest that cannabinoids which activate cannabinoid receptor type 1 can increase neurotransmitter release by enhancing Ca2+influx in vitro. The aim of the present study was to investigate the modulation of intracellular Ca2+concentration by the cannabinoid receptor type 1 agonist anandamide, and its underlying mechanisms. Using whole cell voltage-clamp and calcium imaging in cultured trigeminal ganglion neurons, we found that anandamide directly caused Ca2+in fl ux in a dose-dependent manner, which then triggered an increase of intracellular Ca2+concentration. The cyclic adenosine and guanosine monophosphate-dependent protein kinase systems, but not the protein kinase C system, were involved in the increased intracellular Ca2+concentration by anandamide. This result showed that anandamide increased intracellular Ca2+concentration and inhibited high voltage-gated Ca2+channels through different signal transduction pathways.

nerve regeneration; trigeminal ganglion; neurons; endocannabinoids; anandamide; cannabinoid receptor type 1; voltage-dependent calcium channels; vanilloid receptor; patch-clamp technique; calcium; cyclic adenosine monophosphate protein kinase; protein kinase C; NIH grant; neural regeneration

Funding: This work was supported by NIH, grant No. GM-63577; NNSF, grant No. 30571537, No. 30271500; the National Natural Science Foundation of China, No. 30271500, 30571537 and 81370246. 2010 National Clinical Key Disciplines Construction Grant from the Ministry of Health of the People’s Republic of China.

Zhang Y, Xie H, Lei G, Li F, Pan JP, Liu CJ, Liu ZG, Liu LJ, Cao XH. Regulatory effects of anandamide on intracellular Ca2+concentration increase in trigeminal ganglion neurons. Neural Regen Res. 2014;9(8)：878-887.

Introduction

N-arachidonoylethanolamine (anandamide) is referred to as the first ‘endocannabinoid’ described, and anandamide signaling has been reported to be an inhibitor of axon regeneration. Anandamide acts primarily on cannabinoid receptor type 1 (CB1)[1], cannabinoid receptor type 2 (CB2)[2], and ionotropic receptors, including the transient receptor potential (TRP) vanilloid type 1 (TRPV1)[3-5], TRP ankyrin type 1 (TRPA1) and TRP melastatin type 8 (TRPM8) channels[6]. Anandamide can also directly modulate various other ion channels[5,7-10].

CB1and CB2are members of the subfamily of G-protein-coupled receptors and predominantly couple to Gi/o[1,11]to produce multiple cellular effects, such as the inhibition of adenylate cyclase and of voltage-gated calcium channels[12-14], regulation of potassium currents[15-17], and increase of Ca2+in fl ux via Gs[18]and Gq

[19]. TRPV1 is a polymodal sensor of noxious stimuli including heat, hydrogen ions and capsaicin[20]. CB1

[21]and TRPV1, but not CB2[21]are expressed in presynaptic primary neurons such as those in the trigeminal ganglion. CB1is localized to presynaptic nerve terminals[22]and contributes to the regulation of neuronal excitability and neurotransmitter release by modulating Ca2+signals. TRPV1 activation causes Ca2+to enter into the cell and promotes neurotransmitter release. Studies have demonstrated that anandamide can activate TRPV1 by binding to cytosolic sites[23]. The co-expression and close distribution of CB1and TRPV1 in primary sensory neurons[24-27]allows cross-talk between these two receptors, which further complicates the role of anandamide in nociception and antinociception. The present study will determine which receptor contributes to the effect of low and high concentrations of anandamide in small trigeminal ganglion neurons.

Figure 1 Anandamide-evoked currents in rat trigeminal ganglion neurons.

Figure 2 Dose-dependent anandamide-evoked currents (nA) in trigeminal ganglion neurons, measured by the voltage-ramp method from -60 to +60 mV.

It is a widely accepted general hypothesis that endocannabinoids inhibit neurotransmitter release from primary afferent neurons by reducing Ca2+influx via an inhibitory action on high voltage-gated Ca2+channels. This hypothesis is supported by evidence that CB1activation by anandamide on primary nociceptive neurons causes antinociception by reducing high voltage-activated Ca2+channel activity[12-14]and Ca2+in fl ux[28], thus inhibiting neurotransmission. In contrast, some studies suggest that cannabinoids can promote Ca2+influx and hence increase neurotransmitter release in vitro[19,25,29-31]. How endocannabinoids may cause such opposing effects in intracellular Ca2+concentration and neuron excitability is unclear. High voltage-gated calcium channels and ligand-gated channels, two important contributors to intracellular Ca2+concentration, will also be investigated. The present study tests the above hypothesis by determining the effect of anandamide on high voltage-activated Ba2+currents (IHVA), Ca2+in fl ux and intracellular Ca2+concentration, as well as the underlying mechanisms, in small trigeminal ganglion neurons.

Results

Anandamide-evoked inward currents

Whole-cell patch-clamp recordings were carried out in rat trigeminal ganglion neurons with bath perfusion of 0.1, 0.3, 1, 3, 10, 30 and 100 μmol/L anandamide at a range of holding potentials from -60 mV to +60 mV (Figure 1). Reversal potentials were around 0 mV. Anandamide-evoked inward and outward currents at holding potentials of -60 mV and +60 mV, respectively, were dose-dependent (Figure 2).

Inhibition ofIHVAby anandamide

Bath application of anandamide (0.001, 0.01, 0.1, 1, 10, 30 μmol/L) inhibited IHVAin a concentration-dependent manner, by 4.62 ± 0.88%, 6.24 ± 2.57%, 18.17 ± 0.99%, 31.30 ± 3.21%, 64.73 ± 1.95% and 55.19 ± 2.06%, respectively (n = 4-11). The effect of anandamide was partially reversed after washout. The Hill equation was applied to the dose-response curve and revealed that the half-maximal inhibitory concentration (IC50) of anandamide was 0.92 μmol/L. To confirm whether other CB1agonists mimicked the inhibition of anandamide, we tested the effect of WIN 55,212-2 (10 μmol/L) on IHVA. The inhibition of IHVAby 10 μmol/L WIN 55,212-2 was 55.78 ± 6.07%. Anandamide at 1 μmol/L reduced current amplitudes (Figure 3A, B) but did not cause a significant shift of the activation curve (Figure 3C). However, a hyperpolarization shift of almost 14 mV (n = 8; P ＜ 0.05) was ob-served in the h-in fi nity curve (Figure 3E).

Figure 3 Inhibition of high voltage-activated Ca2+currents (IHVA) in rat trigeminal ganglion neurons by exposure to anandamide (1 µmol/L) for 3 minutes.

Roles of cannabinoid and vanilloid receptors in the inhibition ofIHVAby anandamide

Since anandamide activates TRPV1, CB1and CB2receptors, we tested whether capsazepine, AM251 and AM630, selective antagonists at the three receptors, respectively, could reverse the effect of anandamide on IHVA. Capsazepine (10 μmol/L), AM251 (10 μmol/L), AM630 (10 μmol/L), or anandamide (1 and 10 μmol/L) were added to the bath solution during whole-cell patch clamp recordings in rat trigeminal ganglion neurons. First, we examined how pre-incubation of the cells for 3 minutes with capsazepine, a competitive antagonist at TRPV1, would affect the inhibition induced by anandamide (Figure 4A, D). Pre-incubation with capsazepine did not affect the inhibition of IHVAby 1 μmol/L anandamide (n = 10, P ＞ 0.05), but abolished the effect of 10 μmol/L anandamide (n = 12, P ＜ 0.05). These data indicate that TRPV1 activation is involved in the inhibition of IHVAby high-concentration anandamide. AM251 was co-applied with anandamide (1 or 10 μmol/L) (Figure 4B, E). Low-dose (n = 7, P ＜ 0.05) and high-dose (n = 4, P ＜ 0.05) anandamide-induced inhibition was reversed by AM251 (Figure 4G), indicating that activation of CB1is essential for the negative modulation of IHVAby anandamide in rat trigeminal ganglion neurons.

Pre-incubation for 3 minutes with AM630 did not affect IHVAinhibition induced by 1 μmol/L (Figure 4C, G; P ＞ 0.05) or 10 μmol/L (Figure 4F, G; P ＞ 0.05) anandamide, indicating a lack of CB2 receptors in rat trigeminal ganglion neurons[21].

Inhibition ofIHVAby capsaicin

As described above, inhibition of IHVAby high-concentration anandamide was reversed by the TRPV1 antagonist capsazepine, suggesting that TRPV1 is involved in this effect. We further tested whether IHVAcould be directly inhibited by the TRPV1 agonist, capsaicin. Capsaicin and capsazepine were applied by bath perfusion. IHVAwas reversibly inhibited by capsaicin in a dose-dependent manner (Figure 5). Similar to the effect observed with high-concentration anandamide, the decrease in IHVAby capsaicin was reversed by 10 μmol/L capsazepine. In addition, IHVAwas not inhibited by 10 μmol/L capsazepine (Figure 6).

Characterization of signal transduction pathways mediating the inhibition ofIHVAviacannabinoid type-1 receptor activation by low-concentration anandamide

Three important signal transduction systems were examined using speci fi c agonists and antagonists to test whether thesesystems participated in the inhibition of IHVAby CB1 receptors activated by 1 μmol/L anandamide.

Figure 4 Cannabinoid and TRPV1 receptor involvement in the inhibition of high voltage-activated Ba2+currents (IHVA) by 1 and 10 µmol/L anandamide in rat trigeminal ganglion neurons.

Whole-cell patch clamp measurements in trigeminal ganglion neurons revealed that application of 1 μmol/L KT5720, an inhibitor of cyclic adenosine monophosphate -dependent protein kinase A, significantly attenuated the inhibition of IHVAby 1 μmol/L anandamide (Figure 7). Incubation with an antagonist of protein kinase C, bisindolylmaleimide (1 μmol/L for 10 minutes) and an inhibitor of cyclic guanosine monophosphate (cGMP)-dependent protein kinase, Rp-8-Br-cGMP (1 μmol/L for 10 minutes) also signi fi cantly attenuated anandamide-induced inhibition of IHVA.

Anandamide increased intracellular Ca2+concentrationviaa direct in fl ux of extracellular calcium into rat trigeminal ganglion neurons

Calcium imaging was used to examine the effect of anandamide on intracellular Ca2+concentration in the presence of solutions containing either 0 or 2 mmol/L Ca2+(Figure 8A). In the absence of extracellular calcium (buffered by 10 mmol/L ethylene glycol bis(alpha-aminoethyl ether)-N,N′-tetraacetic acid to decrease extracellular Ca2+concentrations), the rise in intracellular Ca2+concentration induced by anandamide was notably decreased (Figure 8B; anandamide([Ca2+]+): 20.33 ± 2.10%, n = 19; anandamide([Ca2+]-): 4.22 ± 1.06%, n = 48; P ＜ 0.01). Thus, the anandamide-induced rise in intracellular Ca2+concentration is dependent on Ca2+in fl ux from the extracellular space.

Cannabinoid / vanilloid type-1 receptor involvement in the mechanism underlying increased intracellular Ca2+concentration evoked by anandamide

Because AM630 had no effect on the inhibition of anandamide on IHVA, in the present test only AM251 and capsazepine were used, to determine whether they would affect the increase of anandamide on the intracellular Ca2+concentration, using calcium imaging. The 1 μmol/L anandamide-induced rise in intracellular Ca2+concentration was abolished by co-application with 10 μmol/L AM251 (Figure 8C), while lower doses of AM251 (1 and 3 μmol/L) facilitated the in-crease of 1 μmol/L anandamide (Figure 8C). This suggests that co-incubation with 1 μmol/L anandamide and low-dose AM251 facilitates intracellular Ca2+in fl ux via TRPV1 while at the same time inhibiting it via CB1receptors.

Figure 5 Cannabinoid andtransient receptor potential (TRP) vanilloid type 1receptor involvement in the inhibition of high voltage-activated Ca2+currents (IHVA) by 1 and 10 µmol/L anandamide in rat trigeminal ganglion neurons.

Figure 6 Capsazepine (CPZ) inhibited the capsaicin-induced decrease of Ca2+current (IHVA) in trigeminal ganglion neurons.

Figure 7 The role of different signaling pathways in the inhibition of 1 µmol/L anandamide on Ca2+currents (IHVA) in rat trigeminal ganglion neurons.

Similar to the effect of 10 μmol/L anandamide observed on IHVA, the increase in intracellular Ca2+concentration was also blocked by both AM251 and capsazepine (Figure 8C), indicating that different receptors participate in the responses of intracellular Ca2+concentration to low and high concentrations of anandamide in rat trigeminal ganglion neurons.

Signaling pathways mediating the increase in intracellular Ca2+concentration after cannabinoid receptor activation by low-concentration anandamide

Calcium imaging was used to evaluate the possible contribution of cAMP-dependent protein kinase, protein kinase C, and cGMP-dependent protein kinase systems to the observed effect on intracellular Ca2+concentration after CB1 activation. The effects of 1 μmol/L anandamide on intracellular Ca2+concentrations in trigeminal ganglion neurons pre-treated with KT5720 (an inhibitor of cAMP-dependent protein kinase), staurosporine (an inhibitor of protein kinase C) and KT5823 (an inhibitor of cGMP-dependent protein kinase) were investigated. Figure 8D showed that staurosporine (10 μmol/L for 15 minutes) had no effect on the rise in intracellular Ca2+concentration after anandamide application (n = 13, P ＞ 0.05). Pretreatment with KT5720 (10 μmol/L for 10 minutes) and KT5823 (10 μmol/L for 10 minutes) markedly attenuated the response of 1 μmol/L anandamide (Figure 8D). These data suggest that the cAMP-dependent protein kinase and cGMP-dependent protein kinase systems, but not the protein kinase C system, are involved in the increase in intracellular Ca2+concentration with 1 μmol/L anandamide.

Discussion

Figure 8 Effects of anandamide on intracellular Ca2+concentration ([Ca2+]i) in rat trigeminal ganglion neurons.

It is well established that presynaptic CB1receptor activation has an inhibitory role on high voltage-activated Ca2+channels, resulting in a decrease in Ca2+in fl ux and an inhibition of neurotransmitter release. In contrast, results from the present study show that anandamide causes a dose-dependent elevation of intracellular Ca2+concentration, triggered by anandamide-evoked currents, but not modulation of high voltage-activated Ca2+channels by anandamide. Furthermore, anandamide-induced inhibition of the high voltage-activated Ca2+channels and the increase in the intracellular Ca2+concentration are demonstrated to be two separate events differing in signal transduction pathways but having similar effects via the same receptors. Thus, our data suggest that anandamide, as an endocannabinoid, might exert an excitatory effect by increasing intracellular Ca2+concentration, triggered by anandamide-evoked currents.

It has been well documented that the endocannabinoid anandamide, and its synthetic analogue methanandamide, have dual effects. At low concentrations, anandamide selectively activates CB1receptors, while at high concentrations it activates excitatory TRPV1 receptors[24]. In pre-contracted strips of rat hepatic artery, rat small mesenteric artery and guinea-pig basilar artery, vasorelaxation induced by high-concentration anandamide is antagonized by the TRPV1 antagonist capsazepine, but not by the CB1receptor antagonist SR141716 (0.3 μmol/L)[4]. Further evidence indicates that anandamide not only acts on transfected TRPV1 receptors to produce membrane currents and increase the intracellular Ca2+concentration[4,32], but also acts on naturally-expressed TRPV1 receptors in neonatal rat dorsal root ganglia to produce membrane currents[33]. Here, we present strong evidence that anandamide selectively activates the CB1receptor at low concentrations in small trigeminal ganglion neurons. At high concentrations, anandamide activates both CB1and TRPV1 receptors, inhibiting IHVA. To confirm that high-concentration anandamide inhibited IHVAvia TRPV1 receptor activation, we compared the effects of high-concentration anandamide and the TRPV1 agonist capsaicin. We found that the inhibition induced by high-concentration anandamide and by capsaicin shared similar characteristics. First, both inhibited IHVAin a dose-dependent manner and were reversed by the TRPV1 receptor antagonist capsazepine. Second, like capsaicin, high-concentration anandamide induced inward currents in cultured trigeminal ganglion neurons. Similar to capsaicin-induced inward current, thereversal potential of anandamide-induced current was also around 0 mV. Anandamide had different effects at low and high concentration via the activation of different receptors. By comparing the contribution of CB1and TRPV1 activation on anandamide-induced increases in intracellular Ca2+concentration, we conclude that anandamide-induced inhibition of high voltage-activated Ca2+channels and an increase in intracellular Ca2+concentration have the same dual effects as activation of the receptor pathway.

Inhibition of high voltage-activated Ca2+channels and modulation of Ca2+influx are important for neuronal activity and neurotransmitter release induced by endocannabinoids. However, evidence also suggests that cannabinoids can couple to Gs[18]and Gq[19]and activate TRPV1 receptors to increase Ca2+in fl ux. In addition, the response of cannabinoids on intracellular Ca2+concentration differs across cell types[34]. To elucidate the complex mechanisms underlying the intracellular Ca2+response, we further tested the effect of anandamide on intracellular Ca2+concentration. We found that anandamide increased intracellular Ca2+and simultaneously inhibited IHVAin the same population of trigeminal ganglion neurons, providing strong evidence that an increase in the intracellular Ca2+concentration is not due to IHVA. We found that anandamide had dual effects on the inhibition of IHVAand elevation of intracellular Ca2+concentration. However, by comparing the contribution of second messenger system, we found that cAMP- and cGMP-dependent protein kinase antagonists both reversed the anandamide-induced increase in intracellular calcium concentration and IHVAinhibition. Application of a protein kinase C antagonist reversed the inhibition of IHVAbut the anandamide-induced increase in intracellular Ca2+concentration was not blocked. From this, we can conclude that the increase in intracellular Ca2+concentration and the IHVAinhibition observed with anandamide are separate processes that share the same receptors but differ in intracellular signal transduction pathways.

CB1receptor activation by endocannabinoids has been mostly reported to cause depression of neuronal excitability and neurotransmitter release in presynaptic primary neurons[10,13,25,28,35-36]. Accumulating evidence indicates that cannabinoids may contribute to the potentiation of neurotransmission. Endocannabinoid release potentiates synaptic transmission via CB1receptor activation and dopamine release in the gold fi sh Mauthner cell[37]. Moreover, endocannabinoids may potentiate hippocampal synaptic transmission via astrocytic CB1activation[30]. In the suprachiasmatic nucleus, CB1receptor activation can increase excitability of circadian clock neurons[38]. It is widely accepted that CB1receptor activation suppresses neurotransmission by inhibiting high voltage-activated Ca2+channels, and decreases Ca2+in fl ux. In contrast to this general hypothesis, we found that endocannabinoids caused elevation of the intracellular Ca2+concentration in trigeminal ganglion neurons, which was triggered by endocannabinoid-evoked inward current around the resting membrane potential (-60 mV). Furthermore, endocannabinoid-induced increase in intracellular Ca2+concentration and decrease of high voltage-activated Ca2+channels were two independent events, which had the same dual effects via similar receptor pathways, but differed in the second messenger transduction pathway. Thus, our results suggest that presynaptic endocannabinoid release might potentiate neurotransmission via endocannabinoid-evoked current, increased Ca2+in fl ux, and increased intracellular Ca2+concentration.

In summary, anandamide dose-dependently causes an increase in intracellular Ca2+concentration, mediated by Ca2+influx via anandamide-evoked currents, but not high voltage-activated Ca2+channels. In the same population of trigeminal ganglion neurons, CB1receptor activation-induced inhibition of IHVAand increase in high voltage-activated Ca2+channels are two separate processes that share the same (CB1) receptors, but differ in signal transduction pathway. Thus, the effects of anandamide on high voltage-activated Ca2+channels ultimately depend on the balance between the increased Ca2+in fl ux via anandamide-evoked currents and inhibition of high voltage-activated Ca2+channels, suggesting a complex role of anandamide on inhibitory or excitatory neuromodulation. Contrary to the general hypothesis of endocannabinoid depression on neurotransmission, this study elucidates possible mechanisms underlying endocannabinoid-induced potentiation of neurotransmission via Ca2+signaling modulation.

Materials and Methods

Design

A cytological in vitro study.

Time and setting

All data were collected at the Departments of Pharmacology and Physiology, Tongji Medical College, Huazhong University of Science and Technology in China from September 2003 to April 2008. Data analysis and manuscript writing were performed at Baylor Medical College, USA, from April 2011 to October 2012.

Materials

180 male Sprague-Dawley rats weighing 180-200 g and aged 6-8 weeks were used. All animal protocols were approved by the faculty of Laboratory Animal Science, Huazhong University of Science and Technology (license No. SYXK (E) 2009-0049). All the experiments followed the Guidance Suggestions for the Care and Use of Laboratory Animals, formulated by the Ministry of Science and Technology of China[39].

Methods

Cell dissociation

Trigeminal ganglion neurons from Sprague-Dawley rats were cultured as described previously[40]. Brie fl y, trigeminal ganglia were dissected aseptically and washed with cold (4°C) modified Hank’s balanced salt solution containing NaCl 130 mmol/L, KCl 5 mmol/L, KH2PO40.3 mmol/L, NaHCO34.0 mmol/L, NaH2PO40.3 mmol/L, D-glucose 5.6 mmol/L, and ethylene glycol bis(alpha-aminoethyl ether)-N, N′-tetraacetic acid 10 mmol/L, hydroxyethyl piperazine ethanesulfonic acid 10 mmol/L, at pH 7.4. The ganglia were chopped into small pieces, and then incubated in 3 mL modi fi ed Hank’s solution with 0.1% collagenase (type XI-S)for 20-40 minutes at 37°C. Individual cells were dissociated by triturating them through a fi re-polished glass pipette, followed by incubating with 10 μg/mL DNase I (type lV) in F12 medium (Life Technologies, Gaithersburg, MD, USA) for 10 minutes at 37°C, before centrifuging for 5 minutes at 1,000 r/min. After centrifuging three times, the cells were cultured in F12 supplemented with 10% fetal bovine serum. The cells were planted on poly-D-lysine pre-coated glass coverslips (15 mm diameter) and cultured no more than 12 hours at 37°C in a water saturated atmosphere with 5% CO2.

Patch-clamp recording

The cells were placed in a recording chamber mounted on an inverted microscope (Leica Inc., Solms, Germany) and perfused with extracellular solution at room temperature (21-22°C). Whole-cell patch-clamp experiments were carried out using an Axopatch 200B amplifier (Axon Instruments, Foster City, CA, USA) and the output was digitized with a Digidata 1332A converter (Axon Instruments) and program pCLAMP 9.02 (Axon Instruments). Data were acquired at a sampling rate of 2 KHz. Cell membrane capacitance and series resistance were measured and compensated (＞ 90%). Data obtained from neurons in which uncompensated series resistance resulted in voltage-clamp errors ＞ 5 mV were not taken into further analysis. The cell diameters were measured with a calibrated eyepiece under phase contrast illumination.

The resistance of the microelectrode was 2-4 MΩ when filled with the pipette solution. The microelectrode was made from G85150T-4 glass pipettes (Warner Instruments Inc., Hamden, CT, USA). The external solution contained Choline-Cl 110 mmol/L, TEACl 20 mmol/L, BaCl210 mmol/L, MgCl22.0 mmol/L, hydroxyethyl piperazine ethanesulfonic acid 10 mmol/L, and D-glucose 20 mmol/L, adjusted to pH 7.4 with CsOH. Ba2+was used as the charge carrier when recording IHVA. Ba2+was replaced by Ca2+when recording anandamide-evoked currents. The pipette solution contained CsCl 120 mmol/L, CaCl20.1 mmol/L, MgCL22.0 mmol/L, ethylene glycol bis(alpha-aminoethyl ether)-N, N′-tetraacetic acid 10.0 mmol/L, hydroxyethyl piperazine ethanesulfonic acid 10.0 mmol/L and Tris-ATP 5.0 mmol/L, pH adjusted to 7.2 with CsOH. Small-sized cells were selected to perform the further experiments.

The volume of the recording chamber was about 1 mL and the local superfusion rate was 1 mL/min.

Calcium imaging

Drug-induced changes of high voltage-activated Ca2+channels were measured using a confocal laser scanning imaging system (Fluoview FV500, Olympus, Tokyo, Japan). The trigeminal ganglion cells on glass cover slips were loaded with Fluo 2-AM by incubation with 1-5 μmol/L Fluo 2-AM in standard external solution and were maintained in the dark for 30-40 minutes. The standard external solution contained NaCL 140.0 mmol/L, KCL 5.0 mmol/L, CaCL22.0 mmol/L, MgCL21.0 mmol/L, glucose 10.0 mmol/L and hydroxyethyl piperazine ethanesulfonic acid 10.0 mmol/L, pH adjusted to 7.4 with NaOH. Ca2+-free medium solution was identical except for the 2.0 mmol/L Ca2+and additional 10 mmol/L ethyleneglycol bis(alpha-aminoethyl ether)-N, N′-tetraacetic acid to lower extracellular Ca2+concentration. Small-sized trigeminal ganglion neurons (＜ 33 μmol/L) were selected to perform the further experiments.

Data analysis

The data were analyzed using pCLAMP 9.02 (Axon Instruments) and Sigmaplot 11.0 software (Systat Software Inc., San Jose, CA, USA). The amplitude of IHVAwas calculated as the peak current. Voltage-dependent activation for the study of changes on IHVAwas measured by a series of depolarized pulses (450 ms) from -50 mV to +40 mV, stepping by 10 mV with interval time of 5 seconds, at a holding potential of -80 mV. We fi tted a Boltzmann function to the voltage-dependent activation curves, that is G /Gmax=1/[1+exp (V0.5-Vm)/k], where Gmaxis the maximum conductance, V0.5is the membrane potential at which 50% of activation was observed, and k is the slope of the function. Voltage-dependent inactivation was measured by a two pulse protocol in which the precondition pulses (3 seconds) ranged from -80 to +20 in 10 mV increments; following test pulse (200 millsecords) was +10 mV with an internal time of 6 seconds. The Boltzmann function was also fitted to the h-infinity curve, that is, I/ Imax=1/[1+exp(V0.5-Vm)/k], where V0.5is the membrane potential at which 50% of inactivation was observed, and k is the slope of the function. The dose-response curve was fi tted by the Hill equation, in which, Ipeak=Ipeakmax/[1+(IC50/C)n], with IC50as the concentration producing 50% inhibition and n as the Hill coef fi cient.

Statistical analysis

Data were presented as mean ± SEM. For all experiments, data were examined for Gaussian distribution fi rst, and then analyzed for statistical significance using the paired or unpaired t-test and one-way analysis of variance by using Sigma plot 11.0 software (Systat Software Inc.). A value of P ＜ 0.05 was considered statistically signi fi cant.

Author contributions:Liu LJ and Cao XH conceived the study and developed crucial proof-of-concept studies. Zhang Y contributed to data analysis and revised manuscript. Xie H performed calcium imaging. Lei G, Li F and Pan JP performed cell dissociation and data analysis. Liu ZG contributed to revised manuscript. Liu CJ also contributed to revised manuscript and study design. All authors approved the final version of the paper.

Con fl icts of interest:None declared.

Peer review:This study systemically determines how anandamide affects Ca2+signaling and underlying mechanisms in small trigeminal ganglion neurons, via the effects of high voltage-activated Ca2+currents, Ca2+influx and intracellular Ca2+concentration, as well as the underlying mechanisms of which in small trigeminal ganglion neurons. This study will benefit the understanding and development of cannabinoids in clinical practice.

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Copyedited by Slone-Murphy J, Xue T, Pan AH, Wang J, Qiu Y, Li CH, Song LP, Zhao M

10.4103/1673-5374.131607

http://www.nrronline.org/

Accepted: 2014-03-21