Nociception-induced spatial and temporal plasticity of synaptic connection and function in the hippocampal formation of rats: a multi-electrode array recording
- Xiao-Yan Zhao†1,
- Ming-Gang Liu†1,
- Dong-Liang Yuan2,
- Yan Wang2,
- Ying He1,
- Dan-Dan Wang1,
- Xue-Feng Chen2,
- Fu-Kang Zhang1,
- Hua Li1,
- Xiao-Sheng He2, 3Email author and
- Jun Chen1, 2Email author
© Zhao et al; licensee BioMed Central Ltd. 2009
Received: 8 September 2009
Accepted: 22 September 2009
Published: 22 September 2009
Pain is known to be processed by a complex neural network (neuromatrix) in the brain. It is hypothesized that under pathological state, persistent or chronic pain can affect various higher brain functions through ascending pathways, leading to co-morbidities or mental disability of pain. However, so far the influences of pathological pain on the higher brain functions are less clear and this may hinder the advances in pain therapy. In the current study, we studied spatiotemporal plasticity of synaptic connection and function in the hippocampal formation (HF) in response to persistent nociception.
On the hippocampal slices of rats which had suffered from persistent nociception for 2 h by receiving subcutaneous bee venom (BV) or formalin injection into one hand paw, multisite recordings were performed by an 8 × 8 multi-electrode array probe. The waveform of the field excitatory postsynaptic potential (fEPSP), induced by perforant path electrical stimulation and pharmacologically identified as being activity-dependent and mediated by ionotropic glutamate receptors, was consistently positive-going in the dentate gyrus (DG), while that in the CA1 was negative-going in shape in naïve and saline control groups. For the spatial characteristics of synaptic plasticity, BV- or formalin-induced persistent pain significantly increased the number of detectable fEPSP in both DG and CA1 area, implicating enlargement of the synaptic connection size by the injury or acute inflammation. Moreover, the input-output function of synaptic efficacy was shown to be distinctly enhanced by the injury with the stimulus-response curve being moved leftward compared to the control. For the temporal plasticity, long-term potentiation produced by theta burst stimulation (TBS) conditioning was also remarkably enhanced by pain. Moreover, it is strikingly noted that the shape of fEPSP waveform was drastically deformed or split by a TBS conditioning under the condition of persistent nociception, while that in naïve or saline control state was not affected. All these changes in synaptic connection and function, confirmed by the 2-dimentional current source density imaging, were found to be highly correlated with peripheral persistent nociception since pre-blockade of nociceptive impulses could eliminate all of them. Finally, the initial pharmacological investigation showed that AMPA/KA glutamate receptors might play more important roles in mediation of pain-associated spatiotemporal plasticity than NMDA receptors.
Peripheral persistent nociception produces great impact upon the higher brain structures that lead to not only temporal plasticity, but also spatial plasticity of synaptic connection and function in the HF. The spatial plasticity of synaptic activities is more complex than the temporal plasticity, comprising of enlargement of synaptic connection size at network level, deformed fEPSP at local circuit level and, increased synaptic efficacy at cellular level. In addition, the multi-synaptic model established in the present investigation may open a new avenue for future studies of pain-related brain dysfunctions at the higher level of the neuromatrix.
It has been gradually known that pain is a complex experience consisting of sensory-discriminative, affective-motivational, and cognitive-evaluative dimensions [1, 2]. Furthermore, there is now a consensus of idea that noxious information is processed by a distributed and interconnected neural network, referred to as neuromatrix, in the brain [3–6]. Unlike physiological state, pathological pain, when becomes persistent or chronic, can affect various higher brain functions (such as perception, emotion, cognition, and memory) through ascending pain pathways, leading to consequences of cognitive decline and mental disability. In the past three decades, the most advanced understanding about pain is that pathogenesis or chronicity of pain is attributable to sensitization of primary sensory neurons and synaptic plasticity in dorsal horn of the spinal cord [7–9]. To date, the mechanisms by which inflammatory or neuropathic pain is processed at the lower level of the pain pathway have been well characterized [7–11]. However, in clinic, chronic pain often results in not only sensory dysfunction (spontaneous pain, hyperalgesia and allodynia, etc.) but also emotional and cognitive disorders such as anxiety, amnesia and depression [12–14]. Unfortunately, so far, the influences of pathological pain on the higher brain functions are not clear and this may hinder the advances in clinical pain therapy. Therefore, unraveling how pain affects the emotion- or cognition-controlling regions at a higher level of the "pain matrix" would definitely improve our understanding of the process of pain chronicity and provide novel strategies for treating negative emotional symptoms of chronic pain in the clinical setting [4, 6].
There is substantial evidence indicating that the hippocampal formation (HF), an integral component of the limbic system [15, 16], is involved in pain processing besides its well documented roles in learning and memory formation [17–19]. Melzack and Casey (1968) proposed that the limbic forebrain structures, including the HF, play important roles in the 'aversive drive and affect that comprise the motivational dimension of pain' . Anatomically, the HF is positioned as a key interconnecting structure in Papez's circuit of the limbic system, mediating a variety of biological functions, including learning and memory, anxiety, emotion and sensorimotor integration [15, 21, 22]. More recent evidence using the atlas registration-based event-related (ARBER) analysis technique and whole-brain functional magnetic resonance (fMRI) imaging or 18F-fluorodeoxyglucose positron emission tomography (PET) clearly shows that dorsal, but not ventral, part of the rat HF was activated by subcutaneous formalin injection [23, 24]. Previous studies using electrophysiological [25–31] and neurochemical/biochemical [32–37] assays have demonstrated that the neuronal activities (pyramidal or interneuronal) and protein expression/activation within the HF could be altered by pain and stress. Moreover, intra-hippocampal microinjection of lidocaine , or antagonists acting at N-methyl-D-aspartic acid (NMDA) receptor [39, 40], 5-HT2A/2C receptor  and platelet-activating factor receptor  could result in an analgesic effect in the formalin test. Clinical observations show that electrical stimulation of the HF evokes painful sensations in humans [43, 44] and hippocampal lesion can partially alleviate chronic pain [45, 46]. Taken together, the above previous reports provide convergent evidence for the critical involvement of HF in pain processing and support the possibility that there might be some kinds of synaptic plasticity occurred in the HF characterized by functional changes in synaptic transmission and modulation as well as structural changes in synaptic connection under the condition of peripheral persistent nociception.
With regard to the impact of pain upon the brain, it has been revealed that chronic pain states can change the structure and morphology of the brain, namely central structural plasticity, which probably results in long-term dysfunction of synaptic transmission and modulation at different levels of the central nervous system (CNS) . In addition, long-term potentiation (LTP), a form of functional neuroplasticity, was also found to be associated with pain processing in recent years, except for its wide use as a unique synaptic model for learning and memory [48–50]. Actually, there have been a number of previous studies investigating LTP phenomenon in multiple pain-related CNS regions, including the spinal cord dorsal horn [51–53], primary somatosensory cortex (S1 area) [54, 55], amygdala [55, 56], anterior cingulate cortex [55, 57–61] and so on. As regards the HF, an enhanced LTP by pain was also reported in one previous study . In that study, it was found that LTP in the CA1 area could be facilitated by tail tip amputation-induced injury in mice and the increased synaptic efficacy was accompanied by a strong up-regulation of the immediate early gene product Egr1 . Because CA1 receives inputs from Schaffer collaterals of CA3 pyramidal cells which are innervated by entorhinal-dentate gyrus (DG) output [15, 16, 22], it is of particular importance to see whether there are parallel changes in synaptic connection and function in the DG area in response to persistent nociception. Furthermore, based upon the studies from Khanna's group, the neuronal activities in CA1 differ from each other in response to formalin-induced nociception, namely at the time when a discrete population of putative pyramidal cells are selectively activated, a large number of CA1 cells are suppressed in a widespread and prolonged manner, implicating a 'signal-to-noise' processing of pain in the CA1 area [27–31]. However, the interrelationship between different populations of CA1 neurons or between DG and CA1 regions are still not clear and requires to be further studied by multisite recording approaches.
The planar multi-electrode array (pMEA) is a unique and well-established tool for investigating, at a macroscopic level, the electrophysiological properties of living brain slices containing intact networks of neurons, providing a bridge between single cell testing and behavioral studies . Compared to traditional electrophysiology, the pMEA technique allows one to detect the activity of neuronal networks in both space and time [63–65], to record multiple sites simultaneously , and to make stimulating the recorded cells possible . To visualize the spatial and temporal information of pMEA recording, two-dimensional current source density (2D-CSD) imaging can also be used [68, 69]. Therefore, in the present study, using pMEA (i.e., Panasonic's MED64 system, see [68–70]) recordings combined with 2D-CSD imaging on acute hippocampal slices, we examined potential effects of peripheral persistent nociception on spatial and temporal plasticity of synaptic connection and function in the HF. The animal pain models we used are the bee venom (BV) test and the formalin test, both of them being well-developed animal models of persistent, inflammatory pain [71–76]. The results showed robust changes in both spatial and temporal plasticity of synaptic connection and function following peripheral persistent nociception.
Two types of field potentials were recorded in the HF
Pharmacological identification of two kinds of field potentials
Persistent pain produced spatial plasticity of synaptic connection and transmission in the HF
When examining the effects of BV-induced persistent pain on this kind of spatial plasticity, the mean total number of effective fEPSP was robustly increased in hippocampal slices prepared from rats receiving intraplantar injection of BV when compared to those from naïve or saline-treated animals at each stimulus applied. No appreciable difference was detected between saline control and naïve group (Fig. 6A). Within each group, the number rose gradually with increasing stimulus intensity and reached a stable level at around 90-120 μA. Locally pre-administration of an anesthetic agent (0.25% bupivacaine, 10 min prior to BV injection) resulted in an almost complete blockade of BV-induced increase in the number of fEPSP at a certain stimulation intensity (40-60% of the maximal response, 33.21 ± 1.25 vs. 27.00 ± 0.95 for BV-inflamed vs. BV-inflamed + block, n = 8 and 5, P < 0.05, Fig. 6B).
Almost similar results were obtained in the formalin test. As shown in Fig. 7B, compared with the saline control group, subcutaneous injection of 5% formalin solution elicited a larger synaptic connection size over the HF, reflected as the significantly increased number of effective fEPSP at the stimulation intensity of 120 μA, 180 μA and 199 μA.
Persistent pain enhanced temporal plasticity of synaptic responses in the HF
Induction probability of LTP is also a parameter describing functional stability of facilitated synaptic efficacy that may reflect the network state of the CNS structures. Following recording of a stable baseline, LTP was successfully elicited in 16 out of 23 naïve slices, with an induction rate of 69.6%. The success rate of LTP induction was about 72.4% in the saline-treated group (21/29), which was not significantly different from the naïve control. Nevertheless, the rate was increased to 85.7% (24/28) and 83.3% (10/12) in the BV- and formalin-treated group of slices.
The waveform of the fEPSP is determined by field current direction and distribution across the synaptic interconnections due to depolarization and repolarization of the membrane. The 2D-CSD imaging is based mostly upon the spatiotemporal distribution of current sources (positive-going waveforms) and sinks (negative-going waveforms). Thus, the changes in waveforms of fEPSP will lead to changes in current sources and sinks, resulting in corresponding changes in 2D-CSD imaging. In the current study, it was surprisingly noted that, in some cases (about 50% of all the slices exhibiting LTP from BV- or formalin-inflamed rat), the shape of both positive-going and negative-going fEPSP was deformed or tortured at around 30-60 min after TBS conditioning on the hippocampal slices of rats which had suffered from persistent nociception, namely from the original single phase to double or multiple phases (Fig. 2C and Fig. 11A). These alterations in the appearance or structure of fEPSP were also reflected in the 2D-CSD plots (Fig. 3). After application of TBS onto the PP pathway, instantaneous 2D-CSD plots computed across all 64 electrodes revealed a clear rise in the intensity of current signals detected from slices of the saline-treated group (Fig. 3A, lower row). In naïve slices, 2D-CSD images constructed before and after LTP induction were similar to those from the saline group (data not shown). Unlike naïve or saline-treated slices, plastic alterations in 2D-CSD images following BV-induced persistent pain seemed rather complex. While the pre-TBS profile was essentially the same as that described above (Fig. 3B, upper row), post-TBS pictures (Fig. 3B, lower row) revealed a dramatic and interesting change in the spatial distribution of current sinks and sources, from single dipole to binomial events. Specifically, the initial fiber volley was followed by the growth of a current source in the DG region, accompanied by a current sink in the CA1 area (see image at 5 ms). The sinks and sources then increased in density, extended in scope, and reached a peak at 7 ms. However, by 9 ms, currents on both the DG and CA1 became a mixture of sources and sinks. This state persisted for the next 10 ms before vanishing around 20 ms. Moreover, tetanization of the PP pathway produced a more robust increase in the intensity of CSD signals, with the disparity between post-TBS and pre-TBS being much larger in the BV-treated group than the others (Fig. 3).
Roles of NMDA and AMPA/KA receptors in mediation of persistent nociception-induced spatial and temporal plasticity in the HF
When it comes to the temporal plasticity, the maintenance of LTP was lightly but significantly blocked by AP5 (100 μM), with the inhibition rate being 7.42 ± 1.83%, 6.87 ± 2.38% and 17.21 ± 2.80% for the DG fEPSP of naïve, saline- and BV-treated group, respectively. A similar pattern of suppression was found in the case of CA1 fEPSP, with the suppression rate being 8.51 ± 1.41%, 3.48 ± 1.01% and 18.84 ± 2.03%, respectively. Bath application of CNQX (10 μM) dramatically blocked the maintenance of LTP evoked in three groups of slices. Curiously, there was no marked difference in the inhibition rate of CNQX among each group for both types of fEPSP (data not shown).
Advantages of multisite electrophysiological recording using pMEA
Electrophysiological recordings with traditional microelectrodes have provided fruitful information concerning membrane properties and local neural circuitry at the single channel, single synapse and single neuron levels. However, some of the most serious limitations of the conventional glass micropipette techniques, such as limited recording site and time, typically preclude any chance of testing hypothesis regarding neural interactions as spatially extended circuits over a longer period. Substrate-integrated pMEA offers an alternative to classical electrophysiology for recording the electrical activity of cells and tissues of neuronal or cardiac origin . The advantages of pMEA lies in that: (1) enable gathering large amounts of spatial information on the internal dynamics of networks with multisite recordings [65, 78]; (2) long-term analysis of the spatiotemporal distribution of network level electrical activity [63, 64, 66]; (3) stimulating and recording the electrophysiological activity of many sites within a slice [63, 65]; (4) steady recording that are less sensitive to factors such as mechanical vibrations [65, 78]. Overall, the pMEA technology represents a valuable tool for stably recording electrophysiological data from multiple sites over extended periods of time from a variety of biological preparations, facilitating our understanding of complex brain operations and functions in normal and pathological states [64, 68–70, 79, 80].
Distinct forms of fEPSP exist between DG and CA1 area
In the present study, electrical stimulation of the PP fibers typically evoked two forms of fEPSP in rat hippocampal slices. The positive-going fEPSP was mainly distributed within the DG area, while the negative-going waveforms were largely localized in the area across stratum lacunosum-moleculare of CA1 region where apical dendrites of pyramidal cells locate [15, 16, 22]. This phenomenon was further validated by 2D-CSD analysis. Generally, a current source always surfaced in the DG, whereas a sink signal consistently formed in the CA1 for most of the sampling period (Fig. 3). It is well known that the PP may include two sources of origins: one belongs to polysynaptic intrahippocampal pathway originating from layer II of entorhinal area and projecting to the stratum moleculare of the DG, while the other belongs to direct intrahippocampal pathway originating from layer III of entorhinal area and targeting to the apical dendrites of the CA1 pyramidal cells [15, 16, 22, 81–83]. Thus this result suggests that stimulation of the PP fibers could simultaneously activate multisite synaptic contacts in both DG and CA1 regions. The CA1 synaptic responses are not likely to be mediated by synaptic transmission through the DG-CA3-CA1 inter-relay, because the peak latencies of both positive-going and negative-going fEPSP were not significantly different. Therefore, it could be reasonably assumed that the positive-going fEPSP might be due to engagement of the synaptic connection between entorhinal projection and DG granular dendrites, while the negative-going fEPSP might result from direct activation of the entorhinal-CA1 pathway.
Although it has been believed that both kinds of PP fibers are glutamatergic, the glutamate receptor composition in the DG and CA1 is likely to be different according to our present pharmacological results. As shown in Fig. 5, both the DG positive-going and the CA1 negative-going fEPSP were completely blocked by CNQX, however, the latter were less sensitive to AP5 than the former, suggesting a possible difference in localization density of glutamate receptor subtypes between these two regions. This finding will be of particular interest and help to further identification of the properties of two kinds of PP fibers and their distinct targets in different subregions of the HF.
Spatial plasticity of synaptic connection and transmission in the HF caused by persistent nociception
Mechanisms underlying spatial plasticity of synaptic connection and transmission may operate in two ways. One is simply a recruitment of presynaptic input onto a single cell, leading to gain of the fEPSP at the previously activated synaptic contacts . The other possibility is an increase in the number of synaptic contacts onto more newly activated cells or an increase in postsynaptic dendritic spines on the previously activated cells, leading to enlargement of the effective network size. In the current study, we successfully recorded both types of spatial plasticity. As illustrated in Fig. 8 and 9, BV- or formalin-induced persistent nociception moved the I-O functional curves leftward, although not in a parallel manner, to those of the naïve and saline control rats. This represents an increase in synaptic efficacy due to recruitment of more inputs or activation of post-synaptic molecular and cellular events . In addition, we found a new type of spatial plasticity with a distinct enlargement of neural network size probably due to increase in the number of synaptic contacts onto more newly activated cells or increase in post-synaptic dendritic spines on the previously activated cells caused by peripheral persistent nociception (Fig. 6 and 7). Taken together, these findings strongly reinforce the notion that peripheral persistent pain stimulation can really result in spatial plasticity of synaptic activity in the HF, revealed as enhanced responsiveness to electric stimuli as well as enlargement of the scope where effective fEPSP could be elicited. These spatial characteristics of synaptic plasticity, revealed by our MED64 recording system, are far beyond the scope of other classical electrophysiological recording techniques (such as the in vivo electrophysiology and in vitro patch clamp recording) and further highlight the superiority of multisite recording.
The present report also provided the first attempt to explore potential pharmacological mechanisms leading to this sort of spatial plasticity. It is of particular importance to point out that BV-evoked spatial summation of multisite synaptic responses is not due to tetanic stimulation applied to the PP fibers, nor is there any involvement of NMDA receptors in the process. Our pharmacological study showed a complete reversal of the enlarged synaptic connection by CNQX (Fig. 12), implicating a crucial role of AMPA/KA receptors in mediating nociception-induced spatial plasticity. Since the mechanisms underlying learning and memory in the HF are highly dependent on activation of NMDA receptors , the mechanisms for nociception-induced spatial plasticity of synaptic connection in the HF are likely to be different. However, precise mechanisms for persistent nociception-induced enlargement of synaptic connection network still remain unclear and require to be further studied.
With respect to the input pathways by which peripheral nociceptive information can be conveyed to the HF, at least two major sources are considered. One is septal-hippocampal cholinergic projection pathway which originates from medial septal nucleus and nucleus of the vertical limb of the diagonal band of Broca and passes through fornix back to both the DG granular cells and the CA1 pyramidal cells . The other one is entorhinal-PP pathway per se which mainly receives projections from posterior parietal association cortex and anterior cingulate cortex to the entorhinal area . It is known that the two cortical regions receive nociceptive information from primary somatosensory cortex which is the target of spinothalamic tract [1–3, 20]. Recently, we found that BV-induced persistent pain produced long-lasting activation of mitogen-activated protein kinase subfamily members in both S1 area and HF [37, 85]. Up-regulation of c-Fos protein was also predominantly localized within layer II-III of the S1 region in response to intraplantar BV injection . Taken together, the spatial plasticity of synaptic connection and organization might be caused by persistent nociceptive drive produced by long-lasting activation and sensitization of primary nociceptors and spinal dorsal horn nociceptive neurons [72, 73]. This hypothesis is strongly supported by the elimination of enlarged synaptic connection size (increase in number of fEPSP) in the HF by pre-blockade of nociceptive impulses in the present study (Fig. 6). In addition, the spatial plasticity may also be caused by disinhibition of inhibitory γ-aminobutyric acid (GABA) or other endogenous neuropeptides such as enkephalin, substance P, vasoactive intestinal polypeptide, cholecystokinin and somatostatin in the HF . Although some reports indicate the involvement of endogenous opioid and GABAA receptors in nociceptive processing within the HF , the mechanisms underlying this hypothesis are still poorly studied and need to be further investigated using this model.
Temporal synaptic plasticity in the HF caused by persistent nociception
Mammalian hippocampal LTP is a widely studied model of activity-dependent changes in synaptic efficacy that is assumed to provide the physiological basis for learning and memory [48–50]. A long-lasting, NMDA receptor-dependent LTP has been repeatedly elicited in the excitatory synapses made by PP fibers onto granular cells of the DG [88, 89]. A few of studies have also examined the pharmacology and plasticity of the entorhinal-CA1 pathway [90, 91]. In spite of these results, very limited information is available concerning LTP induction and persistence in these two pathways at the network level. In the present study, using a unique multi-electrode array recording technique, LTP of sufficient magnitude and duration could be reliably and simultaneously recorded in both pathways following TBS conditioning of the PP fibres (Fig. 1 and 2). Future experiments will be directed towards dissecting the molecular and cellular changes underlying these forms of network LTP.
A notable finding of this study was that BV- or formalin-induced inflammatory painful stimulation increased the LTP induction probability and magnitude in both DG and CA1. The enhanced LTP could be completely abolished by blocking the nociceptive inputs from the peripheral injury site (Fig. 10), suggesting a strong correlation with existence of pain. These observations are compatible with the conclusion that BV- or formalin-induced persistent pain could also produce temporal plasticity of synaptic activity in the HF, reflected as increased probability of LTP induction and augmented LTP magnitude.
The most striking feature of nociception-produced synaptic plasticity in the HF was a change in the appearance or shape of fEPSP. In almost half of the recorded slices from the BV- and formalin-inflamed group, the structure of the fEPSP waveform was remarkably deformed or tortured by persistent nociception in that it became bi- or multi-phasic at about 30-60 min after TBS conditioning, whereas the waveform of fEPSP was normally shown to be mainly single phase (Fig. 2 and 11). This was further demonstrated by the 2D-CSD plots, showing a conversion from single current source-sink dipole to binomial events after TBS in the BV-inflamed group (Fig. 3). The mechanisms underlying the deformation of fEPSPs by persistent nociception are not clear, however, the roles of septal-hippocampal cholinergic regulation of the HF should be considered, because the LTP conditioning parameter used here was TBS that mimicked the septal-hippocampal cholinergic stimulation.
Differences in the spatial and temporal plasticity produced by formalin and BV-evoked inflammatory pain
One important point revealed by these data is the possible difference in the degree or extent of spatial and temporal plasticity elicited by BV- and formalin-induced persistent pain. As can be evidently seen from the present results, there are indeed some differences existing between these two models. For the spatial plasticity, although both models of inflammatory pain could result in a significant leftward shift of the I-O functional curves of the fEPSP amplitude or slope, the trend was rather less marked in the case of formalin-evoked persistent pain (Fig. 8 and 9). Intriguingly, no appreciable difference was found in the number of fEPSP between formalin- and BV-treated group (Fig. 6 and 7). For the temporal plasticity, formalin-induced LTP enhancement was still much smaller than that by BV injection (Fig. 10 and 11). This partial discrepancy of spatiotemporal plasticity produced by the two models of pain are in good accordance with previously reported inter-model differences in both behavioral and electrophysiological assays [72–76, 92–94].
In previous studies conducted in the formalin test, it was found that most of the CA1 pyramidal cell activities were suppressed by formalin injection, however, the theta rhythmic activities were increased in the typical manner of formalin-elicited biphasic behavioral and neuronal responses [26–31]. Moreover, the expression of neurokinin 1 receptors and brain-derived neurotrophin factors in the hippocampus was also suppressed by subcutaneous injection of formalin [35, 36]. The above two groups' results are in contrast to what we observed in the present study. The discrepancies are presumably ascribed to the differences in subtle experimental variables (e.g. the concentration, volume and site of formalin injection, measuring methods, observation targets and so on) but may also reflect the complexity of the higher brain structure in dealing with pain. That is, even the same kind of painful stimulus could lead to a myriad of complicated even contrasting changes in hippocampal morphology, molecular biology and physiology. Nonetheless, novel information about modulation of sensitivity, plasticity, and function of the hippocampus by painful stimuli and the gaining knowledge of the underlying mechanisms may shed new light on the roles of this limbic region in pain processing and lead to discovery of new therapeutic targets and strategies for treating not only pain but also co-morbidities of pain in the clinical setting.
In summary, a recently-developed multi-electrode array technique was successfully applied to acutely dissociated hippocampal slices in this study to demonstrate that peripheral persistent nociception could produce both spatial and temporal plasticity of synaptic connection and function in the HF. The spatial plasticity of synaptic activities is more complex than the temporal plasticity, comprising of enlargement of synaptic connection size at network level, deformed fEPSPs at local circuit level and, increased synaptic efficacy at cellular level. Finally, the multi-synaptic model established in the present study might be useful for further elucidating brain processing of emotional and cognitive aspects of pain, as well as screening novel analgesics for treating brain disorders associated with chronic pain.
Experiments were carried out on male albino Sprague-Dawley rats provided by Laboratory Animal Facilities of both Capital Medical University (CCMU) and the Fourth Military Medical University (FMMU). All animals were with ages of 4 weeks old (weighing 120-160 g) and were housed in groups of five per cage under controlled laboratory conditions (12 h light/12 h dark, temperature 22-26°C, air humidity 55-60%). They had free access to commercial rat pellets and tap water. The experimental procedures were approved by the Institutional Animal Care and Use Committee at both CCMU and FMMU. All animals were maintained and cared for in compliance with the guidelines set forth by the International Association for the Study of Pain . The number of animals used and their suffering were greatly minimized. The experiments were blinded; all experimental rats were randomly divided into five groups: (1) naïve rats without treatment; (2) rats with subcutaneous injection of 0.9% sterile, isotonic saline solution; (3) rats with subcutaneous injection of whole BV solution; (4) rats with subcutaneous injection of formalin; and (5) rats with subcutaneous injection of 0.6 ml bupivacaine (0.25%) into the hind paw 10 min prior to ipsilateral BV treatment.
Induction of persistent pain
Persistent pain was induced with the BV test as described previously . The BV used in this study was lyophilized whole venom from Apis mellifera (Sigma, St. Louis, MO) dissolved in 0.9% sterile saline. A volume of 50 μl saline containing 0.2 mg BV was used during the whole experiment, because previous studies have shown that 4 μg/μl was the optimal dose to produce a prolonged pain-related behavioral response . With respect to the formalin text, for each injection, 0.05 ml of 5% formalin (37.5-40% formaldehyde solution diluted in 0.9% sterile saline) was used in the present study [74, 92, 94]. The whole BV or diluted formalin solution was administered by subcutaneous injection into the posterior plantar surface of the left hind paw of rats . The animals were carefully handled during the process to reduce the possible interruption of results caused by handling-induced stress. Intraplantar injection of the same volume of physiological saline served as the control group.
Preparation of multi-electrode array
Procedures for the preparation of the Multi-Electrode Dish (Panasonic, MED probe) were almost the same as described by . The device had an array of 64 planar microelectrodes, each 50 × 50 μm in size, arranged in an 8 × 8 pattern (inter-electrode distance, 300 μm). The microelectrode's large size resulted in lower impedance, enabling both reliable stimulation and a higher signal to noise ratio when recording. Before use, the surface of the MED64 probe was treated with 0.1% polyethyleneimine (Sigma, St. Louis, MO; P-3143) in 25 mM borate buffer (pH 8.4) overnight at room temperature. This coating helped establish sufficient adhesion of the slice to the probe surface, resulting in enough perfusion by the recording buffer (2-3 ml/min) to keep the slice healthy for more than 6 h of fEPSP recording . The probe surface was rinsed three to five times with sterile distilled water before immediate use. In general, the MED64 probes could be re-used for approximately 30-40 recording sessions with a mean duration of 4-6 h. Electrode properties could be maintained constant by carefully cleaning the probe with deionized water following each recording session.
Preparation of acute hippocampal slices
The general procedures for preparing acute hippocampal slices were similar to those described previously [68–70]. Male Sprague-Dawley rats aged 25-30 days were sacrificed by decapitation after anesthesia with 4% sodium pentobarbital (0.1 ml/100 g, i.p.) 2 h after subcutaneous saline or BV or formalin injection. Subsequently, the whole brain was rapidly removed and immediately soaked in ice-cold, oxygenated preparation buffer of artificial cerebrospinal fluid (ACSF) for approximately 1-2 min. The ACSF contained 124 mM NaCl, 3.3 mM KCl, 1.2 mM KH2PO4, 2.4 mM MgSO4, 10 mM glucose, 26 mM NaHCO3, 2.5 mM CaCl2, and had a pH of 7.4 adjusted by gassing with 5% CO2/95% O2. Appropriate portions of the brain were then trimmed and the remaining brain block was placed on the ice-cold stage of a vibrating tissue slicer (Dosaka, DTK-1000). Here, it deserves mentioning that all the present experiments were performed on the right (i.e. contralateral to the BV injection side) anterior hippocampus of rats in three groups, ranging from Bregma -2.52 mm to Bregma -4.08 mm according to the Atlas of the Rat Brain . The stage was immediately filled with oxygenated and frozen ACSF. The thickness of each tissue slice was set at 350-400 μm. Each slice was gently taken off the blade by a writing brush, trimmed, and immediately soaked in an incubation chamber containing the oxygenated ACSF for 2 h at room temperature.
After incubation, one slice was selected and positioned on the MED64 probe in such a way that the whole HF was entirely covered by the 8 × 8 array. Once the slice settled, a netting ballast (U-shaped platinum wire with regularly spaced hair pieces) was carefully disposed on the slice to immobilize it. For the electrophysiological recordings, the probes with immobilized slices were connected to the stimulation/recording component of MED64. The slice was continuously perfused with oxygenated, fresh ACSF at the rate of 2-3 ml/min with the aid of a peristaltic pump (PERI-STAR™, WPI, USA). After a 20 min recovery of the slice, one of the 64 available planar microelectrodes was selected from the 64-switch box for stimulation following visual observation through a charge-coupled device camera connected to an inverted microscope. When not specified, monopolar, biphasic constant current pulses (30-199 μA, 0.1 ms duration) generated by the data acquisition software were applied to the PP at 0.1 Hz. Field potentials evoked at the remaining sites were amplified by the 64-channel main amplifier and then digitized at a 20 kHz sampling rate. The digitized data were displayed on the monitor screen and stored on the hard disk of a microcomputer. Five successive responses were averaged automatically in real time by the recording system. The viability of the slices was kept constant across different sets of recording sessions by measuring the threshold for evoking fEPSP of adequate amplitude.
After selecting the best stimulation site and stabilizing the synaptic responses for about 30 min, an I-O curve was first determined for each group using the measurements of fEPSP amplitude or slope in response to a series of stimulation intensities from 30 μA to 199 μA (30 μA, 60 μA, 90 μA, 120 μA, 150 μA, 180 μA, 199 μA). Because of the technical limits of the stimulus generator, higher intensities (>199 μA) could not be applied and were not tested in the present study. The intensity of the test stimulus was then adjusted to elicit 40-60% of the maximum based on the I/O curves. Next, the stability of the whole recording system was checked by recording baseline responses for another 30 min (3 × 10 min). For LTP induction, the TBS protocol was used, which consisted of 10 bursts, each containing 4 pulses at 100 Hz with an inter-burst interval of 200 ms. It is widely accepted that such a protocol resembles in vivo conditions and has been suggested as a method to establish a link between artificial and natural synaptic activity . In addition, LTP induced by such stimulation appears to be more robust and stable than that induced by other means . To standardize tetanization strength in different experiments, the TBS strength was set at an intensity evoking almost half of the maximal magnitude of fEPSP. After TBS, the test stimulus was repeatedly delivered (at the identical intensity as baseline) once every 10 min for more than 2 h to allow for the observation of any changes in LTP magnitude and duration.
In experiments regarding pharmacological characterization of fEPSP, the stability was first determined by recording the baseline responses for about 30 min as described above. Then, TTX (0.5 μM and 1 μM), AP5 (50 μM and 100 μM) and CNQX (10 μM) were bath applied to separate slices at a rate of 2 ml/min. For the high magnesium-low calcium solution, the concentration of CaCl2 was lowered to 0.25 mM and the concentration of MgSO4 was raised to 4.0 mM in the ACSF. In another set of experiments, either AP5 (100 μM) or CNQX (10 μM) was bath applied at 2 h after LTP induction (a sustained peak level reached at this time) to observe their actions on spatial and temporal plasticity in the HF. In any of the above cases, complete solution exchange was achieved within 10 min of drug infusion or ionic substitution. Subsequently, fresh ACSF washed in until the drug effects vanished and the normal synaptic responses essentially recovered.
Current source density analysis
With the normalized CSD values at the center of the electrodes, it became possible to compute the density at any point (x, y) within the 8 × 8 array using bilinear interpolation. After all of the above calculations, we used the color yellow to represent positive currents (sources), the color blue to represent negative currents (sinks), and the color black to map zero current. Finally, CSD images at selected time points were plotted across all 64 recording sites for each group of slices.
All drugs were purchased from Sigma-Aldrich and, except for CNQX, were dissolved in deionized water as stock solutions for frozen aliquots. They were diluted to the desired concentration in ACSF before immediate use. CNQX was dissolved in dimethylsulfoxide (DMSO, final concentration 0.1%) and prepared as described above.
For quantification of the I-O relationship, the amplitude and slope of fEPSP were analyzed off line by the MED64 Conductor. For LTP data, the amplitude and slope of evoked fEPSP were normalized and expressed as a percentage of the averaged value measured during the last 10 min baseline period. Evaluations of drug effects were carried out on the basis of the difference between the pre-drug recording and the 10 min after drug infusion (when the drug effect was most potent). The total number of effective fEPSP (> 20% baseline) reliably recorded over the HF was counted by an experimenter unaware of the experimental design and averaged across slices for each group. Data sets included results from only one slice per rat (n = number of slices). All data were presented as mean ± S.E.M. When necessary, the statistical significance was determined using either the Student's t test (paired and two-independent sample) or one-way ANOVA (post-hoc Fisher's PLSD). The level of P < 0.05 was assumed as statistically significant.
This work was supported by the National Basic Research (973) Program of China 2006CB500800, National Innovation Team Program of Ministry of Education IRT0560, National Natural Science Foundation of China grants (30670692 and 30770668) to JC and Military Health Foundation to JC (06G095) and X-SH (06MA212). The authors thank C-Y Gao, L-F Zhao and Y-Y An for their help in technical training.
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