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Although botulinum toxin type A (BoNT/A) is approved for chronic migraine treatment, its mechanism of action is still unknown. Dural neurogenic inflammation (DNI) commonly used to investigate migraine pathophysiology can be evoked by trigeminal pain. Here, we investigated the reactivity of cranial dura to trigeminal pain and the mechanism of BoNT/A action on DNI.
Because temporomandibular disorders are highly comorbid with migraine, we employed a rat model of inflammation induced by complete Freund's adjuvant, followed by treatment with BoNT/A injections or sumatriptan p.o. DNI was assessed by Evans blue‐plasma protein extravasation, cell histology and RIA for CGRP. BoNT/A enzymatic activity in dura was assessed by immunohistochemistry for cleaved synaptosomal‐associated protein 25 (SNAP‐25).
BoNT/A and sumatriptan reduced the mechanical allodynia and DNI, evoked by complete Freund's adjuvant. BoNT/A prevented inflammatory cell infiltration and inhibited the increase of CGRP levels in dura. After peripheral application, BoNT/A‐cleaved SNAP‐25 colocalized with CGRP in intracranial dural nerve endings. Injection of the axonal transport blocker colchicine into the trigeminal ganglion prevented the formation of cleaved SNAP‐25 in dura.
Pericranially injected BoNT/A was taken up by local sensory nerve endings, axonally transported to the trigeminal ganglion and transcytosed to dural afferents. Colocalization of cleaved SNAP‐25 and the migraine mediator CGRP in dura suggests that BoNT/A may prevent DNI by suppressing transmission by CGRP. This might explain the effects of BoNT/A in temporomandibular joint inflammation and in migraine and some other headaches.
These Tables list key protein targets and ligands in this article which are hyperlinked to corresponding entries in http://www.guidetopharmacology.org, the common portal for data from the IUPHAR/BPS Guide to PHARMACOLOGY (Pawson et al., 2014) and are permanently archived in the Concise Guide to PHARMACOLOGY 2013/14 (Alexander et al., 2013).
Botulinum toxin type A (BoNT/A) blocks the vesicular release of neurotransmitters by proteolytic cleavage of a synaptic protein, synaptosomal‐associated protein 25 (SNAP‐25). SNAP‐25 is a part of the synaptic protein complex which is involved in Ca2+‐dependent exocytosis (Kalandakanond and Coffield, 2001; Blasi et al., 1993). This effect of BoNT/A at peripheral nerve endings is the basis of its therapeutic use in a range of neuromuscular (blepharospasm, focal dystonia and spasticity) and autonomic disorders (hyperhidrosis and bladder dysfunction) associated with neuronal over‐activity (Dressler, 2013). Based on large clinical studies, pericranially injected BoNT/A has also been approved for the treatment of chronic migraine (Diener et al., 2010). It is widely accepted that migraine headaches involve activation of trigeminal afferents innervating the meningeal blood vessels and dural neurogenic inflammation (DNI) (Moskowitz, 1990; Geppetti et al., 2012; Ramachandran and Yaksh, 2014). We have recently found that the activation of dural afferents, measured as plasma protein extravasation, can be evoked by extracranial pain in the trigeminal region (orofacial formalin‐evoked pain and infraorbital nerve constriction‐induced trigeminal neuropathy) (Filipović et al., 2012, 2014). The plasma protein extravasation induced by different types of pain was prevented by peripherally injected BoNT/A. The effect of BoNT/A in the cranial dura was associated with axonal transport of the toxin, because its effects were prevented by injection of colchicine directly into the trigeminal ganglion (Filipović et al., 2012).
In the present study, we investigated the effects of BoNT/A in a model of trigeminal pain induced by complete Freund's adjuvant (CFA) injection into the temporomandibular joint (TMJ), a common model of temporomandibular disorders (Harper et al., 2001; Villa et al., 2010). Temporomandibular disorders involve dysfunction of both the TMJ and masticatory muscles, leading to chronic pain (De Rossi et al., 2014). BoNT/A injections into masticatory muscles have been reported to reduce the tenderness and pain in patients suffering from temporomandibular disorders (Sunil Dutt et al., 2015). Severe forms of temporomandibular disorders are highly comorbid with primary headaches – up to 86% of patients suffer from migraine or other primary headaches (Bevilaqua Grossi et al., 2009; Franco et al., 2010). The underlying mechanism of the comorbidity is proposed to be related to extensive innervation of cranial dura by mandibular branch of trigeminal nerve (Schueler et al., 2013). So far, inflammation of the TMJ has been used preclinically to study the trigeminal sensitization associated with migraine (Villa et al., 2010; Thalakoti et al., 2007). CFA injection into the TMJ induces pain and inflammation leading to peripheral and central sensitization of trigeminal system (Villa et al., 2010). Similarly, by stimulating the TMJ with capsaicin, Thalakoti et al. (2007 found widespread peripheral sensitization in trigeminal ganglion cells. Accordingly, we hypothesized that TMJ pain might provide a suitable model to study trigeminal activation leading to DNI, as well as the mechanism of BoNT/A action in the trigeminovascular system, assumed to be involved in migraine and other headaches. In the TMJ inflammation model, apart from neurogenic plasma protein extravasation, we studied the effect of BoNT/A on CGRP, a neuropeptide considered the main mediator of trigeminal sensitization in migraine (Bigal et al., 2013).
Here, we have found that CFA‐evoked TMJ inflammation was accompanied by inflammatory changes in the cranial dura (plasma protein extravasation and inflammatory cell infiltration) and increased levels of CGRP. Additionally, following peripheral toxin injection, cleaved SNAP‐25, the product of BoNT/A enzymic activity, was colocalized with CGRP‐expressing dural afferents. BoNT/A prevented the CFA‐evoked dural inflammation and CGRP peptide increase in cranial dura.
All animal care and experimental procedures were in accordance with the 2010/63/EU Directive on the protection of animals used for scientific purposes and the recommendations of International Association for the Study of Pain (Zimmerman, 1983) and were approved by the Ethical Committee of University of Zagreb School of Medicine (permit no. 07–76/2005–43). The experimental procedures used in the work described in this article were as humane as possible. All animal studies are described in compliance with the ARRIVE guidelines for reporting experiments involving animals (Kilkenny et al., 2010).
One hundred and five male Wistar rats (average weight 300–350 g; 3–3.5 months old; University of Zagreb School of Medicine, Croatia) were used in these experiments. Rats were kept under a constant 12 h/12 h light/dark cycle with free access to food and water. The animals were randomly allocated to different experimental treatments. The experimenter conducting the behavioural testing was unaware of the tretaments given to the animals.
Animals were anesthetized with chloral hydrate (300 mg kg−1 i.p.). Injection into the TMJ was performed by inserting a 27 gauge needle medially through the skin below the inferior border of the zygomatic arch and superior to the mandibular condyl until it entered the joint capsule (Villa et al., 2010). Inflammation of the TMJ was elicited by injection of 50 μL of CFA into the left joint capsule. Control rats were injected intra‐articularly (i.a.) with saline (0.9% NaCl). Methylene blue was injected into a few animals, and the site of injection was examined in a preliminary experiment to confirm successful targeting of the TMJ.
The next day (24 h) following CFA injection, behavioural assessment of mechanical allodynia was performed using the von Frey monofilaments (Stoelting Co., Wood Dale, IL, USA) as previously described in detail (Filipović et al., 2012). Filaments produced a calibrated bending force of 0.16, 0.4, 0.6, 1, 2, 4, 6, 8 and 10. The rats were placed in a transparent plastic cage for 10 min to accommodate to the experimental environment until they assumed their normal sniffing/no locomotion position. For each session, a series of von Frey filaments were applied on the tested side of the face in ascending order, starting at 0.16 g, with three attempts until a defined behavioural response was elicited. Each time, the measurement started on the side contralateral to the CFA injection. A positive reaction was interpreted as defensive forepaw movement and/or escape/attack reaction after stimulation of whisker pad area with filaments. In total, the measurements were performed in three sessions in 10 min intervals. If no response was observed, we assigned 10 g as the withdrawal threshold, because the force exerted by thicker filaments (>10 g) was large enough to push the head of animals.
The rats were anesthetized with chloral hydrate (300 mg kg−1 i.p.) (first anaesthetic) for different BoNT/A treatments, 3 days prior to the CFA (50 μL) injection in the left TMJ (performed under the second anaesthetic). For intra‐articular injections, BoNT/A in a dose of 5 U kg−1 and 20 μL volume was injected into the left TMJ capsule of anesthetized rats, as described earlier. For intraganglionic injections,: rats were injected with BoNT/A in a dose of 2 U kg−1 (2 μL volume) into the left trigeminal ganglion of anesthetized rats, as described previously (Matak et al., 2011; Filipović et al., 2012). In brief, a Hamilton syringe needle (Hamilton Microliter #701; Hamilton, Bonaduz, Switzerland) was inserted through the skin into the infraorbital foramen and advanced through the infraorbital canal and foramen rotundum into the trigeminal ganglion.
The multiple facial injections we made as follows: anesthetized rats were injected with BoNT/A at four sites: (i) bilaterally into the rat forehead above the orbital arch and (ii) bilaterally into the whisker pad. Five microlitre Injections (5μLper site) were administered using a Hamilton syringe. A total dose of 5 U kg−1 was employed and divided in four equal doses (1.25 U kg−1 per site).
A group of animals were given sumatriptan, p.o., 24 h after CFA injection into the TMJ. The p.o. dose of 175 μg kg−1 was calculated on the basis of previously used i.v. dose (50 μg kg−1) corrected for p.o. bioavailability (25–30%) in rats (Dallas et al., 1989; Schuh‐Hofer et al., 2003). Mechanical allodynia was measured, as described above, 2 h after the administration of sumatriptan.
Plasma protein extravasation, as an indicator of neurogenic inflammation, was measured 24 h after CFA injection. This was measured by injecting Evans blue dye which complexes to plasma proteins. Anaesthetized animals were perfused transcardially with 500 mL of saline 30 min after injection of 1 mL Evans blue solution (40 mg kg−1) into the tail vein. Supratentorial dura was dissected into the left (ipsilateral to CFA treatment) and right sides (contralateral to CFA) and weighed. Evans blue was extracted in formamide, and the absorbance of Evans blue was measured spectrophotometrically. The amounts of extravasated Evans blue were calculated using the standard concentration curve, as previously described in detail (Filipović et al., 2012).
For the measurement of CGRP immunoreactivity with RIA, animals were injected with BoNT/A into the TMJ, as described above. One day after the induction of TMJ inflammation, animals were deeply anesthetized with chloral hydrate (300 mg kg−1 i.p.). Approximately 100 μL of CSF was withdrawn from cisterna magna using 27½ gauge syringe needle inserted percutaneously between the occipital bone and atlas. Only transparent CSF samples were taken for further analysis. The sample was rapidly frozen by immersing the sealed Eppendorf tube containing the CSF in liquid nitrogen and kept at −80°C. Immediately following the CSF sampling, anesthetized animals were killed by decapitation. Supratentorial dura, brainstem and trigeminal ganglion were quickly dissected, frozen in liquid nitrogen and kept at −80°C until further use. The frozen brainstem was placed in cryostat‐cooled environment (−25°C) for dissection of ipsilateral trigeminal nucleus caudalis without thawing. The nucleus was excised manually using a pre‐cooled microtome blade, scalpel and forceps. Dissected tissue was further kept at −80°C until homogenization.
Tissue samples were weighed and immediately homogenized with 1 mL distilled water and 20 μL of aprotinin solution (Trasylol, Bayer, Germany). Trigeminal ganglia and caudal nucleus samples were manually homogenized in a glass homogeniser, while dura was homogenized using a Polytron mechanical homogenizer. The samples were then centrifuged for 10 min at 8944g, and the procedure was repeated with the resulting supernatant. Final supernatants were kept at −30°C until further analysis. CSF was directly used as a RIA sample without further preparation.
Radioimmunoassay was performed similarly as previously described (Németh et al., 1998; Pozsgai et al., 2012). In brief, samples or CGRP standards (Sigma) were diluted in buffer for RIA containing 1:120 000 anti‐CGRP polyclonal antibody (Sigma) and tracer containing radio‐iodinated CGRP standard. Diluted samples were incubated at 4°C for 48 h. Antigen‐bound and free CGRP peptides were then separated by adding 100 μL of distilled water with 10% activated charcoal, 2% dextran and 0.2% fat‐free milk powder. The samples were vortexed and centrifuged at 2010g for 20 min. Levels of radioactivity of the pellets containing the free peptide and supernatant containing the antibody‐bound peptide were determined with a γ counter. Concentrations of CGRP (fmol mg−1 or fmol mL−1) in samples were calculated based on a standard concentration curve.
In order to assess inflammatory cell infiltration in the dura mater by histology, animals were injected with BoNT/A (5 U kg−1) and CFA into the TMJ as described above. One day after CFA, the anaesthetized animals were perfused with saline and 250 mL of 4% paraformaldehyde in PBS. Ipsilateral and contralateral supratentorial dura were carefully dissected and placed in paraformaldehyde fixative containing 15% sucrose, followed by 30% sucrose in PBS on the next day. After 48 h, the samples were stored at −80°C until further use.
Histological study of the cranial dural tissue was performed using standard Giemsa staining. Bright field microphotographs were taken with Olympus BX‐51 microscope coupled with DP‐70 digital camera (Olympus, Tokyo, Japan) under constant condenser light intensity and camera exposition. The number of Giemsa‐stained cell profiles was automatically quantified in four to five non‐overlapping visual fields (obtained at 20× magnification) per single animal, using cellSens Dimension programme (Olympus) as previously described in detail (Filipović et al., 2014). Five animals per group were examined.
To investigate the possible spread of peripherally injected BoNT/A to dural afferents, animals were injected in the TMJ unilaterally with 5 or 15 U kg−1 BoNT/A, as described above. One group of animals was injected with 15 U kg−1 BoNT/A into the whisker pad. An additional group of animals was injected unilaterally with a total dose of 20 U kg−1 BoNT/A (7 U per 350 g rat) divided in four injection sites (1.75 U/20 μL per site) – (i) TMJ, (ii) whisker pad, (iii) medial (forehead) and (iv) lateral (temporal) cranial region. Six days after peripheral injection of BoNT/A, animals were anesthetized and perfused for immunohistochemistry with saline and paraformaldehyde fixative.
Dural samples were stained for cleaved SNAP‐25 using the free‐floating procedure as previously described (Matak et al., 2014). In brief, dissected dura was washed in PBS, blocked with 10% normal goat serum and incubated overnight at room temperature with 1:1600 anti‐BoNT/A‐cleaved SNAP‐25 antibody (provided by Ornella Rossetto, University of Padua, Italy) in PBS containing 1% goat serum. The antibody binds specifically to BoNT/A‐cleaved SNAP‐25 and not the intact SNAP‐25 (Matak et al., 2011). Next day, the samples were incubated with Alexa Fluor 555 anti‐rabbit secondary antibody. Stained dura was carefully spread on the glass slides and cover‐slipped with an anti‐fading agent. In animals injected at four different sites or only into the TMJ (5 U kg−1), additional labelling with rabbit anti‐CGRP antibody (1:5000, Sigma) was performed. In order to prevent a possible cross‐reactivity of cleaved SNAP‐25 with CGRP, a modified primary antibody elution procedure with pre‐heated acidic buffer (50°C, pH = 2, 25 mM glycine and 1% SDS) was performed, as described previously in detail (Matak et al., 2014). After the elution, the dural samples were stained with anti‐CGRP and Alexa Fluor 488 secondary antibody. The appearance of cleaved SNAP‐25 Alexa Fluor 555 stained fibre profiles, observed before and after antibody elution, was unchanged. Cross‐reactivity controls (omitted CGRP antibody) showed no Alexa Fluor 488 signal in association with cleaved SNAP‐25 fibers, as reported previously (Matak et al., 2014).
By blocking the axonal transport within the trigeminal ganglion, we examined the involvement of the axonal traffic via the trigeminal nerve of BoNT/A for its antinociceptive activity and for the presence of cleaved SNAP‐25 in the dura mater. Anesthetized animals were injected in the TMJ with saline or BoNT/A (5 U kg−1). Immediately after TMJ injection, the animals were injected with 2 μL of saline or an equal volume of the axonal transport blocker colchicine (5 mM) into the trigeminal ganglion, percutaneously via the infraorbital canal as previously described (Filipović et al., 2012). Seven days after i.a. and i.g. treatments, the animals were treated with CFA, and the mechanical allodynia was measured after 24 h, as described above. Then, the animals were anaesthetized and perfused with saline and fixative, and the dural tissue was processed and stained for immunohistochemistry of BoNT/A‐cleaved SNAP‐25 as described above.
Results are presented as means ± SEM and analysed by one‐way ANOVA followed by the Newman–Keuls post hoc test. P < 0.05 was considered significant.
The suppliers of the reagents used were as follows: Evans blue (Merck KGaA, Darmstadt, Germany) reconstituted in 0.9% saline to obtain the required dose (40 mg kg−1); CFA cell suspension (Sigma, St. Louis, MO, USA); colchicine (Sigma, St. Louis, MO, USA); sumatriptan (Glaxo Wellcome, Taplow, UK) reconstituted in drinking water; and BoNT/A diluted in 0.9% saline (Botox®; Allergan Inc., Irvine, CA, USA). One unit (1 U) of BoNT/A preparation contains 48 pg of purified Clostridium botulinum neurotoxin type A complex.
Animals treated with CFA injected into the TMJ developed mechanical allodynia 24 h after the injection. Allodynia appeared bilaterally. Pre‐treatment with BoNT/A injected ipsilaterally to the CFA injection [both i.a. (5 U kg−1) and i.g. (2 U kg−1)] 3 days before CFA, reduced the mechanical allodynia bilaterally (P < 0.001). Similarly, 2 h after administration of sumatriptan (175 μg kg−1, p.o.), the mechanical allodynia was reduced bilaterally (P < 0.001). The differences between the BoNTA and sumatriptan treatments were not significant (Figure 1).
Dural plasma protein extravasation was significantly increased bilaterally in CFA‐injected animals compared with control values (Figures 2, ,3,3, ,4).4). Plasma protein extravasation in the ipsilateral dura was double that on the contralateral side (P < 0.001, t‐test for dependent samples). BoNT/A injected both i.a. (5 U kg−1) and i.g. (2 U kg−1), as well as sumatriptan (175 μg kg−1 p.o.), reduced the ipsilateral dural plasma protein extravasation (Figure 2). In the contralateral side, none of the treatments affected the DNI.
In a separate experiment, we employed four BoNT/A low‐dose bilateral injections into the face of the rats (Figure 4). As observed with the single BoNT/A injection into the TMJ, four injections outside of TMJ prevented both bilateral allodynia and the CFA‐evoked plasma protein extravasation (Figure 4).
Histological staining of the dural tissue of CFA‐treated rats demonstrated an elevated number of automatically counted, Giemsa‐positive, cell nuclei, compared with those in saline‐treated animals (P < 0,001), indicating an inflammatory cell infiltration. Inflammatory cells present in CFA‐injected animals (not present in saline control) were identified by an experienced pathologist, as lymphocytes, monocytes and plasma cells, as previously found in a model of trigeminal neuropathy (Filipović et al., 2014). The lack of polymorphonuclear neutrophils in dura suggests the presence of a sterile inflammation. BoNT/A prevented the increased number of Giemsa positive profiles evoked by i.a. CFA (Figure 5).
Following CFA‐induced TMJ inflammation, CGRP expression was significantly increased in dura mater and ipsilateral caudal trigeminal nuclei. BoNT/A injected into the TMJ prevented the CGRP increase in dura mater. The effect of BoNT/A on CGRP expression in trigeminal nuclei was not significant. CGRP concentration was not significantly altered in trigeminal ganglion and CSF (Figure 6).
In animals injected peripherally with BoNT/A, we observed the presence of cleaved SNAP‐25 in the injected‐side lateral and parietal dura near the dural blood vessels after BoNT/A multiple (Figure 7) and single injections into TMJ and whisker pad (not shown). Cleaved SNAP‐25 was also visible in non‐vascular areas of dura. All examined fibers containing SNAP‐25 co‐expressed bright granular immunoreactivity for CGRP (Figure 7). Contralateral dura was devoid of cleaved SNAP‐25, ruling out possible systemic BoNT/A diffusion (Figure 7). Complete colocalization of CGRP and cleaved SNAP‐25 was also visible after the single injection of BoNT/A (5 U kg−1) into the TMJ (not shown).
The anti‐nociceptive actions of BoNT/A on CFA‐induced pain was prevented by the axonal transport blocker colchicine injected into the trigeminal ganglion (Figure 8). This is in line with previous findings that BoNT/A antinociceptive activity is dependent on axonal transport (Filipović et al., 2012). Similarly, cleaved SNAP‐25 was no longer found in dura after treatment with colchicine (Figure 8). This finding suggests that, after local peripheral injection of 5 U kg−1 in the facial area, BoNT/A is axonally transported to the ipsilateral dural primary afferents by microtubule‐dependent mechanism through the ganglion.
By studying the TMJ inflammation evoked by CFA, we found that the pain in this experimental condition was accompanied by DNI. The neurogenic plasma protein leakage in cranial dural tissue was accompanied by increased inflammatory cell infiltration and up‐regulation of CGRP peptide levels (Figures 2, ,3,3, ,4,4, ,66).
Along with the present report, we have also shown that other painful stimuli in the trigeminal region (formalin‐induced or experimental neuropathic pain) were accompanied by DNI (Filipović et al., 2012, 2014). These observations demonstrate the occurrence of DNI in experimental trigeminal pain. To study migraine, other authors induced DNI more ‘artificially’ by different chemical or electrical stimuli (Markowitz et al., 1987; Buzzi and Moskowitz, 1990; O'Shaughnessy and Connor, 1994; Arulmani et al., 2006; Nelson et al., 2010; Akerman et al., 2013). Current opinion suggests that the migraine headache involves CNS dysfunction, accompanied by activation of the trigeminovascular system (Williamson and Hargreaves, 2001), and release of vasoactive peptides which induce DNI (Markowitz et al., 1987). This is not limited to experimental animals because it was clinically observed that DNI accompanies migraine and cluster headache attacks (Göbel et al., 2000; Knotkova and Pappagallo 2007). Thus, ongoing pain in the TMJ area, as well as other orofacial pain models, can be employed to study the sensitization of trigeminal dural afferents, assumed to be present in migraine and other headaches. In the present experiments, peripherally injected BoNT/A reduced mechanical allodynia and inflammatory changes in the cranial dura [plasma protein extravasation and cellular inflammatory response (Figures 1, ,2)].2)]. The similar effects of BoNT/A injections given directly into the ganglion suggests that BoNT/A action is primarily associated with the trigeminal system (Figures 1, ,22).
The recommended protocol for BoNT/A application in chronic migraine consists of multiple injections to 31 head and neck sites (Diener et al., 2010). A similar protocol is difficult to replicate in rats because of the smaller cranial dimensions. Thus, we injected BoNT/A bilaterally to the rat forehead region overlying the frontal bone (innervated by V1 ophthalmic trigeminal branch) and whisker pad (V2 maxillary branch). Such BoNT/A injections at four sites were effective in preventing CFA‐evoked pain and DNI similarly to the single BoNT/A injection into the TMJ (Figure 4). This demonstrates that the effects of BoNT/A on allodynia and DNI are not primarily mediated by its direct peripheral effect on CFA‐stimulated neurons.
Plasma protein extravasation in cranial dura is a useful marker of trigeminal activation, often employed in preclinical screening of antimigraine drugs (Markowitz et al., 1987; Buzzi and Moskowitz, 1990; O'Shaughnessy and Connor, 1994; Arulmani et al., 2006; Nelson et al., 2010; Akerman et al., 2013). DNI consists of two main components: vasodilation, which is mediated by CGRP, and plasma protein extravasation, which is mediated by substance P. Blocking only the substance P transmission by NK1 receptor antagonists did not reduce migraine symptoms, suggesting that CGRP transmission might play a more important role in the pathophysiology of migraine (Williamson and Hargreaves 2001; Peroutka, 2005). Thus, we investigated the possibility that the antimigraine actions of BoNT/A were associated with prevention of CGRP transmission. Here, we have found that peripherally injected BoNT/A prevented the CFA‐induced increase in CGRP levels in the cranial dura (Figure 6). Interestingly, in chronic migraine patients responsive to BoNT/A, the pretreatment CGRP plasma levels were increased in comparison with those in BoNT/A non‐responsive patients (Cernuda‐Morollón et al., 2014). After the treatment, BoNT/A normalized the elevated CGRP plasma levels (Cernuda‐Morollón et al., 2015). The authors posited that BoNT/A inhibits the release of CGRP from peripheral trigeminal neurons and, consequently, reduces the CGRP‐mediated trigeminal sensitization in migraine (Cernuda‐Morollón et al., 2015).
Because the anti‐migraine effect of BoNT/A is difficult to explain by its local action on peripheral, extracranial sensory nerves endings, it was suggested that BoNT/A exhibits its actions in pain and migraine by reaching dural trigeminal afferents (Matak and Lacković, 2014; Ramachandran and Yaksh, 2014). Previously, we reported that the effects of BoNT/A on trigeminal neuropathic pain and resulting DNI was prevented by colchicine injected into the ganglion, indicative of axonal transport of this toxin (Filipović et al., 2012). After BoNT/A peripheral injection, we detected cleaved SNAP‐25 in the cranial dura mater (Figures 7, ,8).8). Moreover, cleaved SNAP‐25 and CGRP were colocalized in the ipsilateral dura (Figure 7). Peripherally administered BoNT/A may prevent the SNAP‐25‐mediated release of CGRP in cranial meninges and consequent CGRP effects presumably involved in migraine pathophysiology (Williamson and Hargreaves, 2001; Durham, 2008; Geppetti et al., 2012; Karsan and Goadsby, 2015).
It was recently found that BoNT/A reduces the mechanical sensitivity of extracranially projecting collaterals of dural afferents which exit the cranium through the skull bone sutures in rats (Burstein et al., 2014). However, in our experiments, BoNT/A effects on dura mater were present even if the toxin was administered away from cranial sutures (TMJ and whisker pad). Additionally, blockade of the axonal transport of the toxin by direct i.g. colchicine prevented the formation of cleaved SNAP‐25 in the dura (Figure 8) and other effects of BoNT/A on DNI (Filipović et al., 2012). Colchicine action is limited to the injection site (Kreutzberg, 1969; Cangiano and Fried, 1977) and, therefore any possible BoNT/A axonal traffic to the dura via extracranial collaterals of dural afferents should not be prevented by administration of colchicine into the ganglion. These observations do not support an important contribution of BoNT/A local activity on extracranially projecting dural afferent collaterals.
The question arising from the present experiments is how BoNT/A crosses from the trigeminal extracranial nerves to trigeminal nerve endings in dura. Dura and extracranial trigeminal regions are innervated by separate sensory neurons (Larrier and Lee, 2003; Shimizu et al., 2012). Therefore, the transcytosis of BoNT/A from the extracranial sensory neurons to neurons that innervate dura seems the most logical explanation for the occurrence of cleaved SNAP‐25 in dura mater after facial injection of the toxin. Up to now, transcytosis of BoNT/A between different neurons has been demonstrated directly inside the retina and brain (Restani et al., 2011, 2012). In the trigeminal region, BoNT/A transcytosis within the trigeminal ganglion after its peripheral injection has been suggested by Kitamura et al. (2009. The authors investigated the effect of BoNT/A on vesicular neurotransmitter release in trigeminal neurons acutely isolated from neuropathic rats subjected to infraorbital nerve constriction injury. BoNT/A injected into the rat face induced a profound reduction of vesicular neurotransmitter release in all neurons isolated from the ganglion. They assumed that, in order to induce a widespread effect, BoNT/A was transcytosed within the ganglion (Kitamura et al., 2009). In the trigeminal ganglion, facially injected BoNT/A reduced the expression of TRPV1 channels in neurons projecting to the dura mater (Shimizu et al., 2012). These authors proposed that the effects of BoNT/A were mediated by transcytosis of the toxin, within trigeminal gangliam from extracranially projecting neurons to neurons that innervate the dura (Shimizu et al., 2012). The exact place and mechanism of such putative transcytosis remain to be elucidated. It is likely to occur within the trigeminal ganglion itself (Shimizu et al., 2012), although transcytosis in the trigeminal sensory nuclei cannot be excluded (Ramachandran and Yaksh, 2014) (Figure 9).
The conventional antimigraine drug sumatriptan, an agonist of 5‐HT1B/D receptors, reduced the pain supersensitivity and dural plasma protein extravasation in CFA‐induced TMJ inflammation, as well (Figures 1, ,2).2). Sumatriptan prevents the evoked release of CGRP and substance P in vitro and ex vivo (Buzzi and Moskowitz, 1990; Durham and Russo, 1999). Furthermore, sumatriptan reduces elevated CGRP concentrations in blood and saliva during migraine attacks (Goadsby et al., 1990; Bellamy et al., 2006). CGRP antagonists are reported to reduce the symptoms of acute migraine attacks (Edvinsson and Warfvinge, 2013). Antibodies against CGRP and CGRP receptors might also be effective as a prophylactic chronic migraine treatment (Edvinsson, 2015).
In conclusion, as demonstrated here, BoNT/A might have beneficial effect on experimental TMJ pain and the accompanying dural inflammation. The effects of BoNT/A in the cranial dura could be reconstructed as follows: after peripheral injection, BoNT/A is taken up by sensory nerve endings and axonally transported to trigeminal ganglion. After transcytosis, the toxin reaches dural nerve endings containing CGRP and suppresses the CGRP‐mediated sensitization of the trigeminovascular system and DNI. At present, this seems as the most convincing hypothesis of the action of BoNT/A in migraine and other headaches.
The work was supported by grants from Croatian Ministry of Science, Education and Sport (no. 108‐1080003‐0001 awarded to Z. L.), Croatian National Science Foundation (no. O‐1259‐2015 awarded to Z. L.), Hungarian National Brain Research Program (SROP4.2.2.A‐11/1/KONV‐2012‐0024 and the KTIA NAP_13‐1‐2013‐0001 awarded to Z. H.) and National Brain Research Program B (Chronic Pain Research Group; KTIA_NAP_13–2014‐0022; awarded to Z. L., 888819). We thank Mrs. Teréz Bagoly for her excellent technical contribution to the CGRP RIA and Prof Vladimir Trkulja for the suggestions regarding the presentation of results. Antibody to cleaved SNAP‐25 was kindly provided by Assistant Prof Ornella Rossetto (University of Padua, Italy). The histological analysis was performed by pathologist Prof Mara Dominis.
Z. L., B. F. and I. M. conceived and designed the study. Z. L., B. F., I. M. and Z. H analysed and interpreted the data. Z. L., B. F., I. M. and Z. H. drafted the manuscript. All authors have approved the final version of the manuscript. All authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.
The authors declare no conflict of interest.
Lacković Z., Filipović B., Matak I., and Helyes Z. (2016) Activity of botulinum toxin type A in cranial dura: implications for treatment of migraine and other headaches. British Journal of Pharmacology, 173: 279–291. doi: 10.1111/bph.13366.