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Nitroglycerin enhances the propagation of cortical spreading depression: comparative studies with sumatriptan and novel kynurenic acid analogues

Authors Knapp L, Szita B, Kocsis K, Vécsei L, Toldi J

Received 13 July 2016

Accepted for publication 29 September 2016

Published 20 December 2016 Volume 2017:11 Pages 27—34

DOI https://doi.org/10.2147/DDDT.S117166

Checked for plagiarism Yes

Review by Single-blind

Peer reviewer comments 3

Editor who approved publication: Professor Manfred Ogris


Levente Knapp,1 Bence Szita,1 Kitti Kocsis,1,2 László Vécsei,2,3 József Toldi1,2

1Department of Physiology, Anatomy, and Neuroscience, University of Szeged, 2MTA-SZTE Neuroscience Research Group, 3Department of Neurology, Faculty of Medicine, Albert Szent-Györgyi Clinical Centre, University of Szeged, Szeged, Hungary

Background: The complex pathophysiology of migraine is not yet clearly understood; therefore, experimental models are essential for the investigation of the processes related to migraine headache, which include cortical spreading depression (CSD) and NO donor-induced neurovascular changes. Data on the assessment of drug efficacy in these models are often limited, which prompted us to investigate a novel combined migraine model in which an effective pharmacon could be more easily identified.
Materials and methods: In vivo electrophysiological experiments were performed to investigate the effect of nitroglycerin (NTG) on CSD induced by KCl application. In addition, sumatriptan and newly synthesized neuroactive substances (analogues of the neuromodulator kynurenic acid [KYNA]) were also tested.
Results: The basic parameters of CSDs were unchanged following NTG administration; however, propagation failure was decreased compared to the controls. Sumatriptan decreased the number of CSDs, whereas propagation failure was as minimal as in the NTG group. On the other hand, both of the KYNA analogues restored the ratio of propagation to the control level.
Discussion: The ratio of propagation appeared to be the indicator of the effect of NTG. This is the first study providing direct evidence that NTG influences CSD; furthermore, we observed different effects of sumatriptan and KYNA analogues. Sumatriptan changed the generation of CSDs, whereas the analogues acted on the propagation of the waves. Our experimental design overlaps with a large spectrum of processes present in migraine pathophysiology, and it can be a useful experimental model for drug screening.

Keywords: migraine, cortical spreading depression, nitroglycerin, sumatriptan, kynurenic acid analogues

Introduction

Migraine is one of the most common neurological disorders, affecting 17% of women and 6% of men in the US.1 The environmental triggers eliciting migraine headache are diverse. The characteristic phases include aura (in a third of patients), headache, nausea, and hypersensitivity. In subgroups of patients, migraine headache is a well-managed condition; however, the therapeutic efficacy of available antimigraine drugs is in many cases limited, which necessitates unabated research efforts. The two main categories in migraine therapy include the acute and the preventive (ie, prophylactic) approaches. In acute therapy, different triptans (eg, sumatriptan) and nonsteroidal anti-inflammatory drugs are mainly used, whereas calcium-channel blockers, serotonin (ie, 5-hydroxytriptamine [5-HT]) antagonists, and β-blockers are among the drugs used for prophylaxis. Even though the research related to the processes involved in the pathomechanism of migraine has been a focus for decades, these have not yet been fully elucidated. Therefore, animal experiments are essential for further investigation of the pathophysiological processes related to migraine headache, and also for testing new substances aimed at mitigation of symptoms. The different mechanisms of migraine can be investigated from various aspects by a number of experimental models based on the sensitization or the stimulation of the trigeminal system, including the investigation of cortical spreading depression (CSD) and changes in the neurovascular system induced by NO donors.2

CSD is the electrophysiological correlate of migraine aura, and represents a potential trigger for headache.3 It is an intense self-propagating wave of depolarization involving neuronal and glial cells in the cerebral cortex, which is independent of functional areas and arterial territories.4 CSD spreads at a velocity of 3–6 mm/min and causes massive changes in ionic homeostasis. Glutamatergic mechanisms have primary roles in the propagation of CSD. Indeed, CSD cannot be induced in cases of either P/Q-type calcium channels or N-methyl-D-aspartate (NMDA) receptors being blocked in brain slices in vitro,5 or when antagonists of calcium channels or NMDA receptors are used in vivo.6,7 In addition, CSD upregulates several receptors in hippocampal and striatal territories, such as γ-aminobutyric acid A, different cholinergic (M1/2, α1/2), 5-HT serotonergic, and D1 dopaminergic, as well as NMDA-, α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid- and kainate-sensitive glutamatergic receptors.8,9 Therefore, in addition to glutamatergic mechanisms, alterations in other neurotransmitter systems participate in CSD as well. CSD also has an effect on cerebral blood flow, being associated with an initial increase in the blood flow via arteriolar dilation (mediated predominantly by NO), which subsequently turns into long-term oligemia.10,11

Experimental administration of NO donors, such as nitroglycerin (NTG), is a widely used method to model head pain. NTG elicits headache in both animals and humans.12,13 Systemic NTG administration evokes alterations in meningeal and cortical blood flow,14,15 increases the level of calcitonin gene-related peptide, and induces c-Fos expression in different brain areas associated with pain perception.16

With the use of these migraine models, several promising substances acting via various mechanisms can be investigated. The neuroactive metabolites of the kynurenine system provide a spectrum of possibilities to interfere with different neuropathological processes.17,18 Following the publication of the first studies suggesting the role of kynurenines in migraine,19 a subsequent series of research proved the beneficial effects of kynurenine-related pharmacological manipulations in migraine models.20,21 Among these substances, kynurenic acid (KYNA) has potential neuroprotective action by interfering with glutamatergic excitotoxicity. The peripheral administration of KYNA provides a number of promising results; however, these effects are limited, because of the low penetration of KYNA through the blood–brain barrier.22 Therefore, structurally modified KYNA derivates with better pharmacokinetic profiles may serve as useful tools against a large spectrum of neuropathological processes.

In this study, our aim was to investigate the effect of NTG on CSD, so as to create and validate a combined experimental migraine model, enabling the investigation of antimigraine drugs and the selection of other substances affecting the pathomechanism of migraine for further examinations. Also, we applied NTG with other molecules, including sumatriptan and novel analogues of KYNA, prior to the induction of CSD to test our combined experimental migraine model and investigate the effects of these molecules in this setting.

Materials and methods

Animals and surgery

All procedures used in this study were in accordance with the guidelines of the European Communities Council Directives (2010/63/EU) and the Hungarian Act for the Protection of Animals in Research (XXVIII.tv. 32. §). The study was approved by the National Scientific Ethical Committee on Animal Experimentation (National Competent Authority in Hungary), with the license number XX./842/2016. Male Wistar rats weighing 250–300 g were used. Animals were housed in polyethylene cages at room temperature (22°C) with a 12-hour light–dark cycle (lights on at 6 am) and free access to water and rodent laboratory chow.

All procedures were carried out under deep urethane anesthesia (1.5±0.2 g/kg body weight), as it provides very stable anesthesia in rats, lasting for several hours and being optimal for CSD recordings.23,24 During surgery and CSD recordings, the animals breathed spontaneously, and their body temperature was maintained at 37°C±0.5°C by the use of a self-regulating heating pad (TMP 5-b; Supertech Instruments, Budapest, Hungary) and a rectal probe. A trachea cannula was inserted, and heads of the animals were fixed in a stereotaxic frame. After exposure of the skull, three holes (2 mm in diameter) were drilled on the left side under cooling with saline with 3 mm between each hole (see Figure 1). Two holes were used for electrophysiological recordings above the sensorimotor cortex (bregma [Br] 1, 2 for E1, −2, 2 for E2, indicating distances in millimeters in the anterior–posterior and the medial–lateral axes from the Br, respectively). In the third hole (Br −5, 2), the dura and arachnoid mater were carefully removed, allowing access for the chemical induction of CSD. Before the recordings, the cortex was allowed to recover for 30 minutes.

Figure 1 Experimental design and representative recording from the 2-hour period following KCl administration.
Notes: On the left, filled circles indicate the exposed skull areas (1, −2, and −5 mm from the bregma in the anterior–posterior axis, respectively; 2 mm from the bregma in the medial–lateral axis). KCl (1 M) was applied at the posterior hole. Direct-current electrodes E1 and E2 were positioned at a distance of 3 mm from each other. The silver electrocorticography electrode was placed next to the E1 electrode. Vertical bars 10 mV (direct current) and 500 μV. Horizontal bar 10 minutes.

Electrophysiological recordings

Both the slow direct current (DC)-potential change and spontaneous cortical electrical activity accompanying CSD were continuously recorded for 4 hours. For the DC recordings, glass microelectrodes (1.5–2 MΩ) filled with artificial cerebrospinal fluid connected to an Ag/AgCl wire were inserted into the cortex to a depth of 800±100 μm, corresponding to cortical layer V. Electrocorticography (ECoG) was recorded from the surface of the dura with the aid of a silver electrode next to the posterior DC electrode (Br −2, 2). ECoG was recorded to monitor the depth of anesthesia and to verify the CSDs that cause a notable reduction in the ECoG amplitudes (Figure 1). In both types of recordings, common reference electrodes of the same type were placed in the masticatory muscle. DC-potential changes and ECoG were recorded by connecting the electrodes to EXP-E amplifiers (Experimetria Ltd, Budapest, Hungary).

Following offline data processing with laboratory-developed software, we examined the frequency, amplitude, time to half amplitude, velocity of propagation, and propagation failure of the CSD waves. Furthermore, we compared these parameters separately between the two recording DC electrodes (E1, E2) and between the first and second hour of recording following KCl application. The velocity of CSD-wave propagation was calculated from the time required for a CSD wave to travel the distance between the two cortical recording points. This time was measured by using the beginning of the first descending phase of the slow DC-potential change as the initial point, as previously described by Batista-de-Oliveira et al.25 DC shifts not exceeding the threshold of 5 mV were excluded from data analysis.

Experimental groups and treatments

The applied pharmacons and the saline (used as control and vehicle) were injected intraperitoneally prior to KCl administration at the given time point (Figure 2). The control group (n=6) received 2.5 mL of saline, whereas the NTG group (n=5) was treated with 10 mg/kg NTG (Nitro Pohl; G Pohl-Boskamp GmbH and Co KG, Hohenlockstedt, Germany) at minute 10. In the NTG + sumatriptan group (n=5), sumatriptan (Imigran; GlaxoSmithKline PLC, London, UK) at a dose of 0.6 mg/kg was applied 10 minutes after the NTG injection, in accordance with Bates et al.26 The KYNA analogues (SZR-105 and SZR-109; each n=5) were both administered at a dose of 0.5 mmol/kg at minute 90 (80 minutes after NTG administration, 30 minutes before CSD induction).

Figure 2 Experimental design of the different groups. Numbers represent hours of recording.
Abbreviations: NTG, nitroglycerin; CSD, cortical spreading depression; Suma, sumatriptan.

The KYNA analogues SZR-105 and SZR-109 are novel neuroactive KYNA derivatives, substituted at C3. According to preliminary studies, these molecules might be effective neuroprotective or effective compounds in certain neurological diseases (eg, in Alzheimer’s disease, Parkinson’s disease, Huntington’s disease, amyotrophic lateral sclerosis, stroke, multiple sclerosis, and migraine).

In all groups, CSD waves were continuously elicited for 2 hours from the 120th min by placing a cotton ball (diameter 1 mm) soaked with 1 M KCl solution onto the cortex through the posterior hole. To keep the cotton ball moist, it was impregnated with 5 μL of KCl solution every 15 minutes.

Statistical analysis

IBM SPSS 20 software was used for the analyses. Electrophysiological data between the two electrodes were compared separately by the use of nonparametric related-sample Friedman two-way analysis of variance (ANOVA) by rank. To analyze the differences between the groups, nonparametric independent-sample Kruskal–Wallis ANOVA was used. Data are expressed as mean and standard deviation. Differences were considered statistically significant when P≤0.05.

Results

The slow potential change in the DC-potential recordings clearly denoted the presence of CSDs after KCl stimulation, which could also be easily detected by the farther, second DC electrode (E2). In some cases, more CSDs were detected by E2, which can be attributed to a very slight depolarization of the area under E1.

After analysis of the data, the amplitude, velocity, and time to half amplitude of the CSDs showed no significant differences between the groups (Table 1). None of these parameters differed significantly when comparing the data obtained from the two electrodes separately (Table 1) or when comparing the first and the second hour (data not shown). However, a slight increase in the amplitudes was observed at E2.

Table 1 Parameters of CSD
Notes: *P=0.032 (multiple comparison of NTG groups by Kruskal–Wallis ANOVA); values are mean ± SD.
Abbreviations: CSD, cortical spreading depression; NTG, nitroglycerin; Suma, sumatriptan; ANOVA, analysis of variance; SD, standard deviation.

In the control group, we observed a constantly occurring propagation failure (20%±1%) (Figure 3A), which resulted in decreased CSD numbers recorded by E2. This tendency was observed in almost all the recordings (Figure 3A), and proved to be significant (P=0.046) based on pairwise comparison (two-way Friedman’s ANOVA). The CSD numbers (similarly to all other groups) recorded by either E1 or E2 showed no difference between the first and second hours of KCl administration (E1 9.3±4, 10.5±4; E2 8.0±3, 7.4±2) (Figure 3B).

Figure 3 CSD frequency and ratio of propagation.
Notes: (A) Number of CSDs/2 hours in all experiments and groups. The connecting lines show the data from single experiments, recorded by E1 and E2. The slope of the lines indicates the ratio of propagation, based on the different CSD number recorded by the two electrodes. In this parameter, significant differences were observed in the control group and both of the NTG + SZR groups (pairwise comparison within the groups with Friedman’s ANOVA; *P=0.046, 0.046, 0.025). (B) Average (±SD) CSD numbers in the different groups, detected by E1 and E2. Significant decrease in CSD number recorded by E2 was observed in the NTG + Suma group using multiple comparison between the groups and electrodes (Kruskal–Wallis ANOVA; +P=0.032). Horizontal lines within bars represents CSD number (mean ± SD) in the first hour. There was no significant difference between the first and second hour recorded by either of the electrodes in any groups. (C) Average (±SD) ratio of propagation in the different groups (CSDs at E2/CSDs at E1).
Abbreviations: CSD, cortical spreading depression; NTG, nitroglycerin; ANOVA, analysis of variance; SD, standard deviation; Suma, sumatriptan.

The administration of NTG slightly but insignificantly elevated CSD numbers and significantly changed the ratio of propagation (1.02±0.1). In this case, no significant difference was observed between the electrodes, as opposed to the control group (Figure 3A). In the NTG + sumatriptan group, CSD numbers decreased when sumatriptan was applied 10 minutes after NTG treatment. Significant differences were detectable in multiple comparisons of CSD numbers recorded by E2 in the different groups (Figure 3B). In this group, the ratio of propagation (1.03±0.1) was similar to that in the NTG group (Figure 3A and C).

Both of the KYNA analogues applied after NTG injection restored CSD numbers and the ratio of propagation to the control level (Figure 3). In each animal (n=5 in both KYNA analogue-treated groups), the number of CSDs at E2 was less than or at most equal with that observed at E1, which resulted in significant decreases in related-sample analyses (P=0.046 and P=0.025 for the two KYNA-analogue groups, respectively; Figure 3A and C).

Discussion

Despite the large amount of accumulated knowledge about the processes involved in migraine pathogenesis, the available treatments are at present often limited and suboptimal. Therefore, new experimental models, candidate compounds and drug targets are still the focus of antimigraine research.27,28 Cortical excitability in CSD is a physiological correlate of aura in migraine,29,30 which prompted us to investigate the hypothesis whether NTG can influence the characteristics of CSDs.

Based on a number of studies, CSD is an “all or none” phenomenon, making it difficult to detect remarkable changes in various CSD parameters following the acute administration of potential antimigraine drugs.3133 The most relevant CSD parameters include the susceptibility (examined by increasing electrical stimulation), the frequency (in cases of continuous KCl application), and the velocity of SD. Of note, the amplitude and the duration are quite constant in most experiments.34

In the present study, the progression of the depolarization wave failed between the two recording points in 20% of the CSDs, indicative of the presence of inhibitory effects in the cortical tissue under physiological conditions (notably during anesthesia). However, the propagation of the CSDs was unimpeded after the systemic administration of NTG, molecules of which may provide support against homeostatic and energetic disturbances caused by the CSDs,35 resulting in enhanced propagation. In contrast to our results, some studies have proved an inverse relationship between tissue NO level and susceptibility in human and rodent cortices36 and also in chicken retina.37 Low NO level or inhibited NOS increased tissue susceptibility to CSD. Furthermore, CSDs themselves increase NO levels,38 and thus additional NTG may contribute to the release or appearance of other NO metabolites. Further investigations are needed to identify the detailed mechanisms and to explore the active substances that take part in this phenomenon. Nevertheless, in point of fact, we suggest that the altered physiological state caused by NTG administration can be influenced more easily than the baseline parameters of CSDs; therefore, this model may provide an opportunity to test compounds with only moderate or subtle effects via the assessment of the ratio of propagation. Our results clearly demonstrate the effect of NTG administration on CSD propagation. There have been limited studies to investigate the NTG effect on CSD. Read et al confirmed that NTG causes elevated brain NO levels in anesthetized cats.39 The susceptibility, duration, and amplitude of CSDs were not changed by NTG; however, CSD-induced local NO concentration was elevated. In another study, Bates et al performed experiments on mice to investigate CSD susceptibility following NTG administration, but they did not find any differences between the groups.26 In our study, sumatriptan decreased the frequency of CSDs; however, the ratio of propagation remained similar to that seen in the NTG group. Sumatriptan has been proven to be effective in migraine by acting on the serotonin system through the activation of 5-HT1B/1D receptors. Decreased 5-HT level is closely associated with headache.40 It is known that 5-HT receptors are involved in neurogenic cranial vascular changes. Indeed, meningeal blood flow increases following the application of the 5-HT7-receptor agonist, whereas 5-HT7-receptor antagonist plus sumatriptan as a 5-HT1B/1D agonist causes decreased blood flow.41 In a prior study, sumatriptan decreased the concentration of NO following CSD induction,42 and alleviated mechanical and thermal allodynia that developed as a result of NTG administration.26 In a vessel-free preparation of chicken retina, sumatriptan blocked the SD in a concentration-dependent manner, which indicates that the effect must be related to neuronal tissue.43 Nevertheless, there is no evidence that sumatriptan can strongly modulate CSDs.44,45 In the present study, we cannot give a full explanation of the mechanisms underlying our results. However, we suggest that the 5-HT receptors directly involved in CSD could contribute to this effect.

This is the first study with these novel KYNA analogues demonstrating an effect; indeed, the elevated ratio of propagation was restored to the control level by these compounds, whereas the number of CSDs remained largely unchanged. There are several possibilities to explain these results, including the potential modulatory effect of these analogues on glutamatergic transmission by means of the inhibition of NMDA receptors, similarly to KYNA; however, further investigations are needed to be conclusive at this point. The beneficial effects of KYNA46 and its different analogues have been proven in different migraine models. The KYNA analogue SZR-72 mitigated systemic NTG-induced increase in the number of neurons expressing c-Fos47 and nNOS.48 Furthermore, SZR-72 attenuated the NTG-induced decrease of histochemical changes in the caudal trigeminal nucleus.49 The dissimilar effects of sumatriptan and KYNA analogues on CSDs suggest two inhibitory mechanisms. Further investigations are required to clarify the mechanisms underlying these effects; however, we can conclude that sumatriptan acts on the generation of the waves, whereas KYNA analogues interfere with the propagation of CSDs. Nevertheless, we cannot exclude the possibility that the analogues may counteract the effect of NTG and thereby restore normal conditions.

Conclusion

In summary, peripheral administration of NTG enhanced the propagation of CSDs. Sumatriptan, a widely used antimigraine drug, caused detectable changes in CSD frequency, which indicates the relevance of our model. Additionally, the elevated ratio of CSD propagation caused by NTG was decreased by SZR-105 and SZR-109. These results clearly show the effectiveness of these promising KYNA analogues. Here, we have presented a combined experimental migraine model for testing drugs and other pharmacological agents affecting processes involved in the pathomechanism of migraine.

Acknowledgments

This work was supported by projects OTKA KI05077 and TÁMOP-4.2.2.A-11/1/KONV-2012-0052, the European Union and the state of Hungary, cofinanced by the European Social Fund in the framework of TÁMOP 4.2.4.A/2-11-1-2012-0001 National Excellence Program, by the MTA-SZTE Neuroscience Research Group, by the Hungarian Brain Research Program (grant KTIA_13_NAP-A-III/9), by GINOP-2.3.2-15-2016-00034 and by the EUROHEADPAIN (FP7-Health 2013 Innovation, grant 602633). The authors gratefully thank Dr Levente Szalárdy for linguistic correction of the manuscript.

Disclosure

The authors report no conflicts of interest in this work.


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