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Dr Leonardo Resstel, Department of Pharmacology, School of Medicine of Ribeirão Preto, USP, Av. Bandeirantes 3900, 14049-900, Ribeirão Preto, São Paulo, Brazil. E-mail: firstname.lastname@example.org
Background and purpose: Cannabidiol (CBD) is a non-psychotomimetic compound from Cannabis sativa which induces anxiolytic- and antipsychotic-like effects in rodents. These effects could be mediated by facilitation of the endocannabinoid system or by the activation of 5-HT1A receptors. As either of these mechanisms could promote adaptation to inescapable stress, the aim of the present work was to test the hypothesis that CBD would attenuate the autonomic and behavioural consequences of restraint stress (RS). We also investigated if the responses to CBD depended on activation of 5-HT1A receptors.
Experimental approach: Male Wistar rats received i.p. injections of vehicle or CBD (1, 10 or 20 mg kg−1) and 30 min later were submitted to 60 min of restraint where their cardiovascular responses were recorded. The protocol of the second experiment was similar to the first one except that animals received i.p. injections of the 5-HT1A receptor antagonist WAY100635 (0.1 mg kg−1) before CBD treatment and exposure to restraint. 24 h later they were also tested in the elevated plus-maze (EPM), an animal model of anxiety.
Key results: Exposure to RS increased blood pressure and heart rate and induced an anxiogenic response in the EPM 24 h later. These effects were attenuated by CBD. WAY100635 by itself did not change the cardiovascular and anxiogenic response to RS, but blocked the effects of CBD.
Conclusion and implications: The results suggest that CBD can attenuate acute autonomic responses to stress and its delayed emotional consequences by facilitating 5-HT1A receptor-mediated neurotransmission.
The Institution's Animal Ethics Committee approved housing conditions and experimental procedures for animals. Male Wistar rats weighing 230–250 g were used. The animals were provided by our local Animal farm facility. After arriving at the Animal Care Unit of the Department of Pharmacology, School of Medicine of Ribeirão Preto, University of Sao Paulo, the animals were kept in groups of four per cage for 48 h. After this adaptation period they are housed individually in plastic cages with free access to food and water under a 12 h light/dark cycle (lights on at 06:30 h) for a further 24 h period before being subjected to the surgical procedure (see below).
Twenty-four hours before being submitted to restraint stress, animals had a polyethylene catheter implanted into the femoral artery under anaesthesia (tribromoethanol, 250 mg kg−1 i.p.), for the recording of arterial blood pressure and HR. The catheter was exposed on the dorsum of the animals and attached to the skin, allowing arterial pressure recordings from conscious animals.
Experiment 1 In the morning period (between 7 a.m. and 12 a.m.), the animals were transferred to the experimental room in their home box. Mean arterial pressure (MAP) and HR were recorded using an HP-7754A amplifier (Hewlett Packard, Palo Alto, CA, USA) connected to a signal acquisition board (Biopac M-100, Goleta, CA, USA) and computer processed. After a few minutes of baseline recording, rats received a single i.p. injection of one of the following drugs: vehicle or CBD (1, 10 or 20 mg kg−1). Thirty minutes later they were submitted to a 60 min restraint period in a small plastic cylindrical restraining tube (diameter = 6.5 cm and length = 15 cm). After the restraint period the animals returned to their cages. Each animal was submitted to only one session of restraint to prevent the development of stress tolerance (Guimaraes et al., 1993).
Experiment 2 Based on the results obtained in the first experiment, we chose the dose of 10 mg kg−1 of CBD to use in this second study. The protocol was similar to the first experiment except that before the restraint period the animals received, first, an i.p. injection of vehicle or WAY (0.1 mg kg−1) followed, 30 min later, by a second injection of vehicle or CBD (10 mg kg−1). As in experiment 1, 30 min after the last injection the animals were restrained for 60 min. One day later they were tested in the EPM. We also had a general control group of unrestrained animals treated with the saline+CBD vehicle that were tested 24 h later in the EPM.
The EPM test
The EPM test was conducted as described before (Padovan and Guimaraes, 2000). Briefly, the apparatus consisted of two opposite open arms (50 × 10 cm) crossed at a right angle by two arms of the same dimensions enclosed by 40 cm high walls with no roof. The maze was located 50 cm above the floor. Rodents naturally avoid the open arms of the EPM and anxiolytic compounds typically increase the exploration of these arms without changing the number of enclosed-arm entries (Pellow et al., 1985; Carobrez and Bertoglio, 2005). The EPM was cleaned and dried before each session and the Ethovision software (Version 1.9, Noldus, Netherlands) was employed for behavioural analysis.
Mean arterial pressure and HR values were continuously recorded for 10 min before the 60 min restraint stress period. Data were expressed as means ± SEM of MAP or HR changes (respectively Δ MAP and Δ HR) sampled at 5 min intervals. Points sampled during the 10 min before restraint were used as control baseline value. MAP and HR changes were analysed using two-way anova with treatment as independent factor and time as repeated measurement factor. When interaction between the factors was observed, groups were compared using one-way anova followed by Bonferroni's post hoc test.
The per cent of entries (100 × open/total entries) and time spent in the open arms (100 × open/open + enclosed) of the EPM were calculated for each rat. These data, together with the number of enclosed arm entries, were analysed by one-way anova followed by Bonferroni's post hoc test. Values of P < 0.05 were taken as showing statistically significant differences between means.
The following drugs were used: CBD (THC Pharma, Frankfurt, Germany): 1, 10 or 20 mg kg−1, suspended in polyoxyethylenesorbitan monooleate (Tween 80) 2%-saline (Resstel et al., 2006), WAY100635 (WAY, Sigma, St. Louis, MO, USA): 0.1 mg kg−1 dissolved in saline (Kaster et al., 2005) and tribromoethanol (Aldrich, St. Louis, MO, USA). The solutions were prepared immediately before use and injected intraperitoneally in a volume of 1 mL kg−1. The appropriate vehicles were used in each experiment.
Effects of CBD on cardiovascular responses to acute restraint Systemic injection of CBD (1, 10 and 20 mg kg−1) did not affect baseline blood pressure (F4,25 = 1.2, P > 0.05) or HR (F4,25 = 0.9, P > 0.05) values when compared with vehicle control (n = 6, Table 1). As represented in Figure 1, acute restraint induced a marked and sustained increase of HR and MAP during the 60 min test. There were significant effects of treatment (MAP: F3,240 = 93.5, P < 0.001; HR: F3,240 = 123, P < 0.001), time (MAP: F14,240 = 83.6, P < 0.001; HR: F14,240 = 27.9, P < 0.001) and treatment versus time interaction (MAP: F42,240 = 5.1, P < 0.01; HR: F42,240 = 7.9, P < 0.01).
Table 1. Basal values of the MAP and HR in vehicle (control), CBD and WAY100635 treated rats
The values in the table represent the means ± SE. One-way anova.
CBD, cannabidiol; HR, heart rate; MAP, mean arterial pressure.
n = 6
105 ± 2
338 ± 13
CBD 1 mg
n = 5
103 ± 3
363 ± 14
CBD 10 mg
n = 5
100 ± 3
349 ± 11
CBD 20 mg
n = 5
97 ± 3
369 ± 9
n = 5
99 ± 2
371 ± 14
F4,25 = 1.5, P > 0.05
F4,25 = 1.3, P > 0.05
Cannabidiol decreased the stress-induced cardiovascular responses at doses of 10 and 20 mg kg−1 (HR, F3,16 = 19.9, P < 0.001, MAP, F3,16 = 14.6, P < 0.001). The dose of 1 mg kg−1 was also able to attenuate HR responses (P < 0.05). A dose-dependency was demonstrated by nonlinear regression analysis and showed a significant correlation between doses and attenuation of the increased MAP (r2 = 0.82, df = 13, P < 0.01) and HR (r2 = 0.73, df = 13, P < 0.01) (Fig. 2).
Effects of WAY100635 on CBD effects on acute cardiovascular responses to restraint WAY (n = 5) did not affect baseline values of blood pressure (F4,25 = 1.2, P > 0.05) or HR (F4,25 = 0.9, P > 0.05) compared with CBD (10 mg kg−1, n = 6) and vehicle (n = 6, Table 1).
There were significant effects of restraint (MAP: F3,270 = 35.95, P < 0.001; HR: F3,270 = 104.3, P < 0.001), time (MAP: F14,270 = 59.66, P < 0.001; HR: F14,270 = 66.4, P < 0.001) and treatment versus time interaction (MAP: F42,270 = 2.1, P < 0.01; HR: F42,270 = 1.9, P < 0.01) (Fig. 3).
The decrease of the cardiovascular responses by systemic administration of CBD (10 mg kg−1) was prevented by WAY (MAP: F1,135 = 139.5, P < 0.001; HR: F1,135 = 290.3, P < 0.001) (Fig. 3). The latter drug, by itself, had no effect on cardiovascular responses to restraint (MAP: F1,135 = 1.3, P > 0.05; HR: F1,135 = 1.1, P > 0.05) (Fig. 3).
Typical experimental recordings showing the effects of CBD and WAY on cardiovascular responses observed during acute restraint can be seen in Figure 4.
Effects of CBD and WAY100635 on delayed behavioural consequences in the EPM induced by restraint Acute restraint induced a significant decrease in the percentage of open arm entries (F3,25 = 7.72, P < 0.001) compared with unrestrained controls (n = 6), when tested 24 h after stress (Fig. 5). CBD administration in restrained rats (n = 6) increased the percentage of open arm entries (P < 0.001, Fig. 5) compared with controls (vehicle-treated restrained animals, n = 6). This effect was prevented by pre-administration of WAY (P < 0.001, n = 6). No effect was found in animals treated only with WAY (P > 0.05, n = 6) (Fig. 5). There was also no effect on the percentage time spent in the open arms and in the number of enclosed arm entries (P > 0.05).
The present results showed that (i) CBD reduced the pressor and tachycardic responses to restraint stress, in a dose-dependent manner; (ii) CBD attenuated the increased anxiety behaviour caused by a previous exposure to restraint; and (iii) effects of CBD on cardiovascular and behavioural responses to restraint can be blocked by WAY100635, a 5-HT1A receptor antagonist.
Cannabidiol did not induce any significant change in basal MAP and HR which agrees with the reported lack of significant cardiovascular effects of this drug (McQueen et al., 2004; Resstel et al., 2006). At low doses, it also does not interfere with memory and learning processes (Lichtman et al., 1995; Fadda et al., 2004; 2006). It is unlikely, therefore, that the attenuation of the cardiovascular and delayed behavioural responses to restraint depend on direct cardiovascular effects or memory impairment induced by the drug, but rather on an attenuation of the emotional response to stress. In agreement with this proposal, acute administration of CBD has been shown to induce anxiolytic-like effects in several animal models, including the EPM, Vogel conflict test and contextual fear conditioning (Guimaraes et al., 1990; Onaivi et al., 1990; Moreira et al., 2006; Resstel et al., 2006). The effective doses of CBD in these previous studies were, in general, similar to ours. In the study by Guimaraes et al. (1990), however, CBD produced an inverted U-shaped dose-response curve, with the highest dose (20 mg kg−1) being ineffective. The reasons for this difference are unknown, but may depend on the model used (Calabrese, 2008). As the EPM test is based on exploratory activity, it could be more prone to interference of non-specific drug effects that affects this parameter (Calabrese, 2008). In addition, at least for classical anxiolytics such as diazepam, the EPM is more sensitive than other models such as the Vogel conflict test (see Calabrese, 2008).
The mechanisms of the anxiolytic and anti-stress effects of CBD are not clear. It has a low affinity for cannabinoid receptors (Petitet et al., 1998; Thomas et al., 1998) although, under certain circumstances, it may act as an antagonist of CB1- and CB2-receptor agonists (Pertwee et al., 2002). CBD could also block the reuptake and metabolism of anandamide, facilitating endocannabinoid-mediated neurotransmission (Watanabe et al., 1998; Di Marzo et al., 1999; Bisogno et al., 2001; Mechoulam et al., 2002). However, several effects of CBD have been shown to be independent of the endocannabinoid system (Hayakawa et al., 2007). More recently, Russo et al. (2005) reported that CBD can displace the 5-HT agonist [3H]8-OH-DPAT from cloned human 5-HT1A receptors expressed in Chinese hamster ovary cultured cells. Moreover, using signal transduction studies, this work also showed that CBD can act as an agonist at these receptors. The observation that CBD has agonistic properties at 5-HT1A receptors has been supported by in vivo studies where the neuroprotective and anti-oxidative effects induced by CBD were blocked by pre-treatment with the 5-HT1A antagonist WAY100135 (Mishima et al., 2005; Hayakawa et al., 2007). Our results corroborate these findings, by showing that the stress-attenuating effects induced by CBD were prevented by systemic pretreatment with WAY100635, a selective antagonist at these receptors. In agreement with our results, a recent study from our laboratory showed that CBD interacts with 5-HT1A receptors in the dorsolateral periaqueductal gray to produce anxiolytic-like effects in the EPM (Campos and Guimaraes, 2008).
5-HT1A receptors are widely distributed in the brain, especially in structures traditionally related to stress and anxiety, such as the raphé nuclei, hippocampus, prefrontal cortex, amygdala and hypothalamus (Chalmers and Watson, 1991). Although the role of 5-HT in anxiety is still a matter of intense debate (Millan, 2003), several pieces of evidence suggest that activation of 5-HT1A receptors facilitates adaptation to stress (Kostowski et al., 1992; Dekeyne et al., 2000; Tsuji et al., 2000; Blier and Ward, 2003; Joca et al., 2003; Kagamiishi et al., 2003; Rioja et al., 2004; Joca et al., 2007). For example, pre-administration of a 5-HT1A agonist before an acute immobilization period blocked the stress-induced anxiogenic effect observed in an elevated T-maze test performed 24 h later (Rioja et al., 2004). Similar results were reported by Tsuji et al. (2000), who observed that administration of 5-HT1A receptor agonists before restraint stress attenuated, in a dose-dependent manner, the development of stress-induced anxiogenic effect observed 24 h later in the hole-board test of anxiety. Data from 5-HT1A receptor knockout mice give further support to this hypothesis, as these animals display anxiogenic-like behaviour in different paradigms (Zhuang et al., 1999; Tsetsenis et al., 2007). It is proposed that the lack of this receptor would promote a bias in the processing of threatening cues which could render the animal more susceptible to the development of behavioural consequences of stress (Tsetsenis et al., 2007). On the other hand, facilitation of this neurotransmission would mediate adaptation to stress (Graeff et al., 1996). This suggestion is supported by results showing that behavioural adaptation to stress is accompanied by sensitization of 5-HT1A-mediated neurotransmission (Kennett et al., 1985b; 1987; Samad and Haleem, 2007) and that an increased expression of this receptor in the brain is associated with reduced anxiety-like behaviour (Kusserow et al., 2004). Therefore, these studies support the possibility that activation of 5-HT1A receptors protects animals against various emotional changes caused by stressful stimuli, perhaps by facilitating mechanisms involved in the ability to cope with the stressful situation.
The exact mechanism through which 5-HT1A agonists induce their anxiolytic activity remains unclear. 5-HT1A receptors are located presynaptically (somatodendritic autoreceptors) in 5-hydroxytryptaminergic cell bodies in the raphé nuclei of the brain stem and postsynaptically, predominantly in limbic structures such as the hippocampus and the hypothalamus (Verge et al., 1985; 1986; Chalmers and Watson, 1991). It is still controversial whether the anxiolytic-like effects induced by acute systemic administration of 5-HT1A agonists are due to the activation of the pre- or the post-synaptic receptors (File et al., 1996; Lopez-Rubalcava, 1996). Moreover, depending on the structure where post-synaptic 5-HT1A receptors are located, their activation may lead to anxiolytic or anxiogenic-like effects (Graeff et al., 1996; Zangrossi et al., 2001). Therefore, the exact mechanism of action of 5-HT1A agonists as anxiolytic compounds is complex and still warrants further investigation.
In conclusion, the present findings indicate that CBD, by activating 5-HT1A receptors, can attenuate physiological and behavioural responses to restraint stress. This finding raises the possibility that CBD could be useful for treating psychiatric disorders thought to involve impairment of stress-coping mechanisms, such as depression and post-traumatic stress disorder.
The authors wish to thank Ivanilda A.C. Fortunato and José Carlos A. for technical help. The present research was supported by grants from CNPq and FAPESP.