Corrigendum: Deactivation of excitatory neurons in the prelimbic cortex via Cdk5 promotes pain sensation and anxiety

Nature Communications 6: Article number: 7660 (2015); Published: 16 July 2015; Updated: 10 October 2016 In Fig. 7i of this Article, a different section of the control trace was used to represent the Cdk5 shRNA trace. The correct version of Fig. 7, including a new representative Cdk5 shRNA trace in panel i, appears below as Fig.

A ccording to epidemiological data of Europe, one-fifth of the world population suffers from chronic pain 1 . During acute pain, physiological and psychological processes, such as perception, cognition, emotion, motivation and memory, adapt to prevent further damage. However, for chronic pain, such changes are maladaptive; thus, chronic pain is typically accompanied by comorbidities, such as hemi-inattention, deficits in cognition and memory, mood disorders and decreased motivation 2 . Clinically, patients with chronic pain are at a heightened risk for developing anxiety 3,4 . Likewise, patients with anxiety express more pain complaints and typically exhibit greater perceptual and cognitive impairments 5 . The interactions between pain and anxiety have made the evaluation and treatment of chronic pain clinically challenging. Moreover, the specific neural circuits involved in chronic pain-induced anxiety are not yet fully understood.
In chronic pain, nociceptors trigger an increased rate of action potentials (APs) and subsequently convey pain signals to several brain areas that are thought to be involved in the initiation of pain perception and anxiety 6 . Functional imaging studies suggest the involvement of primary somatosensory cortex (S1) and secondary somatosensory cortex (S2) in processing the sensorydiscriminative component of pain and the anterior cingulate cortex (ACC) and prefrontal cortex (PFC) in processing the affective-motivational component of pain 7 . Previous studies largely focus on the role of the ACC in affective responses to pain. Long-term potentiation (LTP) in the ACC is thought to maintain chronic pain, and the disruption of LTP in the ACC alleviates chronic pain 8 . Chronic pain and anxiety are both associated with the occlusion of a presynaptic form of LTP in the ACC, suggesting that the two forms of LTP in the ACC may mediate the interaction between anxiety and chronic pain 9 .
In addition to the ACC, recent studies address the importance of the medial PFC (mPFC) in various cognitive and emotional processes, and pain-related perceptions 10 . Functional and morphological abnormalities in the mPFC are present in a chronic pain animal model 11 . Moreover, the mPFC exhibits increased blood flow following an acute nociceptive stimulation 12 . Both background and evoked activity of mPFC neurons is decreased in an arthritis chronic pain model 13,14 and it has been speculated that the progression of pain from acute to chronic is accompanied by a decrease in mPFC activity 15 . In addition to its role in pain sensation, the mPFC has also been implicated in anxiety. Functional imaging studies indicate that the mPFC is hypoactive in anxiety patients 16 . The mPFC is also involved in anxiety-like behaviours in animal models of stress 17,18 . Based on these evidence, we hypothesized that the mPFC is critical in the initiation of pain-related anxiety and the modulation of pain sensation.
In this study, we use a chronic inflammatory rodent pain model to examine the role of mPFC in chronic pain and anxiety. We show that chemically lesioning the PL, a sub-region of the mPFC, contralateral but not ipsilateral to the inflamed hind paw in rats attenuates anxiety-like behaviours and heat hyperalgesia, and that the intrinsic excitability of layer 2/3 excitatory neurons in the contralateral PL is decreased. When optogenetically activated, contralateral PL neurons exert analgesic and anxiolytic effects in chronic inflammatory pain mice; on the other hand, optogentically inhibiting them has an anxiogenic effect in naive mice. We subsequently show that the decreased activation of excitatory neurons in the contralateral PL of chronic pain rats is due to activation of cyclin-dependent kinase 5 (Cdk5), and that knockdown of Cdk5 reverses the deactivation of these excitatory neurons and attenuates anxiety-like behaviours and heat hyperalgesia. Together, these findings provide new insights into emotional and pain treatment in clinical chronic pain management.

Results
Lesion of contralateral PL attenuates pain and anxiety. To address the role of the mPFC in the modulation of pain sensation and pain-induced anxiety, we used a complete Freund's adjuvant (CFA)-induced chronic inflammatory pain model. Rats exhibited persistent heat hyperalgesia in the ipsilateral hind paw compared with the contralateral hind paw at 1, 7 and 14 days after CFA was injected in the left hind paw (Fig. 1a). Chronic pain rats exhibited both decreased time in the open arms and decreased open-arm entries of the elevated plus maze (EPM) as well as decreased time in the centre of the open field test (OFT) both 1 and 7 days after CFA injection (Fig. 1b,d); in contrast, general locomotor ability was unaffected (Fig. 1c,e). These results suggest that CFA-induced pain symptoms and anxiety-like behaviours develop and rapidly reach a plateau, providing a well-defined model to study pain sensation and pain-related anxiety-like behaviours.
To pinpoint the specific sub-region(s) in the mPFC that are responsible for pain sensation and pain-induced anxiety, we bilaterally damaged the three sub-regions, the cingulate cortex area 1 (CG1), PL and infralimbic cortex (IL), respectively, by micro-infusion of quinolinic acid (QA), a potent neurotoxic compound. The injection of QA induced the neuronal loss suggested by the NeuN immunostaining ( Supplementary Fig. 1). Following bilateral lesion of the PL, rats exhibited increased paw withdrawal latencies (PWL), increased time in the open arms and centre and increased open-arm entries (Fig. 1f), whereas bilateral lesions of the CG1 or IL had no effect on the PWL, EPM or OFT performances (Fig. 1g,h). Bilateral lesion of the PL in naive rats attenuated anxiety-like behaviours in the EPM and OFT without affecting the PWL ( Supplementary Fig. 2). These findings suggest that the PL rather than the CG1 or IL may be responsible for the modulation of pain sensation and the initiation of anxiety-like behaviours induced by CFA. Considering pain signalling is conveyed to the contralateral cortex from the level of spinal cord, we next examined the consequences of individually damaging the contralateral and ipsilateral PL on the modulation of pain sensation and pain-related anxiety-like behaviours. In rats with contralateral PL damage, the PWL was augmented and the time in the open arms and open-arm entries in the EPM as well as the time in centre of the OFT increased (Fig. 2a). In contrast, ipsilateral lesion of the PL did not affect heat hyperalgesia or anxiety-like behaviours (Fig. 2b). It has been reported that painassociated affect is more pronounced when pain is localized in the left side of the body 19 . To exclude the possibility of cortical function lateralization, we damaged the right hind paw with a CFA injection and lesioned the left (contralateral) PL and obtained similar results as those observed following CFA injection in the left hind paw and right PL lesion (Fig. 2c,d). These results suggest that the contralateral but not ipsilateral PL has a vital role in the modulation of pain sensation and pain-related anxiety-like behaviours.
Contralateral PL excitatory neurons are deactivated post CFA. To address how the contralateral PL is involved in CFA-induced heat hyperalgesia and pain-related anxiety, we first tested whether chronic pain alters the physiology of PL neurons by recording spontaneous excitatory post-synaptic currents (sEPSCs) in layer 2/3 neurons in PL using whole-cell patch clamp recordings. Excitatory pyramidal neurons in naive rats exhibited spike frequency adaption in response to a depolarizing current pulse (Fig. 3a). At 1 day post CFA injection, excitatory layer 2/3 neurons in the contralateral PL exhibited increased sEPSC frequencies and amplitudes compared with those of naive rats (Fig. 3b-d). These results, which were also confirmed by differences in the cumulative probabilities of sEPSC frequency ARTICLE NATURE COMMUNICATIONS | DOI: 10.1038/ncomms8660 and amplitude (Fig. 3c,d), are consistent with previous work using a spared nerve injury chronic pain model 11 .
We subsequently determined whether CFA injections altered the intrinsic excitability of contralateral PL neurons by examining biophysical characteristics of APs. APs were evoked by superimposed positive current steps (Fig. 3e) from a baseline potential of À 65 mV. A rightward shift in the input-output curve appeared 1 day after CFA injection, and significant differences were observed from current injections ranging from 180 to 300 pA (Fig. 3f). Examination of input-output curves indicated that fewer APs were elicited by depolarizing current steps at 1 day following CFA, compared with recordings obtained from naive rats. These results are consistent with previous results obtained in an arthritis pain model 14 . The current required to drive spike firing at 8.75 Hz was substantially greater at 1 day following CFA compared with that required to drive spike firing in naive rats (Fig. 3g,h). To analyse this further, the firing threshold of the first AP at 8.75 Hz was determined by a phase plot (Fig. 3i).  The neurons taken from rats 1 day after CFA injection have a more depolarized firing threshold compared with the neurons in naive rats (Fig. 3j). Additionally, the resting membrane potential was slightly more positive in neurons taken from rats 1 day following CFA injection as compared with that observed in naive controls, whereas no significant difference in input resistance was identified between groups ( Supplementary Figs 3a,b). These results suggest that although glutamatergic synaptic transmission in the contralateral PL is enhanced, the intrinsic excitability of excitatory neurons is decreased at the single-neuron level 1 day following CFA injection.
Activation of PL excitatory neurons reduces pain and anxiety.
To determine whether the deactivation of excitatory neurons in the contralateral PL is required for pain-induced behavioural impairments, we used optogenetics techniques that enable activation or inhibition of cell-type-specific neurons. Since the optogenetic experiments were performed in C57BL/6 mice, we first confirmed that CFA also induced anxiety-like behaviours in C57BL/6 mice in EPM and OFT ( Supplementary Fig. 4). To enable optical excitation of PL excitatory neurons, we infected PL excitatory neurons using an adeno-associated viral vector serotype 5 (AAV5) carrying channelrhodopsin-2 (ChR2) under control of the CaMKIIa promoter (Fig. 4b). We used multichannel recordings to determine effective illumination parameters. We found that 25-ms pulses of 473 nm blue light presented at 20 Hz with an intensity of 6-9 mW increased the firing rate of excitatory neurons from 1.59±0.42 to 13.49±1. 16 Hz in AAV5-CaMKIIa-ChR2-mCherry-infected CFA mice (Fig. 4c,d).

Confirmation of viral expression Handling
Virus injection and optic fibre implantation neurons, we compared behaviour of AAV5-CaMKIIa-ChR2-mCherry-infected mice with that of a control group of mice infected with a control virus (AAV5-CaMKIIa-mCherry) but receiving identical optical stimulation. Photostimulation of contralateral PL excitatory neurons increased the time spent in the open arms and open-arm entries of the EPM (Fig. 4f,g) and the time in the centre of the OFT (Fig. 4h,i). However, activation of the contralateral PL excitatory neurons also increased the travel distance in the OFT (Fig. 4i). We further tested whether the contralateral PL was involved in the modulation of pain sensation. The PWL was measured every 3 min (for a total of four repeats) under 20 Hz 473-nm blue light photostimulation, and the mean PWL was calculated. The activation of contralateral PL excitatory neurons significantly increased the PWL, which suggests an alleviation of heat hyperalgesia (Fig. 4e). As 1 day post CFA injection may not be considered chronic, we further tested a later time-point post CFA injection. Activation of contralateral PL excitatory neurons also exerted analgesic and anxiolytic effects 7 days after CFA injection ( Supplementary Fig. 5). However, the activation of the excitatory neurons in the ipsilateral PL, contralateral CG1 or IL did not affect anxiety-like behaviours or heat hyperalgesia (Supplementary Figs 6-8), confirming the specific role of the contralateral PL. Furthermore, activation of excitatory neurons in the ipsilateral PL also increased the distance travelled in the OFT ( Supplementary Fig. 5d), suggesting that the relief of anxiety-like behaviours via the activation of contralateral PL excitatory neurons is not a result of the increase in travel distance.
Previous studies indicate that the mPFC is involved in anxietylike behaviours 17,18 . To exclude the possibility that the mPFC regulates anxiety relief independent of pain state, we optogenetically activated PL excitatory neurons unilaterally in naive mice, and no obvious changes in anxiety-like behaviours were observed ( Supplementary Figs 9a-d), indicating that the relief of anxiety-like behaviours in the CFA mice was painrelated. However, the PWL was increased in naive mice after PL excitatory neuron activation ( Supplementary Fig. 9e). These results suggest that the activation of contralateral PL excitatory neurons attenuates anxiety-like behaviours and heat hyperalgesia induced by CFA.
Inhibition of PL excitatory neurons initiates anxiety. To ascertain the role of contralateral PL excitatory neurons in the initiation of anxiety-like behaviours, we unilaterally transduced PL excitatory neurons with AAV5 that carried the third generation of halorhodopsin (NpHR3.0) under the control of the CaMKIIa promoter. NpHR3.0 is a light-driven chloride pump that hyperpolarizes neurons in response to 593 nm of yellow light. Continuous 593 nm yellow light illumination with an intensity of 6-9 mW decreased the firing rate of the excitatory neurons from 4.82 ± 0.44 to 1.94 ± 0.31 Hz (Fig. 5a,b). The unilateral inhibition of PL excitatory neurons significantly decreased the time spent in the open arms of the EPM (Fig. 5d,e) and the time in the centre of the OFT (Fig. 5f,g). Open-arm entries in the EPM tended to be fewer in number when PL excitatory neurons were unilaterally inhibited (Fig. 5e). However, the unilateral inhibition of PL excitatory neurons did not affect the PWL (Fig. 5c), suggesting that PL excitatory neurons exert different roles in physiological and pathophysiological states.
Cdk5 is activated in the contralateral PL post CFA. These results illustrate that the deactivation of contralateral PL excitatory neurons triggers anxiety-like behaviours and exacerbates heat hyperalgesia in the chronic pain model; however, the underlying mechanism remains unknown. Many protein kinases and ion channels are involved in the regulation of neuronal excitability. For example, Cdk5 is widely expressed in the nervous system and is involved in numerous physiological and pathological processes 20,21 . It has been reported that activation of Cdk5 in the peripheral nervous system promotes primary afferent nociceptive signalling 22,23 and influences synaptic transmission in the central nervous system 24 . Stress exposure increases anxietylike behaviours and Cdk5 activation in the basolateral amygdala 25 . The inhibition of septal Cdk5 blocks enhanced anxiety induced by prior stress 26 . To test whether Cdk5 is involved in the modulation of pain sensation and pain-related anxiety-like behaviours, we first examined Cdk5 and p-Cdk5 protein levels in the contralateral and ipsilateral PL, CG1 or IL 1 or 7 days after CFA injection. These results indicate that Cdk5 protein levels were not altered after CFA injection in any these three regions (Fig. 6a,b), whereas p-Cdk5 levels in the contralateral PL were increased for at least 7 days (Fig. 6a). No significant changes in p-Cdk5 levels were identified in the contralateral CG1 or IL or the ipsilateral PL, CG1 or IL (Fig. 6a,b), suggesting Cdk5 is specifically activated in the contralateral PL after CFA injection.
Knockdown of Cdk5 reverts the deactivation of PL. To further test whether Cdk5 is involved in the deactivation of contralateral PL excitatory neurons, we expressed an effective short hairpin RNA (shRNA) to Cdk5 in the contralateral PL prior to CFA treatment. One week after virus micro-infusion, CFA was injected in the left hind paw contralateral to the lentivirus (LV)-injected side. The LV that expressed the Cdk5 shRNA infected the PL and decreased both Cdk5 and p-Cdk5 protein levels (Fig. 7a-c).
We next examined the physiology of neurons following knockdown of Cdk5 by calculating the number of APs evoked by current steps, as described above. The decreased number of APs caused by CFA injection was rescued by micro-infusion of Cdk5 shRNA into the PL (Fig. 7d). The input-output curves obtained from neurons in Cdk5 knockdown rats exhibited a leftward shift compared with non-silence shRNA controls. This input-output curve indicated that neurons from the Cdk5 shRNA rats elicited more APs than neurons from non-silence shRNA rats 1 day after CFA injection. The current required to drive spike firing at 12.5 Hz was substantially smaller in the Cdk5 shRNA rats compared with the non-silence shRNA rats 1 day after CFA (Fig. 7e,f). The neurons from Cdk5 shRNA rats also had a less depolarized firing threshold compared with those from naive rats (Fig. 7g,h). The average frequencies and the amplitudes of sEPSCs from both groups were not significantly different, although we detected a slight difference in the cumulative distributions ( Fig. 7i-k), suggesting that synaptic transmission was intact. In addition, there were no significant differences in resting membrane potential or input resistance of neurons from the two groups (Supplementary Figs 3c,d). These results demonstrate that Cdk5 knockdown reverses the decreased intrinsic excitability of layer 2/3 pyramidal neurons in the contralateral PL 1 day after CFA, which supports our hypothesis that the deactivation of contralateral PL excitatory neurons 1 day after CFA is a result of the activation of Cdk5 signalling pathway.

Knockdown of Cdk5 attenuates CFA-induced pain and anxiety.
To directly test whether Cdk5 is responsible for CFA-induced behavioural impairments, we measured the PWL and tested the EPM and OFT after a contralateral or an ipsilateral Cdk5 shRNA infection. Consistent with the above results, following Cdk5 knockdown in the contralateral PL, the PWL, the time in the open arms, open-arm entries and the time in centre were augmented (Fig. 8a), whereas the ipsilateral PL did not affect these behaviours (Fig. 8b).
These results confirm our hypothesis that the deactivation of the contralateral PL excitatory neurons by Cdk5 activation is responsible for the initiation of pain-induced anxiety-like behaviours and the modulation of pain sensation.

Discussion
In the present study, we demonstrate that the intrinsic excitability of excitatory pyramidal neurons in layers 2/3 of contralateral PL is decreased 1 day after CFA injection to the hind paw, whereas synaptic transmission is enhanced. Optogenetic activation of contralateral PL excitatory neurons in CFA mice exerts analgesic and anxiolytic effects, whereas optogenetic inhibition of PL excitatory neurons induces anxiety-like behaviours without affecting pain sensation. Cdk5 is activated in the contralateral PL and Cdk5 knockdown in the contralateral PL by Cdk5 shRNA reverses the deactivation of contralateral PL excitatory neurons as well as the behavioural impairments induced by CFA. One potential interpretation based on our study is that in chronic pain states, the deactivation of the contralateral PL excitatory neurons by Cdk5 activation promotes CFA-induced anxiety-like behaviours and heat hyperalgesia, which indicates that the mPFC CaMKIIα-mCherry (7) CaMKIIα-NpHR-mCherry (9) CaMKIIα-mCherry (7) CaMKIIα-NpHR-mCherry (11) CaMKIIα-mCherry (6) CaMKIIα-NpHR-mCherry (9) CaMKIIα-mCherry (6) CaMKIIα-NpHR-mCherry (7) Off On Off is a key node of the circuitry involved in both pain and anxiety processing. Chronic pain is thought to be caused by aberrant neuronal responses along the pain transmission pathway from the dorsal root ganglion to the spinal cord, thalamus and cortex 27 . The sensitization of peripheral nociceptors leads to primary hyperalgesia and pain. However, the functional and morphological changes in the central nervous system significantly contribute to the maintenance of chronic pain and its comorbidities. In the present study, we demonstrate that the PL but not the CG1 or IL of the mPFC is involved in inflammatory heat hyperalgesia and anxiety-like behaviours, which indicates that the three main subdivisions of the mPFC present different roles in pain sensation and affective pain. There are intrinsic connections between the PL and IL 28 and previous studies of oscillatory neural activity in these regions suggest their interaction 29,30 , contributing to the complex functions of the mPFC. To identify a role for PL excitatory neurons, we both bilaterally damaged and optogenetically activated the IL and repeated the behavioural tests and showed that these manipulations had no effects on anxiety-like behaviours and pain sensation. Our results are consistent with a recent study demonstrating that activation of the PL-nucleus accumbens (NAc) pathway in a spared nerve injury model produces antinociceptive effects and reduces the affective symptoms of pain 31 . However, we cannot fully exclude the role of the IL because we did not test the role of IL excitatory neurons in naive mice.
Pain signalling is conveyed to the contralateral cortex from the spinal cord. In our study, only lesions of the contralateral, not ipsilateral PL attenuated CFA-induced anxiety-like behaviours and heat hyperalgesia, supporting our hypothesis that the contralateral mPFC controls initiation of anxiety-like behaviours modulation of chronic pain. Further electrophysiological studies indicated that the intrinsic excitability of the contralateral PL excitatory neurons decreased 1 day after CFA. Optogenetic activation of contralateral PL excitatory neurons exerted analgesic and anxiolytic effects, which were not observed following activation of ipsilateral PL excitatory neurons. These results suggest that pain signalling is transmitted to the contralateral PL, where it results in decreased intrinsic excitability, with the ipsilateral side largely unaffected. However, the activation of either contralateral or ipsilateral PL excitatory neurons increased travel distance in the OFT, which suggests a general role for the PL in locomotor activity.
To gain insight into the neurobiological mechanisms of highorder sensation and cognitive functions, it is important to understand the critical transformational properties of information input and output in the mPFC, as well as the micro-circuitry formed in the mPFC. In this study, we focused on layer 2/3 pyramidal neurons, which are directly associated with pain sensation and pain-related behaviours [32][33][34] . We demonstrated that layer 2/3 pyramidal neurons of the PL are critical for integration and transmission in the pathological process of inflammatory pain. The intrinsic excitability of layer 2/3 neurons was decreased, whereas the synaptic transmission was increased 1 day after CFA injection. We speculate that when pain occurs, pain-related information from peripheral nociceptors is continuously transmitted to the PL, which leads to an increased synaptic transmission. However, as pain persists and becomes chronic, the intrinsic excitability of layer 2/3 pyramidal neurons in the PL decreases because of the continuous activation by inflammatory stimuli. Neurons with decreased intrinsic excitability fail to generate APs, which indicates that the integration and output of these neurons is affected. This dysfunction of layer 2/3 neurons in PL blocks the processing and transmission of the pain signalling, which in turn, initiates anxiety-like behaviours and exacerbates chronic pain. The regulation of pain in layer 2/3 pyramidal neurons of the PL interprets one potential mechanism of pain and pain-related anxiety in the central nervous system. Here, for the first time, we demonstrated the relationship of the deactivation of contralateral PL excitatory neurons, heat hyperalgesia and anxiety-like behaviours.
Moreover, our work identifies the activation of the Cdk5 signalling pathway as a potential mechanism underlying the deactivation of contralateral PL excitatory neurons, which suggests that Cdk5 acts as a key negative regulator of neuronal excitability in the PL. This finding is consistent with a previous study that neurons in the NAc from CaMKII-Cre Cdk5 conditioned knockout mice exhibit increased intrinsic excitability 35 . However, how Cdk5 negatively regulates intrinsic excitability remains unknown. The intrinsic excitability of neurons is driven by dynamic modulation of ion channel expression, localization and/or function 36 , which can be mediated by the direct or indirect phosphorylation of Cdk5. A previous study has shown that mGluR1 and GABA A receptors are involved in the deactivation of medial prefrontal cortical neurons in an arthritis pain model 14 . The potential candidates that act downstream of Cdk5 should also be involved in the firing of APs. Future studies must be performed to elucidate the additional mechanisms by which Cdk5 may negatively regulate the intrinsic excitability of PL excitatory neurons.
There are three issues to be noted: first, both chemical lesion and optogenetic activation of the contralateral PL exerted analgesia and anxiolytic effects. The results from the chemical lesion and optogenetic studies appear contradictive. The mPFC consists of a heterogeneous collection of neurons, including excitatory pyramidal neurons and local GABAergic interneurons 37 . In a chemical lesion, all PL neurons, including excitatory and inhibitory neurons, are eliminated, whereas the optogenetics manipulation only activated excitatory neurons. Evidence suggests that GABAergic interneurons are involved in the modulation of excitatory neuron activity in the PL 38,39 . This contradiction suggests that inhibitory neurons may also play a role in the modulation of anxiety-like behaviours and pain sensation. The role of GABAergic interneurons in chronic pain needs to be further clarified. Second, optogenetic activation of contralateral PL excitatory neurons in CFA mice not only increased the time in the centre but also the travel distance, which raises the question of whether the relief of anxiety-like behaviours is a result of the increased travel distance. The increased distance is consistent with previous work showing that inhibition of GABA synthesis in the PFC increases locomotor activity during a 24-h testing period 40 . It has been reported that the PFC has connections with motor structures, enabling a direct translation of PFC function outcome into behaviour 41 and may be the reason why the distance is increased with the activation of contralateral PL excitatory neurons. Our experiments further demonstrated that optogenetic activation of ipsilateral PL excitatory neurons in CFA mice only increased the travel distance without alleviating the anxiety-like behaviours. These results rules out the possibility that the relief of anxiety-like behaviours is because of the increased travel distance. Third, optogenetic inhibition of PL excitatory neurons did not influence the pain sensation. Previous studies have suggested that the PFC is involved in thalamic-PAGdorsal horn top-down modulation of pain 42  the activation of PL excitatory neurons strongly activates the descending inhibitory pathway, which thus increases the pain threshold. This would account for the finding that optogenetic inhibition of PL excitatory neurons did not influence pain sensation.
Nevertheless, our findings provide novel insights into the role of contralateral PL excitatory neurons in the regulation of pain sensation and affective pain. Cdk5 signalling is one potential mechanism responsible for the PL changes. Furthering our understanding of the underlying mechanisms of chronic pain may offer better therapeutic methods that target multiple aspects of pain with one treatment.

Methods
Experimental animals. Male Sprague-Dawley rats (200-250 g) and male C57BL/6J (20-25 g) mice were used, which were supplied by the Animal Center of Peking University, Health Science Center and the Guangdong Medical Laboratory Animal Center, respectively. The animals were housed in a constant temperature at 23 ± 1°C under a 12 h light/dark cycle. Food and water were available ad libitum. The animals were acclimated for at least 5 days before the beginning of the experimental procedures. All experimental procedures comply with the guidelines of the Animal Care and Use Committee of Peking University. CFA (100 ml for rats, 10 ml for mice, Sigma-Aldrich, St Louis, MO, USA) was injected into the plantar surface of the hind paw, and the animals without CFA injection comprised the naive group.
Assessment of thermal hyperalgesia. Thermal hyperalgesia was evaluated by following a thermal stimulus paradigm adapted from published reports of ref. 43. Before testing, the animals were allowed to acclimatize to the environment for 20 min. The radiant heat source was adjusted to a range of 12-15 s for rats and 5-10 s for mice as the baseline latencies with a cutoff time of 30 s to prevent tissue damage. To record the PWL in response to the heat stimulus, each hind paw was measured four times with a 5-min interval, and the mean value was recorded. The experimental procedures were performed in a double-blind manner. Open field test. The apparatus consisted of a large area composed of plastic, surrounded by walls that were 100 cm high. The floor was 100 Â 100 cm for rats and 50 Â 50 cm for mice 44 ; the overall illumination was 100-200 lux. Each animal was gently placed in the centre of the open field, and its behaviour was videotaped. The time in the centre (rats, 60 Â 60 cm; mice, 25 Â 25 cm) and the distance the animals travelled were measured using ANY-maze (Stoelting Co., IL, USA).
Lesions of the PL, CG1 and IL. The rats were anesthetized with 10% chloral hydrate (0.4 g kg À 1 , i.p.) and positioned in a stereotaxic instrument (RWD, Shenzhen, China). A 5-ml Hamilton microsyringe was unilaterally placed in the mPFC sub-regions according to the atlas of Paxinos and Watson (1997) (CG1: AP, þ 2.8, ML, ± 0.5, DV, À 2.6; PL: AP, þ 2.8, ML, ± 0.5, DV, À 4; IL: AP, þ 2.8, ML, ±0.5, DV, À 5 mm). For each side of the PL, CG1 and IL, a 0.5 ml volume of a 0.1-M solution of QA in phosphate buffered saline (0.1 mol l À 1 , pH ¼ 7.4) was administered in 1 min (0.5 ml min À 1 ). All injections were followed by an additional 2 min to allow diffusion before removal of the injection needle. After the surgery, the animal was returned to its home cage. One week after the surgery, anxiety-like behaviours and PWL were assessed.
Voltage and current signals were recorded from layer 2/3 neurons using an Axon 200B amplifier (Axon Instruments, CA). The spike firing pattern of the AP was used to electrophysiologically identify pyramidal neurons, which exhibited significant spike frequency adaptation in response to a depolarization current. The APs were recorded using the current-clamp mode. For sEPSC recordings, picrotoxin (50 mM) was added to block GABA A receptor-mediated inhibitory synaptic currents. The sEPSCs were recorded using the voltage-clamp mode and neurons were voltage clamped at À 70 mV. The series resistance (Rs) was monitored at regular intervals throughout the recording experiment. Cells with Rs larger than 25 MO during the recordings were discarded. Data were acquired and analysed with the Axoclamp 200B amplifier and pCLAMP software (Axon Instruments, Foster City, CA, USA). The analysis of sEPSCs was performed blind using MiniAnalysis software (Synaptosoft). The average amplitude and frequency of sEPSCs was determined by the two-tailed t-tests. 50 random points selected from each cell were concatenated to describe the cumulative distributions of sEPSC in each condition and then compared by a Kolmogorov-Smirnov two sample test. Po0.05 was considered to be statistically significant. Data are presented as mean ± s.e.m.
Multi-channel recordings and behavioural tests were performed at least 4 weeks later to enable viral expression. In behavioural tests, the mice were placed in the centre of the plus maze or open field and allowed to freely explore for 3 min; light was subsequently delivered for 3 min and was shut-off for the next 3 min. The PWL was measured every 3 min for four times before light stimulation, with light stimulation and after light stimulation, respectively. The mean value was calculated. For the activation of the excitatory neurons, 20 Hz, 6-9 mW 473 nm blue light was delivered by a blue light laser (MBL-473/200 mW; Fiblaser, Shanghai, China), while for the inhibition of the excitatory neurons, continuous 6-9 mW 593 nm yellow light was delivered by a yellow light laser (MBL-593/200 mW; Fiblaser, Shanghai, China).
Multi-channel recordings. The optrode was an optic fibre attached with four surrounding tetrodes. The fibre tip was 0.5 mm shorter than the tetrode tips. The input end of the fibre was embedded into a ceramic ferrule, which could be connected to the laser source via an FC/PC connector. The tips of all tetrodes (12.7 mm nickelchromium wires, CFW, CA, USA) were plated with platinum (chloroplatinic acid solution) to a final impedance of 0.5-0.6 MO. The mice were anesthetized with 0.5% pentobarbital sodium and positioned in a stereotaxic frame. The multi-channel optrode was injected in the PL (AP, þ 1.9, ML, À 0.3, DV, À 2.3 mm). The baseline firing of the PL neurons was recorded by an OmniPlex D Neural Data Acquisition System for 1 min, followed by six rounds of 30 s light stimulation and 30 s light off. Continuous wide-band data were imported into Plexon Offline Sorter software (Plexon, Inc., Dallas, TX, USA) for the spike detection and offline sorting.
Western blotting. The rats were anesthetized with 10% chloral hydrate (0.4 g kg À 1 , i.p.) and the brains were quickly removed and frozen in N-hexane À 70°C for B40 s. Bilateral tissue punches of the PL, IL and CG1 were obtained from 60-mm thick sections taken on a sliding freezing microtome 45 . Western blotting experiments were performed according to the protocols previously described 23 . In brief, tissues were homogenized in ice-cold lysis buffer (50 mM Tris, pH 7.4, 150 mM NaCl, 5 mM EGTA, 0.5% NP-40, 10 mM NaF, and 1 mM PMSF) and rotated at 4°C for 1 h before the supernatant was extracted. The supernatant was extracted by centrifugation at 12,000g at 4°C for 5 min. Equal amounts of protein extracts were denatured and subjected to SDS-polyacrylamide gel electrophoresis. After separation, proteins were transferred to nitrocellulose membranes (Bio-Rad). The membranes were blocked with 5% nonfat milk in TBST (25 mM Tris, pH 7.4, 137 mM NaCl, 2.7 mM KCl, and 0.05% Tween 20) for 1 h at room temperature and incubated with goat monoclonal anti-p-Cdk5 (1:100 dilution, Sc-12918, Santa Cruz Biotechnology, Dallas, TX, USA), monoclonal anti-Cdk5 antibody (1:2,000 dilution, Upstate Biotechnology, Buffalo, NY, USA) or monoclonal anti-b-actin antibody (1:2,000 dilution, Sigma-Aldrich, St Louis, MO, USA) overnight at 4°C. After washing three times with TBST, the membranes were incubated with secondary antibody (1:2,000 dilution) overnight at 4°C, then washed again, and finally developed with ECL solutions (Santa Cruz Biotechnology, Dallas, TX, USA).
Micro-infusion PL of Cdk5 ShRNA. Surgery was performed according to the protocol described above. ShRNA LVs that co-expressed EGFP and shRNAs against rat Cdk5 were purchased from Shanghai GeneChem Co., Ltd. The target mRNA sequence was as follows: CCAAACUGCCAGACUAUAA. LVs that expressed shRNAs that targeted a non-specific sequence (TTCTCCGAACGTGT-CACGT) were used as the controls. One week after the surgery, whole-cell patch recordings were performed and behaviours were assessed.
Statistical analysis. The data are presented as means ± s.e.m. Comparisons between two groups were performed using Student's unpaired two-tailed t-test or paired t-test. Comparisons between three groups were performed using one-way ANOVA with Newman-Keuls post tests. Comparisons between two groups with different time points were performed using two-way ANOVA with Bonferroni post tests. The criterion for statistical significance was Po0.05, and differences were calculated using GraphPad Prism 5.0. 45. Xu, Y. et al. Essential role of NR2B-containing NMDA receptor-ERK pathway in nucleus accumbens shell in morphine-associated contextual memory. Brain research bulletin 89, 22-30 (2012).