The emergence of adolescent onset pain hypersensitivity following neonatal nerve injury
© Vega-Avelaira et al; licensee BioMed Central Ltd. 2012
Received: 23 December 2011
Accepted: 24 April 2012
Published: 24 April 2012
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© Vega-Avelaira et al; licensee BioMed Central Ltd. 2012
Received: 23 December 2011
Accepted: 24 April 2012
Published: 24 April 2012
Peripheral nerve injuries can trigger neuropathic pain in adults but cause little or no pain when they are sustained in infancy or early childhood. This is confirmed in rodent models where neonatal nerve injury causes no pain behaviour. However, delayed pain can arise in man some considerable time after nerve damage and to examine this following early life nerve injury we have carried out a longer term follow up of rat pain behaviour into adolescence and adulthood.
Spared nerve injury (SNI) or sham surgery was performed on 10 day old (P10) rat pups and mechanical nociceptive reflex thresholds were analysed 3, 7, 14, 21, 28, 38 and 44 days post surgery. While mechanical thresholds on the ipsilateral side are not significantly different from controls for the first 2–3 weeks post P10 surgery, after that time period, beginning at 21 days post surgery (P31), the SNI group developed following early life nerve injury significant hypersensitivity compared to the other groups. Ipsilateral mechanical nociceptive threshold was 2-fold below that of the contralateral and sham thresholds at 21 days post surgery (SNI-ipsilateral 28 (±5) g control groups 69 (±9) g, p < 0.001, 3-way ANOVA, n = 6 per group). Importantly, no effect was observed on thermal thresholds. This hypersensivity was accompanied by macrophage, microglial and astrocyte activation in the DRG and dorsal horn, but no significant change in dorsal horn p38 or JNK expression. Preemptive minocycline (daily 40 mg/kg, s.c) did not prevent the effect. Ketamine (20 mg/kg, s.c), on the other hand, produced a dose-dependent reversal of mechanical nociceptive thresholds ipsilateral to the nerve injury such that thresholds return to control levels at the highest doses of 20 mg/Kg.
We report a novel consequence of early life nerve injury whereby mechanical hypersensitivity only emerges later in life. This delayed adolescent onset in mechanical pain thresholds is accompanied by neuroimmune activation and NMDA dependent central sensitization of spinal nociceptive circuits. This delayed onset in mechanical pain sensitivity may provide clues to understand the long term effects of early injury such as late onset phantom pain and the emergence of complex adolescent chronic pain syndromes.
It is well documented that neuropathic pain is absent or transient in the youngest infants or children. Brachial plexus injuries at birth, followed by nerve repair, are not associated with pain  and reports of phantom pain, complex regional pain syndrome, peripheral neuropathy pain are very rare before 5–6 years of age . This is supported by animal models of neuropathic pain, spared nerve injury (SNI) and chronic constriction injury (CCI), where little or no allodynia and pain behaviour is observed in animals whose nerves have been injured before three weeks of age or postnatal day 21 (P21) [3–5].
The aim of the current study was to investigate the longer term effects of early nerve injury and to test whether pain or hypersensitivity might emerge beyond the post injury period, perhaps only in adolescence. To date, the longer term effects of nerve injury, and the possibility of emergence of pain beyond childhood has not specifically been addressed [6–8]. Most studies of nerve injury in infants have not followed up the long term consequences; obstetric injuries in man have been followed up for only for about 7 years and experimental nerve injury rat pups, only for a few weeks . Intriguing clues exist in the clinical literature that symptoms may appear later in life. Thus, when Melzack and colleagues studied phantom limb pain in adolescents with either congenital or early surgical loss of limbs, they noted that onset of phantoms in those with the earliest loss were remarkably delayed – emerging only after a mean of 7 years . The possibility that nerve injury in childhood could cause a delayed onset pain syndromes is interesting in view of the onset of unexplained pain syndromes such as complex regional pain syndrome (CRPS) in adolescence .
We have carried out a longitudinal study of pain behaviour and immune responses into adulthood, following “spared nerve injury” (SNI) in young rats. We have observed that while young rats fail to display neuropathic behaviour for the first weeks after nerve injury, at adolescence they develop lasting cutaneous mechanical hypersensitivity as a consequence of this early-life nerve injury.
Surgery was performed on adult (8 weeks old) male Sprague–Dawley rats and rat male pups (10 days postnatal age, P10) and carried out in accordance with the United Kingdom Animal (Scientific Procedures) Act 1986. Spared nerve injury (SNI) and sham surgery were performed under (4 %) halothane general anaesthesia with antiseptic conditions as described previously . After skin preparation, the sciatic nerve and its three terminal branches were exposed in the upper lateral thigh. The common peroneal and tibial branches were cut and ligated under direct vision, leaving the sural nerve intact. Muscle and skin were closed in two layers. In sham operations, the procedures were the same but the nerves were only exposed and not cut or ligated. In all cases great care was taken neither to stretch the nerve or its branches nor to damage the intact nerves.
After surgery, animals were returned to their cages and litters and maintained on a 12 hour light/dark cycle at constant ambient temperature with free access to food and water until the next procedure (behaviour or tissue collection for immunostaining).
Rats that had undergone spared nerve injury (SNI) or sham surgery at P10 were tested for cutaneous mechanical sensitivity at 3, 7, 14, 21, 28, 38 and 44 days post surgery (n = 6 per group). Flexion withdrawal reflex thresholds in response to punctate mechanical stimulation of the dorsolateral surface of the hindpaw was tested using calibrated von Frey filaments (VF), that exert a reproducible stimulus strength in grams (Stoelting, Woodvale, IL). The dorsolateral surface of the hindpaw is innervated by the sural nerve, and this test is known to reveal mechanical allodynia in the adult rat after SNI surgery . Filaments were applied sequentially to the plantar surface of the hind paw six times at intervals of 1 s. Response threshold was defined as the VF filament which produced reflex paw withdrawal in 4 out of 6 applications.
Rats that had undergone spared nerve injury (SNI) or sham surgery P10, were also tested for thermal cutaneous sensitivity at 3, 7, 14, 21, 35, 45 and 51 days post surgery (n = 6 per group). The lateral plantar surface was exposed to a beam of radiant heat through a transparent Perspex surface (Hugo Basile Inc.) . The flexion withdrawal reflex latency was recorded, with a minimal value of 0.5 s and a maximum of 15 s. The heat stimulation was repeated 3 times at an interval of 5–10 min for each paw and the mean calculated.
Rat pups (n = 6) received a 40 mg/kg i.p. minocycline, a dose which reverses mechanical allodynia after nerve injury in adults . The first injection was administered the day before (P9) SNI surgery, the second just prior to surgery at P10 and this was followed by daily ip injections of minocycline until 21 days post surgery (P31). Two control groups were used (i), a group of SNI animals injected with saline (n = 6), and (ii) a group of sham surgery animals, injected with either saline (n = 6) or minocycline (n = 6). The animals were tested for mechanical pain thresholds using calibrated von Frey hairs. The test was carried out by a blinded observer: the animals were tagged with a chip applied subcutaneously to avoid any identifiable external marks and the animals were given to the observer in a random order. The data was collected for analysis by ANOVA.
Young adult rats (P31) that had undergone SNI (n = 6) or sham (n = 6) surgery at P10 were treated with subcutaneous ketamine (Sigma) in cumulative doses of 1, 10 and 20 mg/Kg in a volume of 250 μl as described elsewhere . Doses were administered at intervals of one hour. Two methods were used: 1) Change in response frequency to a threshold mechanical stimulus, where the frequency of paw withdrawal before and after ketamine injection in response to the same, threshold von Frey hair applied to the dorsolateral area of the paw, was compared. The mean mechanical threshold was significantly different in the ipsilateral SNI group (31 ± 6 g) and the control groups (67 ± 4 g), (ANOVA p < 0.01, Tukey p < 0.05). The data is expressed as a percentage of responses to the corresponding baseline mechanical threshold, plotted using average and standard error of the mean and statistically analysed using a 2-way ANOVA. 2) Change in mechanical pain thresholds measured with a dynamic plantar aesthesiometer (Ugo Basile). Animals were habituated in Perspex cages with a mesh floor and the aesthesiometer probe applied in the lateral plantar surface of the paw within the territory innervated by the sural nerve . The intensity of the stimulus increased from 0 to 50 g in 30 seconds and the average threshold taken from two applications. Mechanical sensitivity thresholds were established before (baseline) and one hour after each dose administration and a final measurement was performed at 72 hours post ketamine administration (after ketamine clearance).
Tissue was extracted from rats that had undergone surgery at P10 or as adults at 7 and 30 days (P10 only) post surgery. Rats were overdosed with 100 mg/kg of Euthanal® and perfused through the heart with 200 ml heparin-saline, followed by 200 mL 4 % paraformaldehyde in 0.1 M phosphate buffer (PB). The L4–L5 lumbar spinal cord and the corresponding L4 and L5 ganglia were removed and postfixed in 4 % paraformaldehyde for 1 h at 4°C followed by immersion in 30 % sucrose in 0.1 M of PB at 4°C for at least two days before sectioning. Serial, 20 μm cryostat sections were cut and stained after blocking in 10 % normal goat serum, 0.3 % Triton X in 1× PBS using primary antibodies: Rabbit anti-IBA-1 (1/1000, Wako®), mouse anti NF200 (1/1000, Chemicon®), and rabbit-anti-GFAP (1/100 Dako®). The antibodies were incubated overnight at room temperature in 3 % normal goat serum, 0.3 % Triton X in 1× PBS. Secondary antibodies were goat anti-mouse (Alexa-488®) and goat anti-rabbit (Alexa-593®) at 1/200 dilution in 3 % normal goat serum, 0.3 % Triton X in 1× PBS. Antibody excess was removed by 3 washes in PBS for 10′ at RT. The isolectin IB4 (Bandeira simplicifolia) labelled with FITC (Sigma®) was used to identify the non-peptidergic neurons . After staining, the sections were kept for 16 h in the dark to normalize the background and then microscope images acquired at 10X magnification with OpenLab® software at a constant exposure time of 1.02″.
The images generated by immunohistochemistry were analysed with Image J 1.36 (NHS) software, n = 3 rats per experimental group, n = 4-6 sections spinal cord or ganglia per animal. In the spinal cord, microglia (IBA-1 positive;  or astrocytes (GFAP positive; ) were counted in the region of loss of IB4 staining, which delineates the area of termination of lesioned nerve in the SNI model on the ipsilateral and equivalent contralateral side . Data is expressed as fold difference of the contralateral side and analysed using 2-way ANOVA and plotted using average and standard error of the mean.
In the ganglion, sections were stained with IBA-1 to label macrophages  and with NF200 to label large neurons . Representative sections from the centre of the ganglion, 160 μm apart, were used for analysis. Macrophage activation was assessed as previously described , by counting neurons with enlarged macrophages and processes clustering around the NF200 + ve neuronal cell bodies in characteristic 'ring-like' structures. Data was expressed as percentage of large NF200 positive neurons with IBA-1 positive macrophage ring-like structures and analysed using 2-way ANOVA and plotted using average and standard error of the mean.
The dorsal horn quadrant (ipsilateral or contralateral) of L3–L5 spinal cord segments was snap frozen in liquid nitrogen after extraction and stored at -80o C until further procedure. Proteins were extracted in 150 μL RIPA buffer (NP-40 1 %, Hepes 20 mM, pH 7.2, NaF 100 mM; NaCl 100 mM, NaVO 1 mM, EDTA 5 mM, and 1 % of protease inhibitor) from Sigma by blender homogenisation, incubated for 2 h on ice and centrifuged at 12,000 g to remove the debris. The proteins were diluted to yield 1 mg/mL and stored in aliquots at -80o C. 10 μg of total protein were used for the electrophoresis with the Mini Protean 3 Cell System (Bio-Rad) with 10 % acrylamide precast Ready gels (Bio-Rad). Electrophoresis was carried out in Tris 20 mM, glycine 247 mM, and 0.0001 % SDS buffer at 4o C until the reference colorant reached the end of the gel. The Rainbow coloured protein ladder from Amersham was loaded to monitor the electrophoresis. The transference blots to the PVDF membranes (Bio-Rad) were done in Tris 48 mM, glycine 77 mM, 0.0001 % SDS, and 10 % of methanol for 1.5 h at 4o C. Following the blot, membranes were blocked in PBS solution (PBS tablets, Sigma) with 0.1 % Tween 20 (Sigma) and 4 % semi-skimmed milk powder (Sainsbury’s). The primary antibodies were incubated at 4o C overnight with gentle shaking and diluted in blocking buffer (rabbit anti-phospho-p38 or rabbit anti-phospho-JNK at 1:1000 from Cell Signaling and mouse anti-GAPDH from Chemicon at 1/2000). Secondary antibodies from Santa Cruz were used at a dilution of 1/2000. Antibody excess was removed with six washes in PBS/0.1 % Tween 20. To reveal the signal we used the ECL western blotting detection system from Amersham and the images were acquired with the Quantity One system (Bio-Rad). The intensity of the western blots bands for phospho-p38 (~40 kDa), phospho-JNK (~46 and ~54 Kda bans) and GFAP (~50 kDa) were measured with Quantity One, v4.6.2 (Bio Rad) densitometry using GAPDH (36 kDa band) housekeeping gene for normalization. Values were expressed as the ratio “densitometry protein/densitometry GAPDH”.
To analyse the long term consequences of early-life nerve injury in pain behaviour we carried out a longitudinal study of rats that had undergone spared nerve injury (SNI) or sham operations when they were 10 days old (P10).
Figure 1B shows the same longitudinal study on radiant heat nociceptive thresholds, post P10 SNI surgery. As reported elsewhere [22, 23], thermal thresholds tend to fall with postnatal age. However, in contrast to the effect on mechanical nociception, analysis of thermal nociceptive thresholds shows no significant differences in the SNI group when compared to the control groups throughout the longitudinal study up to P54. (Figure 1B).
In the light of the known relationship between glial activation and hyperalgesia [24–26], we analysed the time course of activation of microglia and astrocytes in the spinal cord and macrophages in dorsal root ganglia following early life nerve injury [27–29]. Glial activation was examined in rats, which had undergone SNI surgery at P10 rat pups, at two postnatal time points. The first was at 7 days post surgery (P17), when there was no change in mechanical sensitivity and the second was at 21 days post surgery (P31) when mechanical hypersensitivity had developed and both were compared with sham groups. In addition, we included a group of rats that underwent surgery as adults, 7 days post surgery as a positive control of glia activation .
In adult models of nerve injury induced neuropathic pain, microglial activation is accompanied by phosphorylation of p38 and this is well known marker of microglia activation after adult nerve injury . Furthermore, this phosphorylation of p38 after adult nerve injury is known to be inhibited by minocycline [35, 36]. However, interestingly, we did not find any differences in dorsal horn phospho-p38 levels between the SNI-saline and sham groups 21 days post surgery (P31), despite the presence of activated microglia and behavioural hypersensitivity (Figure 5). Figure 5 also shows the phospho-p38 levels in SNI-minocycline treated animals are not significantly different to the SNI-saline or sham groups (Figure 5B and C).
We also analysed the phosphorylation of c-Jun N-terminal kinase (JNK) which is a marker of astrocyte activity after nerve injury and required for maintenance of neuropathic pain [37, 38]. We did not find any significant difference when comparing the SNI-saline and sham groups (Figure 5C and D) but minocycline had a small (1.5 fold) but significant effect up on the SNI group p < 0.001, 1-way RM-ANOVA, n = 4 per group).
The ability of ketamine to reduce mechanical hypersensitivity was also measured using the frequency of paw withdrawal threshold after mechanical noxious stimulation with von Frey filaments (VF). The results show a significant (p < 0.001, 3-way ANOVA, n = 6 per group) reduction in the frequency of paw withdrawal at the ketamine doses of 10 mg/Kg (to 52 % ±6) and 20 mg/Kg (to 45 % ±11) (Figure 6B).
In this study we have analysed the long term consequences of early-life nerve injury upon pain behaviour in the rat. We have demonstrated for the first time that early life nerve damage produces a mechanical hypersensitivity that only emerges in adolescence. In contrast to the rapid and profound allodynic effects in adults [11, 40], spared nerve injury at postnatal day 10 has little or no effect upon pain behaviour in the first weeks after surgery. However, if threshold testing is extended to 3 weeks after the surgery, a mechanical hypersensitivity on the ipsilateral hindpaw emerges which is maintained into adult life. This hypersensitivity was not observed on the contralateral paw or following sham injury. Moreover, no differences were observed in thermal nociceptive thresholds in these animals ruling out a non-specific motor deficit and suggesting that early life spared nerve injury has a specific effect upon adult mechanical nociception.
Mechanical pain thresholds steadily increase through postnatal development due to fine tuning of spinal pain circuits  and the maturation of spinal inhibitory networks . This steady rise is also observed in animals after nerve lesion  but only while the animal is still young. However, at the onset of the adolescence, from P30 onwards , this steady rise stops on the nerve injured side such that a significant 2-fold decrease in mechanical pain thresholds emerges leaving the adult animal with a selective mechanical, but not thermal hypersensitivity on the affected side.
Clinically, there are few studies on the long term effects of peripheral nerve injury in infants. While neuropathic pain is not reported in young patients following infant brachial nerve plexus avulsion [1, 44], self-mutilation is more frequent in these children  due to either the subsequent post trauma surgery or the initial nerve injury or both. Perhaps more relevant, it has been reported that the appearance of phantom syndromes (many of which are painful) following loss of limbs in infancy, do not appear for many years after the original loss, in some cases up 3 to 15 years later [9, 46]. This delayed onset pain after early nerve injury may also contribute to chronic complex pain syndromes with cutaneous sensory abnormalities which arise in adolescence, but whose aetiology is unknown [10, 47]. The animal model described here might cast some light on such syndromes, revealing as it does, the possibility for hypersensitivity to arise a considerable time after an original injury in infancy.
One possible mechanism underlying this emergence of mechanical sensitivity might lie in the neuroimmune system. Glial activation is a common characteristic of adult neuropathies [25, 26] and several studies have demonstrated the need for microglial/macrophage activation to initiate the neuropathy in the adult rodent [13, 27, 28]. We have previously demonstrated that there is little activation of either both spinal microglia [30, 31] or macrophages in the dorsal horn  in the young P10 rat after 7 days post nerve injury and our recent transcriptome analysis of the dorsal root ganglia and the dorsal horn at different ages reveals a much greater and different profile of immune related genes regulated in the adult compared to young rats after nerve injury [21, 48]. Since it is well known that the immune system goes through dramatic changes of maturation through the postnatal development [49, 50], we hypothesized that a late onset change in microglia/macrophage activation was the trigger for the emergence of mechanical hypersensitivity in adolescence. Consistent with this proposal, our results showed that microglia, astrocytes and macrophages are only activated after early life nerve injury at the onset of the adulthood (at P30), the same time point at which mechanical hypersensitivity emerges. However, importantly, microglial activation was not accompanied by an increase in phosphorylated p38 expression at the onset of the adulthood (at P30) after early life nerve injury when compared to the baseline levels of phosphorylation in the sham operated group. While p38 phosphorylation is a key event in microglia activation when the nerve injury is sustained in adult animals, our results indicate that the p38 map kinase pathway is not involved in this late onset of microglia activation after early in life nerve injury. This would explain why preemptive minocycline (a p38 inhibitor [35, 36]), at a dose designed to maximise its suppression of macrophage/microglial activation  did not prevent or even reduce the delayed onset adolescent mechanical hypersensitivity.
It has been proposed that astrocytes have a key role in the maintenance of neuropathic pain in adults  and that microglia activation is required for the activation of astrocytes [51, 52]. Interestingly, we also observed astrogliosis at onset of adulthood (P30), but similarly to microglia, we did not find differences in JNK phosphorylation (a marker of astrocyte activation) at the onset of the adulthood (at P30) after early life nerve injury when compared to the baseline levels of phosphorylation in the sham operated group. The small effect of minocycline upon JNK phosphorylation was evidently not sufficient to ameliorate the mechanical hyperalgesia.
Despite the rise in activation of microglia and astrocytes at the onset of the adulthood (at P30) after early life nerve injury, our results suggest that this activation must involve different signalling pathways to those classical map kinase pathways found when the injury is sustained in the adulthood [28, 37]. We cannot rule out the possibility of a different role for glia in this model of early in life nerve injury. In this way, microglia is a heterogeneous group with many functions that include surveillance (resting microglia), toxicity (classical activation associated with pro-inflammatory cytokines), neuroprotection (alternative activation associated with anti-inflammatory cytokines and repair) [53–55]. Thus, it could be possible that glia has a different role in this model where microglia activates towards a healing process with the astrocyte support. Our results show that microglia is not activated after nerve injury as it would be expected for a repair phenotype. Instead, microglia activation begins at the onset of adult hood 3 weeks after the initial insult and is accompanied by mechanical hypersensitivity. The experimental models of neuropathic pain in adult clearly show that microglia activation has pro-inflammatory phenotype [56, 57] and this activation is directly linked to initiation of pain behaviours . Thus, our results are more in accordance with a role of microglia in triggering mechanical hypersensitivity. Nevertheless, we consider that further analysis is required to understand the role and mechanisms of microglia and astrocytes activation in this model of early in life nerve injury.
To explore the neuronal mechanisms that might underlie this novel mechanical hypersensitivity following early life nerve injury we have explored a classic mechanism that underlies maintained neuropathic mechanical allodynia in adult nerve injury models, namely NMDA mediated central sensitization . Central sensitization is a well-established mechanism whereby dorsal horn neuronal activity is enhanced due to increased membrane excitability as a result of opening voltage sensitive NMDA channels allowing Ca2+ entry into the cell . Activation of NMDA receptors is an essential step in both initiating and maintaining activity-dependent central sensitization  and the use of inhibitors such us ketamine can attenuate neuropathic allodynia in adults [14, 61]. In the present study, we have clearly demonstrated that ketamine applied when the rat reaches adulthood reverses the mechanical hypersensitivity following early life nerve injury to baseline levels. The mechanism by which this central sensitization only emerges three weeks after P10 nerve injury is not clear, but it is possible that it results from alterations in activity dependent maturation of dorsal horn inhibitory circuits  or descending controls of dorsal horn excitability .
The importance of early life events in individual disease susceptibility is well known but recognition that early pain experience may also predispose individuals to greater pain at a later stage of life is a more recent concept. Increasing evidence of the activity dependence and plasticity of both peripheral and central sensory connections in the neonatal period suggests that excess nociceptive input or tissue injury in infancy could lead to prolonged structural and functional alterations in pain pathways lasting into adult life [23, 64]. This is especially relevant to individuals who have experienced significant and repeated noxious stimulation as a result of surgery and intensive care in infancy . Such clinical procedures evoke robust behavioural and physiological responses at spinal cord and cortical level [4, 53] causing measurable hyperalgesia [5, 6, 52] and may leave a lasting susceptibility to pain in later life . The effects we report here are restricted to early life infant nerve injury which causes no sign of pain in the weeks, months and years after injury in humans and the same equivalent developmental period in rats. However, adolescence reveals a baseline hypersensitivity after early in life nerve injury that is similar to that seen in humans. Therefore, we provide a new insight to those mechanisms that contribute to chronic pain behaviours such as late onset of phantom syndromes.
In conclusion, we report here, a novel consequence of early life nerve injury whereby mechanical hypersensitivity only emerges later in life. This delayed adolescent onset in mechanical pain thresholds is accompanied by neuroimmune activation and NMDA dependent central sensitization spinal nociceptive circuits. This delayed onset in mechanical pain sensitivity may provide clues to understanding the long term effects of early injury such as late onset phantom pain and the emergence of complex adolescent chronic pain syndromes.
Spared Nerve Injury
Chronic constriction injury
Young sham group, ipsilateral side
Spared nerve injury
Mean intensity normalised.
We acknowledge the technical assistance of Mrs. Jacqueta Meredith-Middleton. This work was supported by the Wellcome Trust and the Medical Research Council (UK). The authors have no conflicts of interest with regard to the studies described in this manuscript.
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