Research Article | Open Access
Luciano L. Furlanetti, Máté D. Döbrössy, Iñigo A. Aranda, Volker A. Coenen, "Feasibility and Safety of Continuous and Chronic Bilateral Deep Brain Stimulation of the Medial Forebrain Bundle in the Naïve Sprague-Dawley Rat", Behavioural Neurology, vol. 2015, Article ID 256196, 13 pages, 2015. https://doi.org/10.1155/2015/256196
Feasibility and Safety of Continuous and Chronic Bilateral Deep Brain Stimulation of the Medial Forebrain Bundle in the Naïve Sprague-Dawley Rat
Objective. Deep brain stimulation (DBS) of the superolateral branch of the medial forebrain bundle (MFB) has provided rapid and dramatic reduction of depressive symptoms in a clinical trial. Early intracranial self-stimulation experiments of the MFB suggested detrimental side effects on the animals’ health; therefore, the current study looked at the viability of chronic and continuous MFB-DBS in rodents, with particular attention given to welfare issues and identification of stimulated pathways. Methods. Sprague-Dawley female rats were submitted to stereotactic microelectrode implantation into the MFB. Chronic continuous DBS was applied for 3–6 weeks. Welfare monitoring and behavior changes were assessed. Postmortem histological analysis of c-fos protein expression was carried out. Results. MFB-DBS resulted in mild and temporary weight loss in the animals, which was regained even with continuing stimulation. MFB-DBS led to increased and long-lasting c-fos expression in target regions of the mesolimbic/mesocortical system. Conclusions. Bilateral continuous chronic MFB-DBS is feasible, safe, and without impact on the rodent’s health. MFB-DBS results in temporary increase in exploration, which could explain the initial weight loss, and does not produce any apparent behavioral abnormalities. This platform represents a powerful tool for further preclinical investigation of the MFB stimulation in the treatment of depression.
Major depressive disorder (MDD) is a debilitating predicament with negative consequences on both the affected individual and those close to the suffering person. Today, the best therapies include psychotherapy, electroconvulsive, and drug treatment ones, together producing remission in 70–90% of sufferers; however, 10–30% of the patients remain resistant to all currently available treatment combinations. Deep brain stimulation (DBS), considered in the past uniquely in the context of motor symptoms observed in essential tremor, Parkinson’s disease, and dystonia, has since 2005 also been tested in MDD [1–4]. The limited number of clinical studies targeting treatment-resistant MDD by DBS ranges from a case study  to small trials [6–9] and suggests that the approach both is safe and can show long-lasting efficacy in a significant number of patients who have not responded positively to other types of interventions. The stimulation targets selected in these clinical studies included the subcallosal cingulate, nucleus accumbens (NAC), and the habenula. The diversity of targets reflects the characteristics of the network-model of depression that states that aspects of the syndrome (e.g., cognitive, vegetative, and somatic) can arise from dysregulation of neuronal activity at numerous loci on the limbic-cortical circuitry [7, 10].
A recent clinical trial in treatment-resistant MDD patients stimulated bilaterally the superolateral branch of the medial forebrain bundle (slMFB) [9, 11]: a brain structure upstream from all previous targeted areas, and thereby potentially affecting their neural activity. The stimulation of these neuronal bundles showed stable and chronic antidepressive effects with rapid onset and a higher proportion of patients responding already at lower stimulation intensity than observed in previous studies . The combination of effects suggests that the MFB could be an important future clinical target for neuromodulation in MDD.
The MFB is a key structure of the reward system. It connects (amongst others) the ventral tegmental area (VTA) bidirectionally with the nucleus accumbens (NAC) and the medial prefrontal cortex (mPFC). Typically, the MFB is regarded as a structure that is intimately related to drug abuse and overwhelming reward system activation . Early experimental rodent research on electrical self-stimulation of the brain (ESB) apparently showed detrimental effects on the rodents’ health inducing apparent “self-starvation” . These studies had a very complicated and specific design in terms of food deprivation periods and were later repeated with similar results using other novelty stress signals than ESB of the MFB. Surprisingly, the results were similar [15, 16]. Although the results of the first experiments were later brought into a different perspective, the key message that endured over the years was the incompatibility of MFB stimulation with the welfare of the animal. Thus it is important to study the feasibility and the health implications of continuous MFB DBS in the rodent under more physiological conditions and to know whether further research of DBS of the human MFB is justified. The objective of the current study therefore was to establish chronic and continuous bilateral high frequency stimulation (HFS) of the MFB in rodents, with particular attention given to welfare issues, behavioral effects, postmortem validation of electrode placement, and identification of stimulated pathways. This is an essential first step in the eventual investigation of mechanisms of action and the neurobiological substrates of MFB neuromodulation. All animals received bilateral bipolar electrodes into the MFB at the level of the midbrain ascending dopaminergic projections and, with the exception of the implanted controls, received continuous and chronic stimulation lasting between 3 and 6 weeks. The short- and long-term consequences of the stimulation were analyzed via a combination of behavioral tasks and observations, food and liquid consumption and parameters of indirect metabolic activity, and histological assessment. The results suggest that bilateral MFB stimulation has a robust, reproducible, reversible but moderate impact on the animals’ welfare as shown by the cycle of weight decrease, stabilization, return to pre-DBS weight, and the weight gain following the end of stimulation. MFB stimulation also resulted in neuronal activation in infralimbic and prelimbic cortices, in NAC, and the dorsolateral thalamus, as shown by c-fos expression. Furthermore, the data imply that the dynamics of the transient DBS effect could be dependent on age at the DBS onset. A transient increase in the explorative, searching, and SEEKING type of behavior was measured in the MFB stimulated animals consistent with the proposed role of this structure both in healthy individuals and in clinical depression [11, 17, 18]. Overall, the study demonstrated that the continuous and chronic bilateral stimulation of the MFB in rodents is not detrimental to the animal’s health and can serve as a powerful platform to investigate the effects and mechanisms of neuromodulation in experimental models of depression.
2. Material and Methods
2.1. Animals Housing and Feeding
Young adult female Sprague-Dawley (SD) rats (, Charles River, Germany), weighing 250 g, were housed in individual round cages (height: 40 cm; diameter: 40 cm), with the light/dark cycle maintained at 12 hours on and 12 hours off. Experimental groups and design are summarized in Figure 1. The study described in this paper had the approval of the Ethical Board of the University of Freiburg (Regierungspraesidium; TVA G10-124) and was carried out in accordance with the EU Directive 2010/63/EU concerning the protection of animals used for scientific purposes.
2.2. Surgical Procedures
Rats underwent general anesthesia induced and maintained by inhalation of isoflurane 2%. Skin disinfection was performed and followed by bilaterally stereotactic surgical implantation of custom-made bipolar electrodes into the MFB. Anterior-posterior (AP) and mediolateral (ML) coordinates are taken from bregma, dorsoventral (DV) coordinate from dura. AP = −4.4, ML = ±1.2, and DV = −7.8 . The bipolar probes (125 µm diameter each, 90% platinum/10% iridium, 15 mm long Teflon-coated shaft, World Precision Instruments, Sarasota, USA) were connected to a current isolator and fixed to the skull surface with microscrews and bone cement. Buprenorphine (75 μg/Kg, i.p.) was given to all animals for postoperative analgesia.
2.3. Deep Brain Stimulation
Minimum of 12 days of recovery followed surgery before animals were connected to the pulse generator (STG 2008, Multichannel Systems, Germany) for stimulation. Stimulus pulses consisted of square-wave biphasic, constant current pulse pairs, and stimulation started using clinical relevant parameters (frequency 130 Hz, pulse width 100 μs). Current was individually titrated for each cerebral hemisphere, beginning with 50 μA and increased in units of 50 to a maximum of 350 μA. The final current (mean 288 ± 8 µA) was set 50 µA less than the level that provoked side effects (e.g., rotation, hyperactivity). Safety measures were implemented during the experiment by regularly monitoring voltage and impedance (Hameg Instruments GmbH, Germany) in order to ensure the proper working of the system and to prevent excessive charge that could damage the brain-electrode interface [19, 20]. Based on weight and baseline behavioral data, the 16 animals were split into batches (“DBS A,” “DBS B,” “DBS C,” and control; in all cases). At any one time chronic continuous MFB-HFS was applied to animals for 3 to 6 weeks. The control group had implanted electrodes but did not receive HFS.
2.4. Monitoring Health Status
In earlier investigations, the animals’ welfare following MFB stimulation raised serious issues [14–16]. In the current study, rats were weighed twice a week and food and water were available ad libitum. Food consumed and feces produced were also assessed and used as indicators of metabolic activity .
2.5. Behavioral Assessment
2.5.1. Home Cage Locomotor Activity
Exploratory behavior was evaluated in the home cage at different time points. Animals were filmed for 6 hours (1200–1800)/day for 5 days, with the first day of filming happening prior to turning on the stimulator, and the following days with the stimulator being on; similarly, filming started on the last day the stimulator was on and continued for 4-5 days afterwards. The bottom of the cage was virtually split on the screen into four equal quadrants, and complete line crosses from one quadrant to another area were counted. A blinded assessor scored the recordings.
2.5.2. Forced Swim Test (FST)
FTS is used preclinically to evaluate and screen antidepressant effect of drugs or other treatments in rodents [22, 23]. The protocol consists in placing the animal into a cylindrical receptacle (40 cm height, 20 cm diameter) filled with water (25°C) and measuring the time of activity and immobility. The water level was adjusted so that the rat could not touch the bottom of the container with its tail and could not escape from the cylinder either. Behavior activity was recorded for 5 minutes by a digital video camera connected to the workstation (Viewer2, Biobserve, Germany). The amount of time spent in a posture of immobility was calculated. FST was performed before and after MFB-DBS.
2.5.3. Elevated Plus Maze
Anxiety behavior was assessed by the elevated plus maze test, performed both prior to and after MFB stimulation, according to previous protocol . The animals were placed in the center of the maze, consisting of two open arms and two enclosed arms. The amount of time spent in the open arms (in percent) and the number of entries into the open arms over 5 minutes were assessed (Viewer2, Biobserve, Germany).
2.5.4. Quantifying Sucrose and Water Consumption
Water and 10% sucrose drinking behavior in the home cages was assessed separately at regular intervals over 24-hour observation period including both before and after stimulation.
2.6. Immunohistochemistry and Histological Analysis
Twelve weeks after surgery, animals were terminally anesthetized by an overdose of 10% ketamine (Bela-Pharm GmbH & Co. KG, Germany) and 2% xylazine (Rompun, Bayer-Leverkusen, Germany) and intracardially perfused with a solution containing 4% paraformaldehyde and 0.025% glutaraldehyde in 0.1 M phosphate buffer at pH 7.4. The brains were removed from the skull, kept in 30% sucrose at 4°C until they sunk, and cut into 40 μm coronal sections. The free-floating sections were incubated with 1.5% H2O2, 1% sodium borohydride, and 1% milk powder, each in 0.02 M sodium phosphate buffer at pH 7.4 for 30 min, and exposed to a primary antibody raised in goat against c-fos (SC-52-G, 1 : 2000, lot. number K1808/F1109/A2810, Santa Cruz Biotechnology Inc., Santa Cruz, USA), or mouse anti-ED1 (1 : 1000 #MAB1435, Merck Millipore, KGaA, Darmstadt, Germany). After incubation for 48 h at 4°C, visualization of antibody-binding sites was based on DAB staining using biotinylated anti-goat (BA-5000; 1 : 200; Vector Laboratories, Inc., Burlingame, USA) or biotinylated anti-mouse (BA-2001; 1 : 200; Vector Laboratories, Inc., Burlingame, USA) as secondary antibody and avidin-biotin-technique (ABC Elite; Vector Laboratories, Burlingame, CA) for signal intensification. Finally 3,3′-diaminobenzidine (DAB; Merk, Darmstadt, Germany) and 0.01% H2O2 were used to develop the color reaction. After ED-1-DAB staining, sections were double-stained for Hematoxylin & Eosin (H&E), using a standard protocol. The sections were mounted on super frost plus slides (Langenbrinck, Emmendingen, Germany), dehydrated in ascending alcohol solutions, and cleared in xylene before they were cover slipped with Histofluid (Marienfeld Laborglas, Lauda-Königshofen, Germany) .
Assessment of the final electrode position was carried out by overlapping the H&E histological sections and the respective slice found on a standard stereotaxic rat brain atlas. The final coordinates were then plotted in a schematic figure for optimal visualization of the targeted area. The areas and networks affected by the MFB-HFS were assessed semiquantitatively by microscopically examining (Cell P, Olympus Soft Imaging Solutions, GmbH, Münster, Germany) the pattern of c-fos expression across different regions (Nucleus Accumbens, Prelimbic Cortex, mediodorsal thalamic nuclei and lateral habenula, somatosensory cortex, and dorsolateral striatum). Fos immunolabeling of cellular nucleus in target brain regions was interpreted as an indicator of neuronal activation induced by stimulation of the MFB [26–28].
Two- or three-way ANOVAs with repeated measures was used (Statistica, Germany). In all cases, the main effects were tested for groups (DBS A, DBS B, DBS C, and control) and time (days or periods of DBS or before/after DBS); when analyzing the EPM data, the main effect of arm (open, closed) was also used. When appropriate, post hoc analyses were performed using Student-Newman-Keuls test. Level of significance was set at . Results are expressed as means ± standard error of the mean (SEM).
3.1. Analysis of Health Status
During the study animals were weighed regularly; water and 10% sucrose consumption, food intake, and digestion (via the collection of feces) were monitored. Overall, the treatment did not have a significant bearing on the animals’ weight dynamics (Figure 2; group, ; n.s.). However, MFB-HFS had a robust, but mild and temporary reduction in weight immediately following the onset of the stimulation in all animals (Group × Time, ; ). This phenomenon was manifested as a provisional dip in the growth curve of the animals; following a variable period, despite the continuous stimulation the animals continued to gain weight normally. The relative weight loss was identical (4–6% of prestimulation weight), but the dynamics of it differed across the batches in terms of (i) the number of stimulation days until lowest weight measured and (ii) the number of stimulation days until regaining pre-DBS weight. The data suggests that the effects of the stimulation on the observed parameters are age/weight dependent. DBS A subjects were the youngest (13 weeks) and the lightest (279 ± 9 g) when stimulation started, with the slowest rate of weight loss (maximum after 22 days of MFB-HFS) and the longest recovery time of prestimulation weight (25 days). Following the onset of stimulation, DBS-B (19 weeks/302 ± 11 g) lost weight over 12 days, but recovered prestimulation weight after 19 days. Finally, DBS C rats were the oldest and heaviest (23 weeks/307 ± 5 g) with the quickest rate of reaching the lowest weight (after 7 days) and the fastest recovery of prestimulation weight (16 days). In all three cases, the day when the stimulated animals reached their lowest weight (DBS A, D22; DBS-B, D12; DBS-C, D7), the weight was significantly lower compared to the groups who had not been stimulated yet (Group × Time, , ). The electrode implanted/unstimulated control animals showed continuous weight gain throughout the study. The heterogeneity in the rate and duration of the weight loss might be related to the age and maturation of the CNS of the rats at the time of stimulation, but this needs further experimental evidence.
There was no overall difference across the groups in their average daily dry food consumption (Figure 3(a), Group , n.s.), but when analyzed over time, animals receiving MFB-HFS reduced their intake by about 25% for up to 20 days (Group × Time, , ), which also explains the temporary stimulation induced weight loss. Similarly, overall across the study there were no group differences in feces production (Figure 3(b), group, , n.s.). However, up to 6 days of stimulation, DBS B showed a tendency and DBS C a significant reduction of about 25% in feces production (Group × Time, , ). Importantly when considering welfare issues MFB-HFS did not have an impact on either water consumption (Figure 4(a), Group × Time , n.s.) or 10% sucrose consumption throughout the period of the study nor during the stimulation phases (Figure 4(b), Group × Time , n.s.).
(a) Food intake
(b) Feces weight
(a) Water consumption
(b) 10% sucrose consumption
3.2. Behavioral Assessment
Home cage locomotor activity (HCA) was assessed (i) on the day prior to MFB-HFS and the first 4 days of stimulation and (ii) on the final day of MFB-HFS and the subsequent 4 days with the stimulator off. HCA showed an overall mean increase across animals of 406 ± 220% and 169 ± 39% during the first and second day of stimulation, respectively, compared to the normalized activity levels prior to stimulation. On the final day of activity monitoring, average levels were still above the baseline level (130 ± 33%); however there was variation across batches (Figure 5(a), Group × Day, , ). When the HFS was turned off, on average, the opposite trend was observed: compared to the final day of stimulation, the activity levels decreased to between 89 ± 16% and 84 ± 15% during the following 4 days (Figure 5(b)). However, the overall stimulation duration could have an impact on the HCA measurement after stimulation as DBS B with the shortest stimulation (21 days) manifested the most reduction in activity compared to DBS C (27 days) and DBS A (38 days).
(a) OFF ON
(b) ON OFF
Tests confirmed that the chronic MFB-HFS did not induce any behavioral abnormalities in the animals. Changes in the anxiolytic behavior were measured using the elevated plus maze before and after stimulation in the control and experimental animals. The data shows that all tested animals spent similar percentage of the time in the “closed arm” and that this proportion increased in a similar fashion across the groups between the two testing sessions (Figure 6(a), Group × Session , n.s.). Similarly, performance on the Forced Swim Test, measuring behavioral despair, was not affected by chronic and continuous MFB-HFS (Figure 6(b), Group × Session, , n.s.).
(a) Elevated plus maze
(b) Force Swim Test
The H&E staining confirmed the consistency and accuracy of the bilateral electrode placements (Figures 7(a) and 7(b)). On the right, the mean electrode position was at AP: −4.9 ± 0.10 mm, ML: 0.9 ± 0.05 mm, and DV: −8.2 ± 0.1 mm and on the left side AP: −4.9 ± 0.1 mm, ML: 0.9 ± 0.05 mm, and DV: −8.0 ± 0.10 mm. Two out of 40 electrodes were misplaced or could not be identified in the histological sections (5%). The placement had a mean variation of 0.4 mm in the AP axis compared to the theoretical target; however, this still corresponds to the ascending dopaminergic mesolimbic projections.
Selective stimulation of the ascending ventral mesencephalic DA fibers, that is, originating from the VTA (A10), led to upregulation and increase of c-fos expression in the shell of NAC, prelimbic cortex, mediodorsal thalamic nucleus, and lateral habenula. The semiquantitative assessment of c-fos expression in these terminal structures of the dopaminergic MFB projections revealed a long-lasting upregulation following chronic continuous bilateral MFB-HFS (Table 1). The stimulation induced long-term plastic changes in neural activity as the upregulation was present even in the group DBS A for whom the stimulation seized for up to two months prior to perfusion. Conversely, the dorsolateral striatum that receives dopaminergic neurons mainly from the substantia nigra (A9)  did not present positive staining for this marker suggesting that predominantly the mesolimbic/cortical pathway was stimulated. A subset of animals also received an acute, 2-hour continuous stimulation just prior to perfusion, which resulted in strong upregulation of c-fos, particularly in the prelimbic frontal cortex and shell of the NAC (Figures 8(a)–8(f)).
|– no expression; + mild; ++ moderate; +++ high expression; asterisks indicate a subgroup of animals stimulated for 2 hours preceding perfusion.|
Acute electrical stimulation targeting the medial forebrain bundle (MFB) and associated pathways have been investigated in preclinical models of psychiatric disorders [30–33]; however, the consequences of chronic and continuous MFB stimulation have not been previously studied. The current experiment focused on welfare issues concerning bilateral chronic continuous high frequency stimulation (HFS) of the MFB in rats. The results confirm that clinically relevant stimulation parameters and conditions are feasible and safe and do not impose any apparent long-term welfare issues or behavioral changes in normal, nonpathological experimental animals. MFB-HFS induced acute neural activation resulting in the upregulation of c-fos expression in ascending target areas such as in the shell of NAC, infralimbic and prelimbic cortex, mediodorsal thalamic nucleus, and lateral habenula. Neural activation was observed even at two months following the end of stimulation suggesting that the MFB-HFS can induce long-lasting neural adaptation in pathway activity.
4.1. The MFB in Affective Neuroscience
The rodent MFB stretches from the ventral tegmental area (VTA) in the midbrain to several forebrain structures and includes both myelinated and short typically unmyelinated ascending and descending projections. Studies describe up to 50 fiber subcomponents and 13 neurotransmitters associated with the MFB [34–37], and novel regulatory elements of the MFB are still being discovered . The MFB hosts the mesolimbic and the mesocortical fibers connecting the midbrain dopaminergic (DA) neurons of the VTA to the NAC and the prefrontal cortex, subserving reward, motivational, and learning pathways, and associated with the neural circuitry of psychiatric disorders such as addiction and depression [29, 39]. Crucially, within the framework of affective neuroscience, the ascending DA projections are considered as the neural substrate for the SEEKING system, one of several hard-wired primary affective systems, which ensures positive emotional and euphoric behaviors supporting exploration and modifies appetitive learning [17, 18, 40–42]. Key symptoms in clinical depression and in experimental models, such as anhedonia and helplessness, are thought to be the result of the hypoactivity of the SEEKING system, and the modulation of this system is considered as a potential therapeutic strategy [18, 42].
4.2. Feasibility and Safety of Bilateral Continuous and Chronic MFB-HFS
Early experiments by Olds and Milner and later by many others using intracranial self-stimulation (ICSS) of the MFB set the ground for research into the neurobiology of addiction, reward, and motivation [43–45]. However, historical data suggested that long-term and continuous stimulation of the MFB is not viable as it is detrimental to the animals’ health. A series of studies showed rats implanted with MFB electrodes, when given the choice between self-stimulation and food, would choose self-stimulation over food even when this leads to starvation. The prevailing idea over the last four decades was that the rewarding effect of MFB stimulation trumps the need to eat [14–16].
The current results unambiguously refute this preconceived idea. Animals with electrodes implanted bilaterally into MFB, external to the VTA, but affecting the transmission of ascending midbrain A10 dopaminergic neurons, received continuous clinically relevant HFS up to 6 weeks. Although the stimulation had a reproducible impact on the animals’ weight, food intake, and metabolism, changes in these parameters were temporary and affected mildly the animals’ welfare. The weight decrease, observed immediately with onset of MFB-HFS, stabilized within 1–3 weeks and was followed by sustained weight gain despite the ongoing, chronic electrical stimulation. The start of MFB stimulation also coincided with an temporary (observed up to 72 hours) increase in the explorative, searching, and SEEKING type of behavior, which is consistent with the function of the MFB [17, 40] (see Video 1 in Supplementary Material available online at http://dx.doi.org/10.1155/2015/256196). However, even during the period of weight loss, the chronic and continuous MFB-HFS did not affect the animals’ water or sucrose consumption suggesting that the animals continued to have and could meet their physiological needs. Furthermore, the chronic MFB-DBS did not produce any apparent functional impairment as measured by tests of anxiety or behavioral despair in the normal, nonpathological experimental animals used.
There are several reasons why the current results contrast with the historical data. Since Olds and Milner, electrical stimulation in preclinical studies has been synonymous with ICSS, and it is only during the last 10–15 years that DBS has been adapted to preclinical studies. Routtenberg’s works are convincing within the context they were performed in, but there are crucial differences between “rat-led” ICSS and “investigator-led” DBS experimental designs. Firstly, in ICSS there is the crucial conditioned association between an action and the subsequent reward sensation, which urges the animals to persevere with the lever pressing. In the current study, the MFB stimulation was chronic and this was not conducive for an association to be constructed between the rat’s action and the sensation produced by the HFS. Secondly, in the historical studies animals were given the choice between food and the more salient ICSS of the reward pathway. In the current study, animals had no options but had ad libitum food access. ICSS has proved to be an excellent tool to study addiction and reward pathways [31, 32]. However, between the two types of preclinical electrical stimulation, DBS is more refined and adapts to altering pathological behaviors or modulating deregulated neural pathways.
4.3. Multiple Target Activation following MFB-HFS
Over the years the stimulations of numerous regions associated with the neurocircuitry of depression have been targeted in depressed patients. Stimulations of the subgenual cingulate cortex (Cg25), the ventral capsule/ventral striatum, or the NAC have shown variable response and remission rates [1, 6, 46, 47]. Following the superolateral MFB stimulation, robust antidepressant efficacy in patients was observed within days as opposed to a longer timescale seen in other studies [9, 48]. The reason for the near-immediate effect is not yet known; however, it could be due to the position and the capacity of the MFB to modulate/synchronize the function of all the other key structures implicated in the network. For example, MFB stimulation has been shown to increase the activity in mesolimbic and mesocortical dopamine pathways by enhancing descending glutamatergic excitatory afferents to the VTA and thereby increasing VTA cell firing [49–51]. Stimulation could also influence VTA activity, leading to symptom relief, by increasing lateral hypothalamic (LH) orexin release in the VTA [52–54] or via LH’s GABAergic afferents in the VTA . Additional preclinical studies in validated animal models of depression, for example, incorporating micro-PET or in vivo voltammetry methods, are needed to shed light on the neural basis of MFB-HFS’s antidepressive effect .
Other investigators have shown that DBS induced neural network activation can be followed by looking at the expression of the protooncogene, c-fos, and subsequent synthesis of Fos proteins, via immunohistochemistry [26, 27]. The current study confirmed that MFB stimulation can modulate neuronal activity in multiple regions: following HFS, robust upregulation of c-fos was observed in the shell of the NAC, infralimbic and prelimbic cortex, somatosensory cortex, mediodorsal thalamic nucleus, and lateral habenula. Similar patterns of c-fos upregulation were described by others following short-term ICSS of the MFB [27, 28]. However, in addition to demonstrating short-term modulation, lasting 1-2 hours, the current study has also shown long-term adaptation in neural activity in multiple targets as increased c-fos activity was sustained for up to two months following the end of stimulation.
Recent clinical work targeting the MFB by DBS in treatment resistant depression confirmed the MFB as a promising target that should be investigated more preclinically. The current study demonstrated two critical points. Firstly, continuous and chronic bilateral stimulation of the MFB in rodents is safe and without any consequences on welfare: the approach can be integrated into future investigations of neuromodulation in validated experimental models of depression. Secondly, MFB stimulation results in neuronal activation of multiple regions implicated in the neurocircuitry of depression, such as prefrontal areas, including infralimbic and prelimbic cortices, the NAC, and the dorsolateral thalamus, as shown by upregulation of c-fos expression. This confirms the strategic position of the MFB as its stimulation recruits multiple afferent and efferent connections, inducing short- and long-term plastic adaptations in local and distal neuronal activity. The platform represents a powerful preclinical tool to investigate the role and the neurobiological substrates of the MFB and its associated pathways and targets in the treatment of depression.
Volker A. Coenen has received limited honoraries and travel support as a consultant for Medtronic Europe and limited support for investigator initiated trials from Medtronic (Europe, USA), but these institutions had no role in the design, data collection, interpretation, or preparation of the paper.
Conflict of Interests
Luciano L. Furlanetti, Máté D. Döbrössy, and Iñigo A. Aranda have no conflict of interests to disclose.
Luciano L. Furlanetti and Máté D. Döbrössy contributed equally to the paper.
The authors acknowledge the technical support of Johanna Wessolleck and Marlene Löffler. This research was partly supported by the Stereotactic and Functional Neurosurgery Department, University Hospital, Freiburg, Germany, and the Brain-Links-BrainTools Cluster of Excellence funded by the German Research Foundation (DFG, Grant no. EXC 1086). Luciano L. Furlanetti has a grant from the Deutscher Akademischer Austauschdienst (DAAD) and Brazilian National Council for Scientific and Technological Development (CNPq).
The video clip presents SEEKING behavior induced by chronic continuous bilateral bipolar stimulation of the medial forebrain bundle in a rat, during the titration phase of our stimulation protocol. The video starts showing the animal's expected behavior in OFF condition. During the first few seconds of stimulation ON, visual fixation and freezing behavior can be observed, followed immediately by intensive sniffing and subsequent persistent explorative behavior of the home-cage and surrounding environment. The anti-TH micrographs enclosed in the video indicate the positioning of the stimulating electrodes in the MFB. MFB: Medial Forebrain Bundle; NAC: Nucleus Accumbens; CPu: Striatum; SNc: Substantia Nigra pars compacta; VTA: Ventral Tegmental Area; RRF: Retrorubral field. Yellow spots on the micrographs schematically represent the electric field within the stimulated area.
- R. J. Anderson, M. A. Frye, O. A. Abulseoud et al., “Deep brain stimulation for treatment-resistant depression: efficacy, safety and mechanisms of action,” Neuroscience and Biobehavioral Reviews, vol. 36, no. 8, pp. 1920–1933, 2012.
- T. E. Schlaepfer and K. Lieb, “Deep brain stimulation for treatment of refractory depression,” The Lancet, vol. 366, no. 9495, pp. 1420–1422, 2005.
- T. E. Schlaepfer, B. Bewernick, S. Kayser, and D. Lenz, “Modulating affect, cognition, and behavior—prospects of deep brain stimulation for treatment-resistant psychiatric disorders,” Frontiers in Integrative Neuroscience, vol. 5, article 29, 2011.
- A. S. Taghva, D. A. Malone, and A. R. Rezai, “Deep brain stimulation for treatment-resistant depression,” World Neurosurgery, vol. 80, no. 3-4, pp. S27.e17–S27.e24, 2013.
- A. Sartorius, K. L. Kiening, P. Kirsch et al., “Remission of major depression under deep brain stimulation of the lateral habenula in a therapy-refractory patient,” Biological Psychiatry, vol. 67, no. 2, pp. e9–e11, 2010.
- D. A. Malone Jr., D. D. Dougherty, A. R. Rezai et al., “Deep brain stimulation of the ventral capsule/ventral striatum for treatment-resistant depression,” Biological Psychiatry, vol. 65, no. 4, pp. 267–275, 2009.
- H. S. Mayberg, A. M. Lozano, V. Voon et al., “Deep brain stimulation for treatment-resistant depression,” Neuron, vol. 45, no. 5, pp. 651–660, 2005.
- H. E. McNeely, H. S. Mayberg, A. M. Lozano, and S. H. Kennedy, “Neuropsychological impact of Cg25 deep brain stimulation for treatment-resistant depression: preliminary results over 12 months,” The Journal of Nervous & Mental Disease, vol. 196, no. 5, pp. 405–410, 2008.
- T. E. Schlaepfer, B. H. Bewernick, S. Kayser, B. Mädler, and V. A. Coenen, “Rapid effects of deep brain stimulation for treatment-resistant major depression,” Biological Psychiatry, vol. 73, no. 12, pp. 1204–1212, 2013.
- H. S. Mayberg, “Limbic-cortical dysregulation: a proposed model of depression,” Journal of Neuropsychiatry and Clinical Neurosciences, vol. 9, no. 3, pp. 471–481, 1997.
- V. A. Coenen, J. Panksepp, T. A. Hurwitz, H. Urbach, and B. Mädler, “Human medial forebrain bundle (MFB) and anterior thalamic radiation (ATR): imaging of two major subcortical pathways and the dynamic balance of opposite affects in understanding depression,” Journal of Neuropsychiatry and Clinical Neurosciences, vol. 24, no. 2, pp. 223–236, 2012.
- G. Paxinos and C. Watson, The Rat Brain in Stereotaxic Coordinates, Academic Press, 6th edition, 2007.
- R. A. Wise, P. Bauco, W. A. Carlezon Jr., and W. Trojniar, “Self-stimulation and drug reward mechanisms,” Annals of the New York Academy of Sciences, vol. 654, pp. 192–198, 1992.
- A. Routtenberg and J. Lindy, “Effects of the availability of rewarding septal and hypothalamic stimulation on bar pressing for food under conditions of deprivation,” Journal of Comparative and Physiological Psychology, vol. 60, no. 2, pp. 158–161, 1965.
- A. Routtenberg and A. W. Kuznesof, “Self-starvation of rats living in activity wheels on a restricted feeding schedule,” Journal of Comparative and Physiological Psychology, vol. 64, no. 3, pp. 414–421, 1967.
- A. Routtenberg, “‘Self-starvation’ of rats living in activity wheels: adaptation effects,” Journal of Comparative and Physiological Psychology, vol. 66, no. 1, pp. 234–238, 1968.
- A. Alcaro and J. Panksepp, “The SEEKING mind: primal neuro-affective substrates for appetitive incentive states and their pathological dynamics in addictions and depression,” Neuroscience & Biobehavioral Reviews, vol. 35, no. 9, pp. 1805–1820, 2011.
- V. A. Coenen, T. E. Schlaepfer, B. Maedler, and J. Panksepp, “Cross-species affective functions of the medial forebrain bundle—implications for the treatment of affective pain and depression in humans,” Neuroscience & Biobehavioral Reviews, vol. 35, no. 9, pp. 1971–1981, 2011.
- J. B. Ranck Jr., “Which elements are excited in electrical stimulation of mammalian central nervous system: a review,” Brain Research, vol. 98, no. 3, pp. 417–440, 1975.
- D. Harnack, C. Winter, W. Meissner, T. Reum, A. Kupsch, and R. Morgenstern, “The effects of electrode material, charge density and stimulation duration on the safety of high-frequency stimulation of the subthalamic nucleus in rats,” Journal of Neuroscience Methods, vol. 138, no. 1-2, pp. 207–216, 2004.
- P. Mueller and J. Diamond, “Metabolic rate and environmental productivity: well-provisioned animals evolved to run and idle fast,” Proceedings of the National Academy of Sciences of the United States of America, vol. 98, no. 22, pp. 12550–12554, 2001.
- R. D. Porsolt, G. Brossard, C. Hautbois, and S. Roux, “Rodent models of depression: forced swimming and tail suspension behavioral despair tests in rats and mice,” in Current Protocols in Neuroscience, J. N. Crawley, Ed., chapter 8, unit 8.10A, 2001.
- D. A. Slattery and J. F. Cryan, “Using the rat forced swim test to assess antidepressant-like activity in rodents,” Nature Protocols, vol. 7, no. 6, pp. 1009–1014, 2012.
- S. L. Handley and S. Mithani, “Effects of alpha-adrenoceptor agonists and antagonists in a maze-exploration model of ‘fear’-motivated behaviour,” Naunyn-Schmiedeberg's Archives of Pharmacology, vol. 327, no. 1, pp. 1–5, 1984.
- K. K. Cordeiro, J. G. Cordeiro, L. L. Furlanetti et al., “Subthalamic nucleus lesion improves cell survival and functional recovery following dopaminergic cell transplantation in parkinsonian rats,” European Journal of Neuroscience, vol. 39, no. 9, pp. 1474–1484, 2014.
- J. Klein, M. L. Soto-Montenegro, J. Pascau et al., “A novel approach to investigate neuronal network activity patterns affected by deep brain stimulation in rats,” Journal of Psychiatric Research, vol. 45, no. 7, pp. 927–930, 2011.
- A. Arvanitogiannis, C. Flores, J. G. Fpfaus, and P. Shizgal, “Increased ipsilateral expression of Fos following lateral hypothalamic self-stimulation,” Brain Research, vol. 720, no. 1-2, pp. 148–154, 1996.
- C. Flores, A. Arvanitogiannis, and P. Shizgal, “Fos-like immunoreactivity in forebrain regions following self-stimulation of the lateral hypothalamus and the ventral tegmental area,” Behavioural Brain Research, vol. 87, no. 2, pp. 239–251, 1997.
- S. J. Russo and E. J. Nestler, “The brain reward circuitry in mood disorders,” Nature Reviews Neuroscience, vol. 14, no. 9, pp. 609–625, 2013.
- D. Corbett and R. A. Wise, “Intracranial self-stimulation in relation to the ascending dopaminergic systems of the midbrain: a moveable electrode mapping study,” Brain Research, vol. 185, no. 1, pp. 1–15, 1980.
- W. A. Carlezon Jr. and E. H. Chartoff, “Intracranial self-stimulation (ICSS) in rodents to study the neurobiology of motivation,” Nature Protocols, vol. 2, no. 11, pp. 2987–2995, 2007.
- H. Sagara, T. Sendo, and Y. Gomita, “Evaluation of motivational efects induced by intracranial self-stimulation behavior,” Acta Medica Okayama, vol. 64, no. 5, pp. 267–275, 2010.
- E. Rea, J. Rummel, T. T. Schmidt et al., “Anti-anhedonic effect of deep brain stimulation of the prefrontal cortex and the dopaminergic reward system in a genetic rat model of depression: an intracranial self-stimulation paradigm study,” Brain Stimulation, vol. 7, no. 1, pp. 21–28, 2014.
- L. M. G. Geeraedts, R. Nieuwenhuys, and J. G. Veening, “Medial forebrain bundle of the rat. IV. Cytoarchitecture of the caudal (lateral hypothalamic) part of the medial forebrain bundle bed nucleus,” Journal of Comparative Neurology, vol. 294, no. 4, pp. 537–568, 1990.
- L. M. G. Geeraedts, R. Nieuwenhuys, and J. G. Veening, “Medial forebrain bundle of the rat: III. Cytoarchitecture of the rostral (telencephalic) part of the medial forebrain bundle bed nucleus,” Journal of Comparative Neurology, vol. 294, no. 4, pp. 507–536, 1990.
- R. Nieuwenhuys, L. M. G. Geeraedts, and J. G. Veening, “The medial forebrain bundle of the rat. I. General introduction,” Journal of Comparative Neurology, vol. 206, no. 1, pp. 49–81, 1982.
- J. G. Veening, L. W. Swanson, W. M. Cowan, R. Nieuwenhuys, and L. M. Geeraedts, “The medial forebrain bundle of the rat. II. An autoradiographic study of the topography of the major descending and ascending components,” Journal of Comparative Neurology, vol. 206, no. 1, pp. 82–108, 1982.
- R. Bourdy and M. Barrot, “A new control center for dopaminergic systems: pulling the VTA by the tail,” Trends in Neurosciences, vol. 35, no. 11, pp. 681–690, 2012.
- A. F. T. Arnsten and K. Rubia, “Neurobiological circuits regulating attention, cognitive control, motivation, and emotion: disruptions in neurodevelopmental psychiatric disorders,” Journal of the American Academy of Child and Adolescent Psychiatry, vol. 51, no. 4, pp. 356–367, 2012.
- J. Panksepp, Affective Neuroscience: The Foundations of Human and Animal Emotions, Oxford University Press, New York, NY, USA, 1998.
- J. Panksepp, “The basic emotional circuits of mammalian brains: do animals have affective lives?” Neuroscience and Biobehavioral Reviews, vol. 35, no. 9, pp. 1791–1804, 2011.
- M. D. Döbrössy, L. L. Furlanetti, and V. A. Coenen, “Electrical stimulation of the medial forebrain bundle in pre-clinical studies of psychiatric disorders,” Neuroscience & Biobehavioral Reviews, vol. 49, pp. 32–42, 2015.
- G. F. Koob and N. D. Volkow, “Neurocircuitry of addiction,” Neuropsychopharmacology, vol. 35, no. 1, pp. 217–238, 2010.
- J. Olds, “Self-stimulation experiments,” Science, vol. 140, no. 3563, pp. 219–220, 1963.
- J. Olds and P. Milner, “Positive reinforcement produced by electrical stimulation of the septal area and other regions of rat brain,” Journal of Comparative and Physiological Psychology, vol. 47, no. 6, pp. 419–427, 1954.
- B. H. Bewernick, S. Kayser, V. Sturm, and T. E. Schlaepfer, “Long-term effects of nucleus accumbens deep brain stimulation in treatment-resistant depression: evidence for sustained efficacy,” Neuropsychopharmacology, vol. 37, no. 9, pp. 1975–1985, 2012.
- A. M. Lozano, P. Giacobbe, C. Hamani et al., “A multicenter pilot study of subcallosal cingulate area deep brain stimulation for treatment-resistant depression: clinical article,” Journal of Neurosurgery, vol. 116, no. 2, pp. 315–322, 2012.
- V. A. Coenen, B. Mädler, and T. E. Schlaepfer, “Reply to: Medial forebrain bundle stimulation—speed access to an old or entry into a new depression neurocircuit?” Biological Psychiatry, vol. 74, no. 12, pp. e45–e46, 2013.
- S. Ikemoto and R. A. Wise, “Mapping of chemical trigger zones for reward,” Neuropharmacology, vol. 47, supplement 1, pp. 190–201, 2004.
- S. Ikemoto, “Brain reward circuitry beyond the mesolimbic dopamine system: a neurobiological theory,” Neuroscience and Biobehavioral Reviews, vol. 35, no. 2, pp. 129–150, 2010.
- A. Friedman, E. Lax, L. Abraham, H. Tischler, and G. Yadid, “Abnormality of VTA local field potential in an animal model of depression was restored by patterned DBS treatment,” European Neuropsychopharmacology, vol. 22, no. 1, pp. 64–71, 2012.
- C. Nocjar, J. Zhang, P. Feng, and J. Panksepp, “The social defeat animal model of depression shows diminished levels of orexin in mesocortical regions of the dopamine system, and of dynorphin and orexin in the hypothalamus,” Neuroscience, vol. 218, pp. 138–153, 2012.
- G. Aston-Jones, R. J. Smith, G. C. Sartor et al., “Lateral hypothalamic orexin/hypocretin neurons: a role in reward-seeking and addiction,” Brain Research, vol. 1314, pp. 74–90, 2010.
- T. E. Scammell and C. B. Saper, “Orexin, drugs and motivated behaviors,” Nature Neuroscience, vol. 8, no. 10, pp. 1286–1288, 2005.
- M. B. Lassen, J. E. Brown, S. H. Stobbs et al., “Brain stimulation reward is integrated by a network of electrically coupled GABA neurons,” Brain Research, vol. 1156, no. 1, pp. 46–58, 2007.
Copyright © 2015 Luciano L. Furlanetti et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.