Abstract
Rationale
In addition to the disease-defining motor symptoms, patients with Parkinson’s disease (PD) exhibit gait dysfunction, postural instability, and a propensity for falls. These dopamine (DA) replacement-resistant symptoms in part have been attributed to loss of basal forebrain (BF) cholinergic neurons and, in interaction with striatal dopamine (DA) loss, to the resulting disruption of the attentional control of balance and complex movements. Rats with dual cholinergic-DA losses (“DL rats”) were previously demonstrated to model PD falls and associated impairments of gait and balance.
Objectives
We previously found that the muscarinic M1-positive allosteric modulator (PAM) TAK-071 improved the attentional performance of rats with BF cholinergic losses. Here, we tested the hypotheses that TAK-071 reduces fall rates in DL rats.
Results
Prior to DL surgery, female rats were trained to traverse a rotating straight rod as well as a rod with two zigzag segments. DL rats were refamiliarized with such traversals post-surgery and tested over 7 days on increasingly demanding testing conditions. TAK-071 (0.1, 0.3 mg/kg, p.o.) was administered prior to daily test sessions over this 7-day period. As before, DL rats fell more frequently than sham-operated control rats. Treatment of DL rats with TAK-071 reduced falls from the rotating rod and the rotating zigzag rod, specifically when the angled part of the zigzag segment, upon entering, was at a steep, near vertical angle.
Conclusions
TAK-071 may benefit complex movement control, specifically in situations which disrupt the patterning of forward movement and require the interplay between cognitive and motor functions to modify movement based on information about the state of dynamic surfaces, balance, and gait.
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Introduction
In addition to the nigrostriatal dopamine (DA) deficiency and the associated efficacy of dopaminergic replacement therapy (DRT) to reduce motor symptoms, progressing Parkinson disease (PD) is characterized by neurodegeneration in non-DA systems and associated DRT nonresponsive features such as gait and balance disorder, postural instability, and cognitive impairments. Given the severe medical consequences of a resulting increase in the propensity for falls, investigating the pathophysiology underlying falls and the development of treatments to reduce fall risk are important objectives (Albin et al. 2018a; Weaver et al. 2016; Li et al. 2015; Paul et al. 2014; Cheng et al. 2014; Shine et al. 2013; Kehagia et al. 2013; Heremans et al. 2013; Amboni et al. 2013; Montero-Odasso et al. 2012; Fasano et al. 2012; Cole et al. 2011; Taylor et al. 2009; Stack and Ashburn 2008; Langston 2006; Grimbergen et al. 2004).
Loss of cholinergic projections, which arise from the basal forebrain (BF) and innervate virtually all cortex as well as several thalamic nuclei, has been associated with increased falls in PD (Bohnen et al. 2019; Muller et al. 2013; Bohnen and Albin 2011; Bohnen et al. 2009; Rochester et al. 2012; Albin et al. 2018b). Cortical cholinergic signaling is necessary for the integration of exteroceptive and interoceptive cues into ongoing behavior, thereby permitting these cues to influence and, if previously associated with defined responses, control behavior (Sarter and Lustig 2020; Lu et al. 2020; Howe et al. 2017; Gritton et al. 2016; Berry et al. 2014; Howe et al. 2013; Parikh et al. 2007; Venkatesan et al. 2020; Picciotto et al. 2012). Therefore, PD falls have been extensively demonstrated to be closely associated with a decline in such attentional capacities (Stuart et al. 2017; Yarnall et al. 2011; Lord et al. 2010; Cools et al. 2010; Allcock et al. 2009; Yogev-Seligmann et al. 2008; Shumway-Cook and Woollacott 2000; Chen et al. 1996; Stam et al. 1993; Kim et al. 2017, 2019; Berry et al. 2017).
We previously developed a rodent model of PD falls by demonstrating that rats with dual basal forebrain cholinergic and mediodorsal striatal DA losses (“DL rats”) exhibit a heightened fall rate when required to traverse dynamic surfaces. A new behavioral set of tasks, called the Michigan Complex Movement Control Task (MCMCT), was shown to produce falls in DL rats that reflect the disruption of attentional-motor integration. Falls in DL rats were correlated with impairments in their sustained attention performance. Moreover, such falls were associated with behavioral risk factors comparable to those seen in PD fallers, including slower traversal speed, postural inefficiencies, and impairments in turning behavior. Correlations between cholinergic and dopaminergic losses and fall rates indicated that cholinergic losses unmask striatal deficits in the selection and sequencing of movements, particularly when movement corrections were triggered by paw misplacements or balancing errors (Avila et al. 2020; Koshy Cherian et al. 2019; Kucinski et al. 2017; Kucinski and Sarter 2016; Sarter et al. 2014; Kucinski et al. 2013). Thus, the performance of DL rats on the MCMCT specifically models falls resulting from a disruption of the brain’s cognitive-motor interface.
The present experiment was designed to test the hypothesis that treating DL rats with a muscarinic M1 acetylcholine receptor (mAChR)–positive allosteric modulator (PAM) reduces their fall rate. The focus on M1 receptors as a key node in the attention-mediating functions of the BF cholinergic system in part arises from evidence showing that the cholinergic mediation of attention requires the M1-mediated generation of high-frequency oscillations in the cortex and of neuronal synchrony across multiple frequency bands (Howe et al. 2017; see also Moran et al. 2019; Gould et al. 2015; Herrero et al. 2008; Disney and Aoki 2008; Lu et al. 2020). Such M1-mediated effects are thought to orchestrate multiple neuronal populations for integrating the cognitive, sensory, and motor components of a cue-evoked behavioral response. A PAM-mediated amplification of such M1-dependent neuronal activity patterns would be expected to enhance and, in DL rats, rescue important aspects of the postsynaptic impact of cholinergic signals. As a result, such a treatment would be expected to benefit the ability of DL rats to more effectively employ task cues as well as utilize proprioceptive information to optimize dynamic surface traversal, and to respond to movement errors by rapidly adapting gait and balance to continue forward traversal. We tested this hypothesis using the M1 PAM TAK-071 because of this compound’s relatively high selectivity for neuronal M1 receptors (Kurimoto et al. 2019; Sako et al. 2018) and based on our prior finding that this drug improves the attentional performance of rats with BF cholinergic lesions (Kucinski et al. 2020). In addition to testing fall propensity in rats traversing the rotating rod of the MCMCT, we also assessed their ability to traverse a rotating zigzag rod which even more severely taxes the attentional control of balance and complex movements (Kucinski et al. 2019; Kucinski et al. 2018). The main results indicate a TAK-071-induced reduction in fall rate primarily in the latter condition, and specifically in interaction with “steep” zigzag entry angles that require rapid and continuous postural re-balancing and gait adjustment.
Materials and methods
Subjects
Forty adult female Sprague Dawley rats (Envigo) between 2 and 3 months of age, weighing 273.79 ± 2.78 g (M, SEM) at the beginning of experiments, were used for these experiments. We previously observed that male rats exhibited more falls and traversed rods more slowly than female rats, particularly on the zigzag rod (Fig. 1). In addition to evidence suggesting relatively superior attentional control of complex movement in female rats, we also found that falls in male rats were associated with their relatively higher body weights (Kucinski et al. 2019; Koshy Cherian et al. 2019; Kucinski et al. 2017; Kucinski et al. 2018). Furthermore, we previously documented beneficial attentional effects of TAK-071 in male and female rats with basal forebrain cholinergic lesions, and also in female, but not male, control rats (Kucinski et al. 2020). As the present experiments were designed to determine whether these effects generalize to complex movement control, as assessed specifically by traversal of the zigzag rod, only female rats were used to optimize the documentation of such effects. As was previously discussed, such sex effects in rats may primarily inform about the cognitive-motor constraints of the efficacy of this behavioral test and the pharmacological intervention, rather than pointing to potentially equivalent sex effects in other species.
Rats were handled daily for at least 3 days prior to beginning behavioral training and received 10–20 banana pellets (45 mg per pellet; BioServ) daily for 3 days prior to the start of testing. Animals were individually housed in opaque single standard cages (27.70 cm × 20.30 cm) in a temperature- and humidity-controlled environment (23 °C, 45%) and maintained under a 12:12-h light/dark schedule (lights on at 8:00 AM). Food (Envigo Teklad rodent diet) and water were available ad libitum. Estrous cycle was not determined. All procedures were conducted in adherence with protocols approved by the University Committee on Use and Care of Animals at the University of Michigan and in laboratories accredited by the Association for Assessment and Accreditation of Laboratory Animal Care.
Michigan Complex Movement Control Task
The MCMCT beam traversal apparatus (Kucinski et al. 2013; Kucinski et al. 2019; Kucinski et al. 2018; Sarter et al. 2014; Koshy Cherian et al. 2019; Avila et al. 2020) assesses the ability of rats to perform attention-demanding beam traversals and correct for stepping errors while crossing a “straight” narrow rod or a bended rod surface (“zigzag”; see below). The rods were 3.0 m in length (square; side lengths 1.59 cm), made from aluminum tubing covered with gray gaffer’s tape for traction. There was also a plank surface (13.3 cm width) that could be placed directly on top of the straight rod and fitted firmly in place inside edges of the support towers used to familiarize rats with traversing from goal box to goal box. The straight and zigzag rods could be rotated using a 12 VDC electric motor controlled remotely by a pulse width modulator which was able to adjust the speed of rotation (up to 10 RPM) and switch the direction of rotation. A safety net was suspended 20 cm under the beam to catch the rats during falls. Two identical end stations were situated on top the support towers at opposite ends of the beam. These stations consisted of a 30 × 25-cm platform with a 3-cm diameter copper cup embedded in the floors. During training and testing, rats were given a banana pellet placed inside the cups in the goal boxes following each traversal. Each goal box was surrounded by a retractable wall structure (23 cm height in raised position) to allow for conversion from an open platform to a boxed structure. On the wall facing the beam of each box structure, a 9-cm wide opening allowed the rats access to and from the beam. The walls were raised and lowered mechanically with a 12 VDC electric motor actuated remotely by a toggle switch. Lowering the walls and thereby turning the box into an open-field platform was sufficient for rats to initiate beam traversal to enter the opposite box (with walls up) and consume the banana pellet. Between traversals, the walls of the goal boxed remained in the up-position for 45 s. Videos of traversals were recorded with 4 bullet Marshall 1080-HD-DI model CV500 Series cameras (B-30/25P frame rate/59.94i) mounted on the net frame parallel to one side of the beam. The videos were converted to a single feed using a quad SDI to HDMI multiviewer (Matrox MicroQuad) and viewed directly on a PC using Elgato Game Capture HD software.
Straight rotating rod
Performance measures were falls and traversal time on the straight rotating rod. These measures were analyzed in the same manner as previously described (Kucinski et al. 2017; Kucinski et al. 2013). Rats were allowed to fall into the net and placed back onto the rod or, upon an imminent fall, the experimenter assisted the rat in regaining balance on the rod, and no further falls were counted until the rat regained a balanced posture and resumed forward movement. In addition to complete falls from the straight rod (“major falls”), we also counted as falls when the rat would completely cease forward movement and assume a slouched, nearly immobile position on the rod (“minor falls”). In either case, traversal time was corrected for fall-related disruptions of forward movement. In the overwhelming number of cases, rats were able to regain forward movement within 2 s of being placed back onto the rod. Because multiple falls could occur during a run, falls per run were used as a metric for fall rates. We previously reported high inter-rater reliability for extracting the behavioral measures from videotaped MCMCT runs (Avila et al. 2020).
Zigzag rotating rod
A zigzag rod variation was designed to particularly severely tax complex movement control (Kucinski et al. 2019; Kucinski et al. 2018). This rod (Fig. 1) included two zigzag sections that were each 0.6 m in length and placed 0.6 m from either end of the rod and separated by a 0.6-m-long straight rod in the middle (Fig. 1a). Each zigzag section included three angled sections of varying lengths (two 10.7 cm and one 21.5 cm in length) that bended at 45° angles from the horizontal plane of the rod and that connected to two straight sections (each 15 cm in length) that rested 3 cm above or below the plane, the vertical plane of the rod. The diameter of the rod tube remained 2.54 cm across the entire rod.
The rod could be held stationary either horizontally, so the zigzag sections protruded to the sides thus forcing rats to turn left or right while traversing (Fig. 1b), or so the zigzag sections faced up and down vertically (Fig. 1c, d), or rotated (5 RPM) so that rats were required to perform sideways and vertical movements while navigating over the zigzag sections. In contrast to falls from the straight rod, “minor falls” from the zigzag portions did not occur. Furthermore, performance on the straight parts of the zigzag rod was not analyzed. Thus, fall rates from the two rod types are not directly comparable. In addition to falls, we determined, for each entry, onto the first and second angled part of the zigzag sections: (1) the angle of elevation above or below the horizontal plane at the time when rats entered (an entry was scored when the rat placed its forepaws onto such a section and continued to move onto the angled part), and (2) whether the angled part was rotating upwards (Fig. 1e, f) or downwards (Fig. 1g, h). Angles of elevation at the time of entrance (forepaws placed onto an angled section) were categorized as flat (0–30° away from the horizontal or flat level shown in Fig. 1b); medium steep (31–60°); or steep (61–90°, with 90° depicting the zigzag section in vertical position, facing upward or downward as shown in Fig. 1c, d). Rotation direction (upwards or downwards) was further defined depending on whether the angled part rotated toward a steeper state (Fig. 1e, f) or a flatter state (Fig. 1g, h).
Training and testing regimen
Prior to receiving DL or sham surgeries (below), rats were habituated to the traversal apparatus over a 5-day test sequence, including runs on the plank, nonrotating straight rod, rotating straight rod (5 RPM), and the zigzag surface (nonrotating runs in the vertical and horizontal positions and rotating runs at 5 RPM; Table 1).
Following completion of the pre-surgery MCMCT practice, animals were randomly distributed into two groups, designated to either receive DL surgery (n = 30) or sham surgery (n = 10). Recovery from surgery was between 5 and 10 weeks; this relatively long and variable period of time between surgeries and post-surgery testing was due to the COVID-19-associated cessation of laboratory research. Fourteen rats were tested following a 5-week break and 26 rats were tested following a 10-week period. A post hoc analysis of a potential effect of break duration on fall rates on both the rotating straight rod (combined 3 days) and the zigzag rod (combined two days) did not reveal a main effect of interactions with group (all F < 0.84, P > 0.37). Among the rats which were tested following a 10-week break, the data from 3 sham-operated, and 4 DL rats (one treated with vehicle, two with 0.1 mg/kg, and one with 0.3 mg/kg TAK-071), were removed from the final analysis because these rats failed to traverse the rods. In addition, one sham-operated and one DL/vehicle rat did not traverse the zigzag rod on the final day (day 7) of testing.
Following surgery, the 30 DL rats were randomly divided into 3 groups (10 each) to be treated with either vehicle or 0.1 mg/kg or 0.3 mg/kg TAK-071. Sham-operated rats were treated with vehicle (see below). All rats then underwent a 7-day traversal test sequence (Table 1), including runs on the plank and straight rod surfaces (for re-acclimatization to the testing conditions, day 1), rotating straight rods (days 2, 3, and 4), and the zigzag rods (days 5, 6, and 7).
TAK-071
TAK-071 (Takeda Pharmaceutical Company; Lot # M071-004) was dissolved in 0.5% methyl cellulose in DI water (vehicle). Vehicle and a 0.1-mg/mL stock solution were prepared on the first day of drug administration and kept cool and out of light during the 7-day test sequence. The stability of this preparation was determined by Takeda Pharmaceutical Company (Yuta Arai, Takeda Pharmaceutical Company Limited, unpublished data). Animals were familiarized with gavage administration procedures for five consecutive days prior to the onset of the drug testing period. Rats were administered vehicle (3.0 mL/kg) or drug (0.1 or 0.3 mg/kg) via oral gavage 30 min prior to the onset of the daily test session, for a total of 7 days. The two doses for testing were selected based on pharmacological and pharmacokinetic data (Kurimoto et al. 2019; Sako et al. 2018). Specifically, following oral administration of 0.3 mg/kg, peak brain concentration (Cmax) was 0.11 μM (for plasma and brain concentrations following oral administration of 0.1–10 mg/kg of TAK-071 in rats, see Table S2 in Sako et al. 2018). The brain concentration following oral administration was found to be well above the half maximal concentration for PAM at M1 AChR (2.7 nM), but below concentrations required for PAM at M2-M5 AChRs (> 1000 nM; Sako et al. 2018). TAK-071 is a highly selective PAM, relative to agonist effects at the M1 AChR (EC50: 520 nM; Sako et al. 2018). Following oral administration of 0.1 and 0.3 mg/kg, the half-life of TAK-071 (Tmax: 1.7 h) extended well beyond the period of behavioral testing in the current experiment (30–45 min following administration). Evidence describing the effects of semi-chronic administration of TAK-071 on plasma and brain concentrations appears unavailable. Finally, for the present experiment, the two doses were selected based on our prior study indicating efficacy of these doses, administered over 6 days, in rats with cholinergic lesions and performing a sustained attention task (Kucinski et al. 2020).
Surgeries
Rats were anesthetized with isoflurane gas (induction, 4–5%; maintenance, 2–3%) delivered at 0.6 L/min O2 using a SurgiVet Isotec 4 Anesthesia Vaporizer and mounted to a stereotaxic instrument (David Kopf Instruments, Tujunga, CA). Animal temperatures were maintained at 37 °C using Deltaphase isothermal pads (Braintree Scientific). Ophthalmic ointment was provided for eye lubrication. A subcutaneous injection of 1 mL/100 g 0.9% NaCl solution was administered to prevent hypovolemia and hemodynamic instability. Rats also received carprofen (5 mg/kg; subcutaneous; Henry Schein) for pain relief just prior to individual surgeries. Rats received bilateral bolus infusions (10 μg/μL; 1 μL/hemisphere) of the neurotoxin 6-hydoxydopamine (6-OHDA; Sigma-Aldrich, MO, n = 30) or vehicle (1 mg/mL ascorbic acid in 0.9% NaCl; n = 10) into two sites of the striatum (bregma A/P: + 1.2 or + 0.2 mm, M/L: ± 2.5 or ± 3.0 mm, D/V: − 5.0 mm from dura). Rats were also injected with desipramine hydrochloride (10 mg/kg; i.p.; Sigma-Aldrich) 30 min prior to neurotoxin infusions to protect noradrenergic neurons (Breese and Traylor 1971). Rats received bilateral infusions of the cholino-specific immunotoxin 192 IgG-saporin (200 ng/μL; 0.8 μL/hemisphere; Advanced Targeting Systems, CA, n = 30) or an equal volume of artificial cerebral spinal fluid (n = 10) into the nucleus basalis and substantia innominata of the basal forebrain (BF; bregma A/P: − 0.8 mm, M/L: ± 2.9 mm, D/V: − 7.8 mm). For all infusions, an additional 8 min was allowed for diffusion before the needle was removed. Nonabsorbable nylon sutures were used to close the incisions. Topical antibiotic (Neosporin) was applied to the wounds. Rats received one subsequent dose of carprofen (5 mg/kg) 1 day post-surgery, followed by 5–10 weeks of recovery period before the initiation of behavioral testing.
Histology
Following the completion of the behavioral testing, rats were deeply anesthetized with a lethal dose of sodium pentobarbital (270 mg/kg, i.p.) and transcardially perfused with phosphate-buffered solution (PBS) followed by 4% paraformaldehyde in 0.15 M sodium-phosphate solution, pH 7.4. Brains were extracted and postfixed in 4% paraformaldehyde for 24 h, rinsed with PBS, and then placed in 30% sucrose solution until they sank. Brains were sectioned into 35-μm-thick slices using a freezing microtome (CM 2000R; Leica) and stored in cryoprotectant until further histological processing. Sections from lesioned and sham-lesioned rats were stained, separately, for the visualization of acetylcholinesterase (AChE)-positive fibers in the cortex and the presence of striatal tyrosine hydroxylase (TH). The density of AChE-positive fibers in cortex and TH depletions were quantified as described previously (Avila et al. 2020; Koshy Cherian et al. 2019; Kucinski et al. 2013). Briefly, a 4 × 4 grid of 30-μm (side length) squares was digitally superimposed photographs of AChE-positive fibers in layers 5/6 of primary motor cortex (× 40 magnification). Labeled fibers which crossed one of the lines of the superimposed grid were counted using the ImageJ multipoint tool. The extent of cholinergic loss was quantified for each DL rats by subtracting their individual fiber count from the mean fiber count from sham-lesioned rats (for both hemispheres and then averaged to a single value per rat). The degree of AChE-positive fiber loss was scored from 5 to 1, with 5 indicating the greatest loss of AChE-positive fibers (5: > 90% loss; 4: > 80%; 3: > 70%; 2: > 60%; 1: 30–50% loss). Photographs of TH immuno-stained sections were taken at 1.25× from sections at approximately 500 μm posterior and anterior from the infusion sites at 0.2 AP to 1.2 AP. The extent and location of the bleaching of TH stains was rated. TH-IR losses greater than 2.00 mm (dorsal-ventral plane) × 0.5 mm (medial-lateral plane) × 0.5 mm (anterior-posterior plane) were assigned the highest score (5). Lower scores (≤ 3) were assigned to smaller lesion sizes. We previously determined that TH losses in the mediodorsal part of the striatum, overlapping with the target field of prefrontal cortical projections, are necessary and sufficient to produce falls in DL rats (Kucinski et al. 2015; Kucinski et al. 2013). TH losses centered closest and mostly restricted to the mediodorsal caudate nucleus were assigned the highest score (5), whereas lesions spreading more laterally received scores ≤ 3. The size and placement scores for both hemispheres were averaged to a single DA lesion score for each DL rats. Finally, a composite lesion score was calculated for each DL rats by multiplying the AChE and TH loss depletion score. Thus, a near-complete loss of cortical AChE-positive fibers combined with large mediodorsal striatal TH depletions would receive a rating of 25.
Statistical analyses
For runs on the straight rotating rod, falls and traversal time were compared between the groups (sham-vehicle, DL-vehicle, DL-0.1 mg/kg TAK-071, and DL-0.3 mg/kg TAK-071) using the data from the 4th day of treatment and from runs across which the rotation direction of the rod was alternated (ANOVA). Falls during zigzag beam traversals on days 6 and 7 likewise were analyzed using ANOVA, with alpha set at 0.05/2 for conducting separate analyses. For the post hoc investigation of the impact of entry angle category and rotation direction, falls obtained from the last day of testing were computed over the number of entries per category and over all 6 runs, and analyzed using repeated measures ANOVA of the effects of angle category and group. Post hoc multiple comparisons were conducted using Fisher’s least significance difference (LSD) test. Statistical analyses were performed using the SPSS for Windows (version 17.0: SPSS). Assumptions underlying the statistical model were assessed. In cases of violation of the sphericity assumption, Huyhn-Feldt-corrected F values, along with uncorrected degrees of freedom, are given. Alpha was set at 0.05 except for the analysis of falls from days 6 and 7 (above). Exact P values are reported as recommended previously (Greenwald et al. 1996; Sarter and Fritschy 2008). Effect sizes (Cohen’s d) were calculated for major significant effects and classified in accordance to Cohen (1988).
Results
Straight rotating rod performance in DL rats and effects of TAK-071
Following recovery from surgeries, animals underwent drug testing with TAK-071 or vehicle over a 7 (consecutive)-day traversal sequence (Table 1). TAK-071 or vehicle was administered via gavage 30 min prior to the onset of MCMCT testing on each of the 7 test days. On the first day of testing, rats were refamiliarized with traversing the plank and nonrotating straight rod surfaces. On the second, third, and fourth days, straight rotating rod traversals were assessed (6 runs per day; clockwise (cc) day 1, counterclockwise (cw) day 2, alt direction day 3; 8 RPM for all days; see Fig. 2a for an illustration of the straight rod testing apparatus). Falls and traversal time were extracted from these runs and compared between the four groups (shams treated with vehicle, S-V; DL rats treated with vehicle, DL-V; DL rats treated with 0.1 mg/kg, DL-0.1; or with 0.3 mg/kg TAK-071, DL-0.3), with rotating direction as a within-subjects factor. As cc- and cw-rotating rod traversal was tested early into the treatment regimen, on days 2 and 3, the analysis of straight rotating rod performance was limited to the test of the relatively more demanding condition on the 4th day of treatment, that is, when alternating the rod direction from run to run.
As expected, based on our prior experiments on the performance of DL rats, DL-V rats fell more frequently than S-V rats (main effect of group: F(3,32) = 3.13, P = 0.04; post hoc comparison (LSD): P = 0.03; Cohen’s d: 0.93). Furthermore, DL-0.1 rats fell nearly significantly less than DL-V rats (P = 0.05; Fig. 1b). The size of the near-significant effect of the lower dose of TAK-071 (d: 0.89) was “large” as classified by Cohen (1988).
DL-V rats appeared to require more time traversing the alternatingly rotating rod than S-V and DL-0.1 rats, but the effect of group did not reach significance (F(3,32) = 1.81, P = 0.17; Fig. 1c).
Falls and traversal time were significantly correlated across all groups of rats (R2 − 0.74, P < 0.001) and, with the exception of DL-0.3 rats, also within individual groups (S-V, DL-V, DL-0.1 groups: R2 > 0.65, P < 0.02; DL-0.3: R2 = 0.35, P = 0.09; Fig. 2d). The lack of a significant correlation between traversal time and falls in DL-0.3 rats suggested that, in contrast to the effects of the lower dose of TAK-071, DL-0.3 rats continued to traverse the rod as slowly as DL-V rats while falling at a (nonsignificantly) lower rate than DL-V rats.
Zigzag rod performance in DL rats and effects of TAK-071
On the 5th day of testing (Table 1), rats were refamiliarized with traversing the zigzag rod fixed in the horizontal and vertical position. Next, falls and traversal time were assessed across two consecutive days based on traversals of the alternatingly rotating zigzag rod (5 RPM). Separate analyses for falls from days 6 and 7, with alpha set at 0.05/2, indicated a main effect of group on falls during the second day of rotating zigzag rod testing (F(3,30) = 5.51, P = 0.004) but not on the first test of this condition (F(3,32) = 0.96, P = 0.43). Multiple comparisons indicated that on the second day of traversing the rotating zigzag rod, DL-V rats fell more frequently than all other groups (all P < 0.03; all Cohen’s d > 1.03; Fig. 3a).
To further explore the specific zigzag conditions which were associated with high falls in DL-V rats and the reduction in falls in DL rats treated with TAK-071, we applied a previously established sorting scheme of the status of the zigzag segments (see Fig. 1 for an abbreviated illustration of major zigzag conditions; for more details, see Kucinski et al. 2018). This analysis was based on a total of 744 entries to zigzag segments, obtained from 6 S-V, 8 DL-V, 8 DL-0.1, and 9 DL-0.3 rats (24 entries per rat), and from the second day of alternatingly rotating zigzag runs.
Our initial analysis focused on the possibility of a robust differentiation between the groups for entries into the zigzag portion when the bent parts were sloped 61–90° above or below the horizontal (or “steep”; Fig. 1c, d), because this condition was previously identified as associated with more falls than less steep entry states (Kucinski et al. 2019; Kucinski et al. 2018). First, the total number of entries into the bent sections at one of three angle categories (flat: 0–30°, medium: 31–60°, steep: 61–90°) did not differ between the groups (group × angle category; (χ2(6) = 8.63, P = 0.20). This finding rejects the possibility that certain entry angle categories were avoided by individual groups of rats.
Next, we computed the number of falls per entry category (Fig. 3b). ANOVA of the effects of group and entry angle category (“flat” or 0–30°, see green segments on the left of Fig. 3b; “medium steep” or 31–60°, see yellow segments in the middle of Fig. 3; “steep” or 61–90°, see red segments on the right of Fig. 3b) indicated a significant interaction between the effects of the two factors (F(6,54) = 2.84, P = 0.02; Fig. 3b). In addition, this analysis, of falls per entry category and summed up of all 6 runs (and thus different to the falls per run shown in Fig. 3a), indicated a trend for a main effect of group (F(3,27) = 2.89, P = 0.056), mirroring the data pattern shown in Fig. 3a, and a main effect of entry category (F(2,54) = 28.76, P < 0.001; Fig. 3b). To identify the locus of the interaction between the effects of group and angle category, one-way ANOVAs on the effects of group per angle category indicated a significant effect for the steep (F(3,30) = 4.48, P = 0.01) but not the two less steep angle categories (both P > 0.11). Thus, these analyses indicated that all groups of rats fell relatively more frequently when entering an angled part in the steep orientation, and that this condition revealed the relatively higher fall rate of DL rats as well as a reduction of falls in DL rats treated with TAK-071 (Fig. 3b; Cohen’s d for DL-V versus 0.1 mg/kg: 1.56; 0.3 mg/kg: 0.67). Finally, exploration of the impact of rotation direction (turning the angled part into an even steeper versus a flatter condition) did not provide further insights into the propensity for falls associated with the steep entry angle category (main effect and interaction, both P > 0.27).
Histological findings
The density of AChE-positive fibers in cortex was significantly reduced in all DL groups, with no significant differences between the three groups of DL rats (F(3,31) = 48.95, P < 0.001 (S-V: 65.64 ± 4.35 fibers; DL-V: 21.83 ± 1.20; DL-0.1: 27.64 ± 2.52; DL-0.3: 24.56 ± 2.76; multiple comparisons indicated that fiber counts in all DL rats were significantly lower than in S-V rats, all three P < 0.001). On average, AChE-positive fiber losses received a rating of 2.92 ± 0.22 (see “Materials and methods”), reflecting a loss of about 60% of cholinergic inputs. Likewise, neither the size nor the location of mediodorsal striatal TH losses differed between the three DL groups (size: F(2,24) = 0.08, P = 0.93; score: 2.09 ± 0.15; location: F(2,24) = 0.97, P = 0.40 (score: 3.92 ± 0.17). TH losses in DL rats were previously found to be correlated with fall rates (Avila et al. 2020; Koshy Cherian et al. 2019; Kucinski et al. 2017; Kucinski et al. 2013). The present data did not indicate a significant correlation between TH losses and falls in DL-V rats, likely because of a relatively limited variability of TH losses in these rats. Losses of cortical AChE-positive fibers and striatal TH-immunoractivity were extensively illustrated in prior reports describing experiments involving DL rats (see Avila et al. 2020; Koshy Cherian et al. 2019; Kucinski and Sarter 2015; Kucinski et al. 2015; Kucinski et al. 2013, 2017).
Discussion
DL rats model the combined BF cholinergic and mediodorsal striatal dopaminergic losses which characterize PD fallers. Fall rates were measured in DL rats traversing a rotating straight rod and a rotating zigzag rod. As was expected, DL rats fell more frequently than sham-operated rats in both conditions. Administration of the lower dose of TAK-071, daily over a 7-day period and prior to daily test sessions, nearly significantly reduced falls during rotating rod traversal (P = 0.05; Cohen’s d: 0.89). Both doses of the M1 PAM reduced falls occurring during zigzag rod traversal. In the latter test, the number of falls in DL rats was particularly high, and the M1 PAM was robustly beneficial, when the angled part of the zig zag rod was at a steep, near vertical angle at the time the rats entered a zigzag segment.
The current experiments were conducted using only female rats because prior experiments indicated a relatively greater degree of complex movement control by females, particularly when traversing the zigzag rod (Kucinski et al. 2018; Kucinski et al. 2019). Moreover, our prior study on the effects of TAK-071 on sustained attention performance in rats with BF cholinergic lesions indicated a broader efficacy of the compound in females (Kucinski et al. 2020). Although there is evidence indicating that female humans likewise exert relatively superior cognitive control of complex movements (Pereira et al. 2013; Hollman et al. 2011; Lissek et al. 2007), these effects of sex in rats may primarily inform about effects of neuronal and pharmacological manipulations in interactions with biological variations of complex movement control.
The fall-reducing effect of the lower dose of TAK-071 on rotating straight rod traversal in DL rats was associated with a nonsignificant decrease in traversal speed when compared with DL-V rats (Fig. 2c). Moreover, and mirroring sham-operated, non-treated rats (S-V), a significant correlation between traversal speed and fall rate was found. In contrast, these two measures were not correlated in DL rats treated with the higher dose of TAK-071, that is, in DL-0.3 rats a trend for a decrease in falls was not associated with relatively faster traversal speed (see the “flatter” regression line for DL-0.3 rats in Fig. 2d). As is the case in older humans and PD patients (Holtzer et al. 2014; Coelho et al. 2012; Plotnik et al. 2011; Springer et al. 2006), our collective evidence suggests that in rats, slower traversal or gait speed reflects limitations in the attentional control of movement, rather than an impairment in “purely” motor functions. The conclusion that the lower dose of TAK-071 acted primarily by restoring the top-down control of movement, perhaps by benefiting the (residual) ability of DL rats to process task- and proprioceptive cues, is consistent with the efficacy of this dose on the attention of rats with solely cholinergic losses (Kucinski et al. 2020).
In contrast to fall rates on straight rotating rod, fall rates from the rotating zigzag rod benefited from both doses of TAK-071. Traversing this rod, with the direction of rotation alternating from trial to trial, arguably taxes gait and balance control robustly more than the straight rotating rod. Moreover, falls across all experimental groups differentiated specifically when the angled part was at a steep angle upon entering (Fig. 3b). At a “flatter” angle (as illustrated in Fig. 1b), rats appeared to be able to maintain a seemingly regular paw placement rhythm and a stable patterning of movement while traversing the zigzag segment. At a steep angle, and presumably triggered by mismatches between habitually pre-programmed movement sequences and the balancing and stepping demands of walking up or down at a steep and rapidly changing angle (30°/s), such patterning may have been disrupted. Upon entering a steep-angled part, rats often displayed a momentarily “slouched” position, perhaps indicating such disruption of stable movement pattern. Thus, performance on the steep angle condition of the zigzag may serve as a particularly robust indicator of the ability to revise the movement plan and, compared to more flat positions of the zigzag or traversing the rotating straight rod, to integrate information about dynamic surfaces, posture, and balance with ongoing gait. In other words, the steep zigzag condition may potently trigger a robust attentional shift toward movement (re)programming (see also Wong et al. 2015).
The reduction of falls from the zigzag rod seen in DL rats treated with TAK-071 was observed on the second, but not the first, day of testing this rod when rotating in alternating direction from trial to trial (that is, on day 7, but not day 6, on Table 1). This finding suggests that the effects of the drug treatment on day 7 depended on practicing traversal of prior rod conditions in the presence of drug. Although potential interactions between the present treatment regimen and the escalating demands imposed by the changing task conditions (Table 1) complicate the interpretation of behavioral effects, such interactions reflect that treatments which enhance behavioral functions, or even rescue behavioral deficits, are unlikely to install instant, “magic bullet”-like, improvements in behavior. Rather, such treatments would be assumed to act via progressively influencing the bidirectional interplay between neuronal activity and behavior (Sarter 2006).
Although great caution is warranted when using the present, relatively limited data set from rats to predict clinical efficacy of the compound, the current findings as well as the prior results indicating a pro-attentional efficacy of TAK-071 (Kucinski et al. 2020) suggest that the demonstration of efficacy of TAK-071 is a function of the demands on attentional control of complex movements. It would appear less likely that this treatment benefits primarily motor parameters of gait and balance. Dual task testing situations, which have often been employed to reveal gait and balance disorders and fall risks in aged persons and PD patients (e.g., Yogev-Seligmann et al. 2008, 2012, 2013; Springer et al. 2006; Mersmann et al. 2013; Woollacott and Shumway-Cook 2002; Shumway-Cook et al. 1997; Plotnik et al. 2011), or other manipulations which strongly tax the attentional control of gait, may be crucial for demonstrating pharmacological efficacy. Finally, the present findings suggest that repeated behavioral testing in the presence of the treatment may reveal the progressively beneficial modulation of cognitive-motor interactions by this M1 PAM.
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Acknowledgements
We thank Dr. Arthur Simen (Takeda, Cambridge, MA) for comments on a draft of this manuscript.
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AK conducted the experiments and analyzed the data. AK and MS wrote the paper.
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The research described in this manuscript was supported by NIH grant P50NS091856 (Morris K. Udall Center for Excellence in Parkinson’s Disease Research). TAK-071 was obtained from Takeda Pharmaceutical Company. Dr. Sarter previously received compensation as a consultant for Takeda (2017-2019). No such consulting activity took place during the period this research was conducted (2020).
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Kucinski, A., Sarter, M. Reduction of falls in a rat model of PD falls by the M1 PAM TAK-071. Psychopharmacology 238, 1953–1964 (2021). https://doi.org/10.1007/s00213-021-05822-x
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DOI: https://doi.org/10.1007/s00213-021-05822-x