No relevant modulation of TRPV1-mediated trigeminal pain by intranasal carbon dioxide in healthy humans
© Jürgens et al.; licensee Springer. 2013
Received: 13 January 2013
Accepted: 12 March 2013
Published: 10 April 2013
Nasal insufflation of CO2 has been shown to exert antinociceptive respectively antihyperalgesic effects in animal pain models using topical capsaicin with activation of TRPV1-receptor positive nociceptive neurons. Clinical benefit from CO2 inhalation in patients with craniofacial pain caused by a putative activation of TRPV1 receptor positive trigeminal neurons has also been reported. These effects are probably mediated via an activation of TRPV1 receptor - positive neurons in the nasal mucosa with subsequent central inhibitory effects (such as conditioned pain modulation). In this study, we aimed to examine the effects of intranasal CO2 on a human model of craniofacial pain elicited by nasal application of capsaicin.
In a first experiment, 48 healthy volunteers without previous craniofacial pain received intranasal capsaicin to provoke trigeminal pain elicited by activation of TRVP1 positive nociceptive neurons. Then, CO2 or air was insufflated alternatingly into the nasal cavity at a flow rate of 1 l/min for 60 sec each. In the subsequent experiment, all participants were randomized into 2 groups of 24 each and received either continuous nasal insufflation of CO2 or placebo for 18:40 min after nociceptive stimulation with intranasal capsaicin. In both experiments, pain was rated on a numerical rating scale every 60 sec.
Contrary to previous animal studies, the effects of CO2 on experimental trigeminal pain were only marginal. In the first experiment, CO2 reduced pain ratings only minimally by 5.3% compared to air if given alternatingly with significant results for the main factor GROUP (F1,47 = 4.438; p = 0.041) and the interaction term TIME*GROUP (F2.6,121.2 = 3.3; p = 0.029) in the repeated-measures ANOVA. However, these effects were abrogated after continuous insufflation of CO2 or placebo with no significant changes for the main factors or the interaction term.
Although mild modulatory effects of low-flow intranasal CO2 could be seen in this human model of TRPV-1 mediated activation of nociceptive trigeminal neurons, utility is limited as observed changes in pain ratings are clinically non-significant.
KeywordsCarbon dioxide Trigeminal pain TRPV1 Capsaicin Headache
While efficacy of high-flow oxygen has been studied in several placebo-controlled studies on cluster headache [1, 2] and recently in migraine as well [3, 4], little is known on effects of carbon dioxide (CO2) on the craniofacial nociceptive system.
Phasic nasal insufflation of CO2 is used to elicit experimental trigeminal pain in humans  to record negative mucosal potentials  and chemosensory evoked potentials . However, if given continuously, a significant habituation i.e. a decrease of CO2-induced pain can be observed after some minutes . Likewise, repeated short stimuli of CO2 with high CO2 concentrations (more than 90% v/v) induce a rapid attenuation of negative mucosal potentials . These results were translated into therapeutic utility by showing a reduction of post-dural puncture headache  and chronic cluster headache  upon prolonged inhalation of CO2. Preliminary data also show efficacy of nasal CO2 insufflation in migraine patients [11, 12].
The putative mode of action is uncertain. As CO2 is a potent vasodilator, the first studies attributed possible therapeutic effects to the vasodilating properties on cerebral vessels. More recently, CO2 has been shown to be a powerful modulator of activated nociceptive trigeminal neurons . Tzabazis and co-workers sensitized rat cheeks with capsaicin and insufflated CO2 or air nasally . Nocifensive behaviour defined as facial and hind paw withdrawal to radiant noxious heat was significantly attenuated by higher CO2 flow rates of 0.8 l/min but not of 0.4 l/min CO2 or air. Based on additional pharmacological experiments the authors concluded that CO2 exerts its antinociceptive, respectively antihyperalgesic effects by activation of mucosal primary trigeminal afferents through a decreased mucosal pH within the nasal cavity.
These findings are well in line with the hypothesis that TRPV1 receptor positive trigeminal C and A delta fibres (which are activated by application of capsaicin) may play a relevant role in the pathogenesis of primary headaches such as migraine  although this concept has been challenged recently as TRPV1 receptor blockade was inefficient in in vivo models of migraine .
How painful is prolonged intranasal application of CO2 on a numerical rating scale at a flow rate of 1 l/min?
Does intranasally applied CO2 lead to relevant systemic changes of pH and pCO2 in capillary blood samples?
Does intranasal insufflation of CO2 modulate pain ratings after intranasal application of capsaicin?
We conducted a controlled randomized parallel-group study to investigate the effects of intranasal CO2 on TRPV1-mediated trigeminal pain in healthy volunteers. All participants provided written informed consent prior to inclusion into the study. Our study was approved by the local Ethics Committee (protocol number PV3814) and conformed to the Declaration of Helsinki.
Reporting of epidemiological details for the entire cohort and the corresponding subgroups
Mean age (SEM)
24.8 years (±0.5)
25.1 years (±0.7)
t(46) = -0.636; p = 0.528
Gender ratio (male:female)
χ2(1, n = 48) = 0.000; p = 1.000
Pilot study on the effects of nasal CO2 insufflation
Experiment 1: alternating nasal application of CO2 and air after nociceptive stimulation with intranasal capsaicin
In the main study (Figure 1), 48 healthy volunteers received intranasal CO2 (1 l/min) and air (1 l/min) alternatingly. If volunteers had already participated in the pilot study, both experimental sessions were separated by at least 6 weeks. Again, subjects rated the magnitude of pain verbally on a numerical rating scale (NRS) ranging from 0 (non-painful) to 10 (worst imaginable pain).
Initially, participants received one puff of capsaicin spray (200 μg per puff, custom formulation supplied by the local pharmacy, for details see below) into the left nostril to trigger TRPV1-mediated trigeminal nociception. After three initial pain ratings on a NRS every 60 seconds (Figure 1), CO2 and air were insufflated for 60 sec each in an alternating fashion via a nasal cannula. During an interval of 20 sec between exposure to either CO2 or air, no gas was applied and the participant was asked to rate the resulting pain on a NRS. After 4 cycles, insufflation was interrupted for 1 min to allow participants to remove excessive nasal discharge. However, subjects were asked not to blow their noses to avoid early removal of the intranasal capsaicin. Thereafter, 4 identical cycles of CO2, respectively air were given and subjects were asked to rate the pain on the NRS.
Experiment 2: nasal application of CO2 or placebo after stimulation with intranasal capsaicin
In the subsequent second experiment separated from the first experiment by at least 4 weeks all participants from the first experiment were randomly allocated to receive either CO2 (1 l/min) or placebo in 2 subgroups of 24 subjects each.
Again, participants received 1 puff of capsaicin spray into the left nostril. Pain ratings on a NRS were noted every 60 sec over the entire duration of this experiment (Figure 1). After 120 sec, participants received either continuous nasal insufflation of CO2 for a total of 18:40 min via a nasal cannula or placebo (nasal cannula alone without any gas insufflation) and rated the pain on the NRS as in the pilot study.
Insufflation of CO2 and air
Medical grade CO2 (TMG, Krefeld, Germany) was administered from compressed gas cylinders with a volume of 10 l. By using a combined pressure reducing valve (200 mbar/4.5 mbar) and flowmeter (Gloor, Burgdorf, Switzerland) a constant flow of 1 l/min was maintained. Medical grade compressed air was obtained from the hospital gas reticulation system and delivered at a flow of 1 l/min by a flow meter (Dräger, Lübeck, Germany). Nasal cannulae (Dahlhausen, Köln, Germany) were used to apply both gases locally into both nasal cavities.
As CO2 should only be insufflated nasally and not inhaled due to safety concerns, all subjects were trained before the first experiment. CO2 was applied bilaterally into the anterior nasal cavity, where highest mucosal responsiveness of evoked potentials to short pulses of CO2 could be found , namely at the anterior septum as compared to more posterior parts. They were instructed to breathe-in through the mouth und exhale through the nose. Before each experiment they were reminded to adhere to these instructions.
TRPV1 activation with capsaicin
One puff of a nasal spray containing 200 μg of capsaicin (prepared from 1.42 ml capsaicin liquid extract in 10 ml of refined sesame oil) was applied to the left nostril with the head in a stooped position to avoid contamination of the pharynx. Participants were allowed to remove excessive nasal discharge by soaking cotton swaps, but were asked not to blow their noses to avoid early removal of intranasal capsaicin.
Capillary blood gas analysis
Blood gas analyses were collected in from the earlobe in capillary tubes after pretreatment with an ointment containing 5% benzyl nicotinate (supplied by the hospital pharmacy) for 10 mins. Immediately afterwards samples were tested with a blood gas analyzer (ABL5, Radiometer Medical, Brønshøj, Denmark). The manufacturer’s reference values for capillary blood gas analysis were as follows: pH 7.35- 7.45; pCO2 males: 35-48, females: 32-45.
Data evaluation and statistics
Descriptive statistics are given as mean values and standard errors of the mean. Differences on mean values were either examined by paired t-tests or by means of a repeated measures analysis of variance (ANOVA). For analysis of pain ratings over time in the pilot study, the factor TIME (pain ratings 1-15) was used, for other comparisons of pain ratings a two-way repeated measures ANOVA with the factors TIME (corresponding pain ratings) and GROUP (CO2 or air). Comparison of categorical data (gender) was done by means of the chi square test. In all tests p values <0.05 were considered significant.
Bivariate correlations were calculated by Pearson’s correlation analysis with p < 0.05 regarded as significant. All analyses were done with SPSS 20 (IBM, Amonk, NY, USA).
Nociceptive properties of intranasal CO2
If subjects accidentally inhaled CO2 nasally or started talking during the training phase, they mostly complained of a highly unpleasant irritation spreading from the nasal cavity into the nasal sinus and the pharynx which led to interruption of the training.
Net changes of pCO2 levels (difference between pCO2 after – pCO2 before insufflation) did not correlate with corresponding pain ratings in the pilot study (Pearson’s bivariate correlation: p > 0.05).
Modulatory effects of alternating insufflation of CO2and air on TRPV1-mediated nociceptive trigeminal activation
For epidemiological details see Table 1. Mean values for all pain ratings after insufflation of CO2 (3.6 ± 0.3) and air (3.8 ± 0.3) respectively differed significantly (t(47) = -2.107; p = 0.041). Likewise, a repeated-measures ANOVA for the factors TIME (pain ratings for insufflation 1 to 4) and GROUP (CO2 or air) yielded no significant main effect for TIME (F1.3,63.3 = 2.039; p = 0.153), but significant results for both the main factor GROUP (F1,47 = 4.438; p = 0.041) and the interaction term TIME*GROUP (F2.6,121.2 = 3.3; p = 0.029). Mean values are given in Figure 3.
Modulatory effects of continuous insufflation of CO2or air on TRPV1-mediated nociceptive trigeminal activation
Age and gender distribution did not differ significantly between the randomly assigned subgroups receiving either CO2 or air in experiment 2 (for further details see Table 1). Mean values for each pain rating are given in Figure 4.
A repeated-measures ANOVA with the factors TIME (pain ratings 1 to 17) and GROUP (CO2 or air) yielded a significant main effect for TIME (F2.1, 98.4 = 20.119; p < 0.001), but not for the factor GROUP (F1,46) = 0.089; p = 0.767) or the interaction term TIME*GROUP (F2.1, 98.4 = 0.624; p = 0.548).
There was no baseline difference defined as comparison of the first pain rating between the CO2 and the air group after administration of capsaicin and before the first insufflation (CO2: 1.0 ± 0.4; air: 1.1 ± 0.3; t(46) = 0.15; p = 0.902).
Side effects of treatment
Reporting of safety data for 10 patients taking part in to pilot study and the corresponding statistical tests (paired t-tests, considered significant with p < 0.05)
Before CO 2insufflation
After CO 2
t(9) = 3.21; p = 0.011
t(9) = -3.15; p = 0.012
Contrary to previous animal studies, the effects of intranasally insufflated CO2 on experimental trigeminal pain were marginal. Application of CO2 alone resulted in mild pain and a significant but clinically irrelevant change in capillary pCO2 and pH levels. After nociceptive stimulation of the first trigeminal branch with intranasal capsaicin (as a model of TRPV1-mediated craniofacial pain with central sensitization), alternating application of CO2 reduced pain ratings only minimally compared to a sham paradigm with air, but this effect was abrogated during continuous insufflation of CO2.
Intranasal application of capsaicin as a human model of trigeminal nociceptive activation
Capsaicin (8-Methyl-N-vanillyl-trans-6-nonenamide) increases release of substance P and simultaneously blocks its reuptake exerting its effects by activation of the TRPV1 receptor . This leads to an activation of the trigemino-vascular system with enlargement of the internal carotid artery  if applied intracutaneously into the skin innervated by the ophthalmic division (V1) of the trigeminal nerve but not when applied to the skin innervated by the mandibular (V3) branch or the forearm. The nasal mucosa is innervated by branches of the ethmoidal (V1) and the maxillary (V2) nerve  with neurons containing predominantly substance P and - to a much lesser extent - CGRP . Noxious stimulation with capsaicin applied to the nostril causes long-lasting discharges of afferent nerve fibres of the ethmoidal nerve in guinea pigs . In another study also in guinea pigs, expression of the immediate-early gene c-fos after intranasal capsaicin was highest in the trigeminal complex with the subnuclei caudalis and interpolaris . Interestingly, the majority of cells which innervate the dura show a co-localisation of TRPV1 receptors and CGRP [24, 25].
It has been shown in in vitro experiments with slices of rat trigeminal nucleus caudalis  that activation of TRPV1 receptors on nociceptive trigeminal afferents causes release of CGRP. CGRP itself does not activate meningeal afferents but is thought to facilitate nociceptive transmission in the spinal trigeminal nucleus via presynaptic modulation of other primary afferents rather than direct effects on second-order neurons in the spinal trigeminal nucleus [27, 28]. A relevant role in migraine pathophysiology is supported by the observation that migraine attacks can be aborted by administration of CGRP receptor antagonists [29, 30]. According to Lambert and colleagues the TRPV1 receptor antagonist SB-705498 does not suppress activation in the trigeminal nucleus caudalis in cats following electrical and mechanical stimulation of nociceptive meningeal and facial afferents. However, sensitisation induced by inflammatory soup was significantly attenuated by SB-705498 . In contrast, Summ and co-workers challenged a relevant role of TRPV1 receptors in migraine pathophysiology as blockade of TRPV1 receptors did neither modulate experimentally induced cortical spreading depression nor neurogenic dural vasodilation or nociceptive transmission in the trigemino-cervical complex in rats .
Regardless of whether TRPV1 receptor positive V1 neurons are indeed involved in migraine pathophysiology or not, they have been associated with other craniofacial pain syndromes such as dental pain where an upregulation of TRPV1 expression in rat trigeminal ganglia was observed in a model of lipopolysaccharide-induced pulpitis . We note that we did not strive for a specific model such as migraine headache but a robust model of craniofacial pain including TRPV1 activation affecting the first trigeminal branch. In our sample, participants showed a transient and significant increase in pain ratings after nasal application of capsaicin which is in line with other studies showing a subsequent and temporary regional sensitization [14, 33]. Pain ratings peaked after 8-9 min which is congruent with an animal study on neuronal activity in the rat nucleus caudalis . After application of capsaicin to the eye and the tongue a delayed activity peaking also after 4-6 min was found. Thus, intranasal application of 200 μg capsaicin is a potent model for stimulation of TRPV1 positive nociceptive neurons of the first trigeminal branch.
Characteristics, tolerability and safety of intranasal insufflation of CO2
CO2 insufflation was rated as mildly painful by 65% of patients. We found systemic changes in capillary pH and pCO2 levels but no relevant alterations beyond the normative range and conclude that nasal application at 1 l/min is safe. Insufficient delivery of CO2 into the nasal cavity seems unlikely as changes of pCO2 levels after nasal insufflation did not correlate with pain ratings in our pilot study.
Our attempts to mimic CO2 induced unpleasantness respectively pain with vaporized ammonia to establish a robust sham condition were in vain (data not shown). Ammonia induced a more stabbing and - at higher concentrations - unbearable pain in the nasal cavity with variable pain thresholds. The unpleasantness of intranasal CO2 in our sample implies that true blinding is not feasible at flow rates of 1 l/min and above as most patients will notice an unpleasant or painful perception. As clinical effects were negligible in our sample, potential sources of bias such as a relevant placebo effect are unlikely.
At lower intranasal flow rates of 0.6 l/min, blinding seemed to be less problematic in prior studies. Casale et al.  reported that 80% of patients with seasonal allergic rhinitis did not notice nasal stinging or burning during nasal insufflation of CO2 at 0.6 l/min for only 1 minute – similar to the setup used in the therapeutic studies in migraine patients by Spierings [11, 12]. Inhalation of CO2 was less well tolerated raising doubts about effective blinding in prior studies reporting efficacy of inhaled CO2.
Modulatory effects of CO2 insufflation on nociceptive trigeminal activation
The antihyperalgesic efficacy of CO2 in our study was small and reached statistical significance only when CO2 and placebo were given in an alternating fashion within the same subject (experiment 1) – as opposed to application of either CO2 or air only in experiment 2. It may be easier for the participants to sense a subtle analgesic or anti-hyperalgesic efficacy of CO2 if it is given in a contrasting fashion with air as placebo.
As shown by Tzabazis and colleagues in a rat model , nasal insufflation of CO2 with flow rates of 0.8 l/min attenuated nocifensive behaviour after sensitization with capsaicin unlike lower flow rates of CO2 (0.4 l/min) or air. In the nasal mucosa CO2 decomposes into protons and carbonate catalyzed by mucosal carbonic anhydrase and activates TRPV1- and ASIC- positive neurons by proton accumulation. Subsequent, central inhibitory effects are proposed such as a widespread inhibition of afferent trigeminal input though inhibitory interneurons, trans-segmental inhibitory control circuits or conditioned pain modulation.
Vause and colleagues showed that incubation of cultured trigeminal ganglions with CO2 or capsaicin resulted in an acidification of culture medium and a consecutive nociceptive activation with CGRP release . Similarly, CO2 attenuated CGRP release by pretreatment with capsaicin if cultured under isohydric conditions which prevents extracellular but allows intracellular acidification.
Tzabazis and co-workers observed less intense and only short-lived antinociceptive or antihyperalgesic effects of CO2 insufflation on non-sensitized skin as compared to air insufflation . These findings strongly argue in favour of activity-dependent effects of CO2, so that efficacy could have been better in patients with chronic craniofacial pain. Alternatively, CO2 inhalation with a potentially different locus of action could represent a more powerful alternative although tolerability seems to limit feasibility [9, 10].
In summary, intranasal insufflation of CO2 exerts antihyperalgesic effects in animal models but resulted in only minor clinical effects in our human model of trigeminal pain elicited by activation of nociceptive TRPV1 receptors in healthy volunteers. These moderate effects question the clinical utility of intranasal CO2 in TRPV1-mediated pain at flow rates of 1 l/min.
Clinical efficacy of CO2
Marcussen and Wolff successfully treated aura symptoms in migraine patients termed as “vasoconstrictor symptoms” by inhalation of 10% CO2 in either air or oxygen for 5 min . Likewise, Sikh and Agarwal exposed 40 patients with post-dural puncture headache to 5.6% CO2 mixed with oxygen for 10 min daily which was repeated up to 2 times if the headache was not relieved . After 3 days, 98% of the patients reported relief compared to 58% of the oxygen only control group. Despite these impressive clinical results on primary and secondary headaches, patients inhaled much higher concentrations of CO2 suggesting a potentially different mode of action. In addition, translating these clinical results to our human model is difficult as the role of the TRPV1 receptor in migraine pathophysiology has been challenged . Furthermore, some studies yielded contrasting results. Engel reported that inhalation of 10% CO2 provoked a headache attack or increased headache intensity in 18 of 40 subjects with mainly posttraumatic headache and migraine. CO2-induced headache attacks or aggravation were less intense than headaches triggered by histamine and adrenaline . Likewise, Hannerz and Jogestrand reported that ipsilateral pain could be elicited in patients with active episodic cluster headache during inhalation of 6% CO2 for 6 min .
At present, a firm conclusion on the clinical efficacy of CO2 in primary and secondary headaches is difficult despite promising data from animal experiments. Trials on the efficacy of inhaled CO2 in various headache syndromes are relatively old and yielded ambiguous results. Evidence for the efficacy of intranasal CO2 in migraine has been published in preliminary form.
Only mild modulatory effects of intranasal insufflation of CO2 at flow rates of 1 l/min could be seen in a human model of TRPV1 mediated activation of nociceptive trigeminal neurons which is in line with previous studies. While application was safe, clinical utility at low flow rates was limited in our model as the therapy is uncomfortable and changes in pain ratings are therapeutically irrelevant.
The authors thank Sonja Schollmeyer for help with the arterial blood gas analyses.
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