As serotoninergic transmission plays a crucial role in higher brain function in mammals, the disturbance of this system will likely have significant effects on emotion and cognition. Previous studies have reported that chronic treatment with Specific Serotonin Reuptake Inhibitors (SSRIs) during both late pregnancy and lactation was associated with abnormal behavior in adult rats. These data imply that disturbances in serotoninergic transmission during neurodevelopment may have negative effects on both the structure and function of the resultant adult brain. Therefore, the effect of a single exposure to an SSRI or a tricyclic antidepressant that preferentially inhibits serotonin reuptake during the pre-weaning period was examined in adult mice. An oral infusion of paroxetine (70 mg/kg), fluvoxamine (250 mg/kg), clomipramine (180 mg/kg), or saline was administered on postnatal day 14. Starting at 11 weeks of age, mice were assessed using a comprehensive behavioral test battery. Mice treated with paroxetine demonstrated altered behavior on the open field and hole-board tasks; those treated with fluvoxamine had behavioral changes on the light-dark box, hole-board, and sucrose preference tasks, while alteration in forced swimming and cued fear behavior were noted in mice treated with clomipramine. These results suggest that even a single administration of an antidepressant could have profound effects on behavior in adulthood, although the effects might differ dependent on the specific drug that was administered.
Specific Serotonin Reuptake Inhibitors (SSRIs) are generally known to be effective with a relatively low risk of adverse events in the treatment of depression or obsessive-compulsive disorder during pregnancy and lactation [
Some studies have reported that exposure to paroxetine in utero might lead to perinatal complications, including premature parturition [
Furthermore, recent studies have suggested that behavioral changes induced by neonatal SSRI exposure might contribute to long-lasting changes in the nervous system. For instance, modification of 5-HT abundance in the brain during embryonic development in mice disrupted the precision of sensory maps formed by thalamocortical axons [
Some studies have reported that a single exposure to drugs during pregnancy and/or the neonatal period was sufficient to induce developmental and/or behavioral effects [
The present study examines three aims. The first is to assess the delayed behavioral influence of disturbances in serotoninergic transmission induced by antidepressants on a comprehensive behavioral battery. Second, we examine how a single excessive exposure of several types of antidepressant during development may influence behavior in adulthood. Finally, we compare antidepressants to characterize the unique effect of each on behavioral responding in adult mice.
Forty-nine (paroxetine exposure experiment), thirty-nine (fluvoxamine exposure experiment), and fifty-eight (clomipramine exposure experiment) male C57BL/6J mice were used in this study. Mice were obtained by the mating of commercially obtained male and female C57BL/6J mice (JCL, Tokyo, Japan). All mice were weaned at 4 weeks of age and then housed 3 to 4 animals of littermates per cage. At 10 weeks of age, mice were individually housed for 1 week prior to behavioral testing. The breeding and experimental rooms were air-conditioned (22˚C, 50% - 60% humidity) and a 12-h light-dark cycle was implemented (lights on at 0800). Food and water were freely available in their home cages. All behavioral assessments except home cage activity monitoring and social interaction test were conducted during the light cycle between 1300 and 1700. All procedures were performed in strict accordance with the guidelines of the Institute of Physical and Chemical Research (RIKEN) and were approved by the institute’s Animal Investigation Committee.
Paroxetine hydrochloride (LKT Laboratories, MN, USA; 70 mg/kg), fluvoxamine maleate (TRC, Ontario, Canada; 250 mg/kg), and clomipramine hydrochloride (SIGMA, MO, USA; 180 mg/kg) were used in this study. All drugs were dissolved at room temperature in physiological saline before behavioral testing. The selected doses were determined by previously conducted pilot experiments to determine safe and efficacious doses of each of the experimental treatments. On postnatal day 14, each animal was administered either the drug or saline orally (per os; P.O.) through a stainless-steel cannula (Muromachi-kikai, Tokyo, Japan) (10 µl/g body weight).
At the age of 11 weeks, behavioral testing began. A three-stage behavioral test battery was used in this study (
Home cage activity measurement: Spontaneous home cage activity of mice was measured using a 24-channel activity measurement system (O’Hara, Tokyo, Japan). Cages were individually placed into compartments made of stainless steel in the negative breeding rack (JCL, Tokyo, Japan). A piezoelectric sensor was equipped on the ceiling of each compartment and detected mouse movement (4 to 5 times per s). Home cage activity was measured 24 h for one week beginning in the afternoon on the day of transferring to the behavioral laboratory and daily for the next week. After the completion of home cage activity assessment, cages and bedding materials were changed and mice were then maintained throughout behavioral screening in a micro-isolation rack (Allentown, NJ, US) identical to those used in the breeding rooms.
Open field test: A four-channel open field system was equipped in a small soundproof room (185 × 185 × 225 cm (H)). Each field was made of white plastic (50 × 50 × 40 (H) cm) and illuminated by LEDs (70 Lux at the center of the field). Behavior was monitored by a charge-coupled device (CCD) camera equipped on the ceiling of the rack for the open field. During testing, the soundproof room was dark and an electronic fan was running both for ventilation and background noise (35 dB). In the open field test, each mouse was placed in the center of the field and allowed to move freely for 15 min. Distance traveled (cm) and time (s) spent in the center area of the field (36% of the center of the overall field) were adopted as indices. Data were collected every minute and analyzed using Image J OF4 (O’Hara, Tokyo, Japan).
Light-Dark (LD) box test: A four-channel light-dark box system was equipped in the aforementioned soundproof room. Each light box was made of white plastic (20 × 20 × 20 cm (H)) and illuminated by LEDs (250 Lux at the center of the box) with a CCD camera equipped on the ceiling. Each dark box was made of
Behavioral task | Behavioral properties to assess | Ref. No. |
---|---|---|
Battery 1: | ||
Home cage activity | Spontaneous activity | [ |
Open field test | Locomotor activity, anxiety (induced by novelty) | [ |
Light-dark box test | Locomotor activity, anxiety (induced by brightness), conflict | [ |
Elevated plus maze test | Locomotor activity, anxiety (induced by height), conflict | [ |
Auditory startle response (and prepulse inhibition) | Hearing ability, auditory information processing | [ |
Barnes maze test | Spatial memory | [ |
Classical fear conditioning | Memory of fear event (both spatial and cued memory) | [ |
Battery 2: | ||
Hole board test | Exploration (curiosity) | [ |
Social interaction | Affiliative behavior | [ |
Hot plate test | Pain sensation (central) | [ |
Tail flick test | Pain sensation (peripheral) | [ |
Forced swimming test | Behavioral despair (depression) | [ |
Tail suspension test | Behavioral despair (depression) | [ |
Battery 3: | ||
Elevated zero maze test | Locomotor activity, anxiety (induced by height), conflict | [ |
Stair case test | Anxiety (induced by novelty), impulsiveness | [ |
Marble burying test | Compulsiveness | [ |
Sucrose preference test | Behavioral despair (depression) | [ |
Restraint stress test (blood glucose measurement) | Stress vulnerability | [ |
black plastic (20 × 20 × 20 cm (H)) with an infrared camera equipped on the ceiling. There was a tunnel with a sliding door in the center panel for transition between the light and dark boxes (3 × 5 cm). In the LD box test, mice were individually introduced into the light box. The door to the tunnel automatically opened when the software detected the introduction of a mouse to the testing arena. Mice were then allowed to move freely in the LD box for 10 min. Total distance traveled, percent distance traveled in the light box, percent time spent in the light box, number of the transitions between light and dark box, and the latency to first enter the dark box were measured on this task. Data were collected every minute and analyzed using Image J LD4 (O’Hara, Tokyo, Japan).
Elevated plus maze test: A single-channel elevated plus maze (closed arms: 25 × 5 × 15 cm (H); open arms 25 × 5 × 0.3 cm (H)) was equipped in the aforementioned soundproof room. The floor of each arm was made of white plastic while the wall of each closed arm and ridge of each open arm were made of clear plastic. Closed and open arms were arranged orthogonally 60 cm above the floor. Lighting during testing was 70 Lux at the center platform of the maze (5 × 5 cm). In the elevated plus maze test, mice were individually placed on the center platform facing an open arm and were then allowed to move freely in the maze for 5 min. Total distance traveled, percent time spent in the open arms, and percent open arm entries were measured on this task. Data were collected every minute and analyzed using Image J EPM (O’Hara, Tokyo, Japan).
Auditory startle response and prepulse inhibition test: The auditory startle response test was conducted in a soundproof room as previously described [
Barnes maze test: For a spatial learning and memory task, we used the Barnes maze test. On the first day, a habituation trial was conducted. On this trial, mice were individually placed at the center of the maze and allowed to explore freely for 5 min. Following habituation, escape training commenced. During this training, mice were individually placed in the center of the maze and led to an escape hole. Mice were then encouraged to escape into one of the 12 holes on the maze (by softly pinching the animal’s tail, if needed). This was repeated 5 times, changing the position of the escape hole on each trial. Maze training was conducted three times a day for four days. During training, mice were placed into a small plastic container at the center of the maze for 10 s. The container was then opened to begin the trial. Each trial terminated when the mouse escaped into the correct hole (escape cage) or 120 s had elapsed. Mice were left in the escape cage for 30 s and then returned to their home cage. The inter-trial interval was approximately 15 min. A probe test was conducted after the final maze training session on the fifth day. The probe test was identical to maze training, except that no escape cage was provided. The apparatuses and software used are commercially available (Image J BM; O’Hara, Tokyo, Japan).
Classical fear conditioning: The classical fear conditioning test consisted of three parts: a conditioning trial (Day 1), a context test trial (Day 2), and a cued test trial (Day 3). Fear conditioning was carried out in a clear plastic chamber equipped with a stainless steel grid floor (34 × 26 × 30 cm (H)). A CCD camera was equipped on the ceiling of the chamber and was connected to a video monitor and computer. The grid floor was wired to a shock generator. White noise (65 dB) was supplied from a loudspeaker as an auditory cue (CS). The conditioning trial consisted of a 2 min exploration period followed by two CS-US pairings separated by a minute each. A US (foot shock: 0.5 mA, 2 s) was administered at the end of the 30-s CS period. A context test was performed in the same conditioning chamber for three minutes in the absence of the white noise CS 24 h after the conditioning trial. Further, a cued test was performed in an alternative context with distinct cues: the testing chamber was different from the conditioning chamber in brightness (almost 0 - 1 Lux), color (white), floor structure (no grid) with bedding on the floor (alpha-dri, Shepherd, TN, USA), and shape (triangular). The cued test was conducted 24 h after the contextual test was completed. The cued test consisted of a 2-min exploration period (no CS) to evaluate nonspecific contextual fear followed by a 2-min CS period (no foot shock) to evaluate the cued fear. Frequency of the freezing response, characterized as immobility other than respiration and heartbeat, was measured as an index of fear memory in these mice. Data were collected and analyzed using Image J FZ2 (O’Hara, Tokyo, Japan).
Hole board test: An open field arena made of gray plastic (50 × 50 × 40 cm (H)) with four equally-spaced holes (3 cm in diameter with an infrared sensor) on its floor was used (Model ST-1/WII, Muromachi-kikai, Tokyo, Japan). The field was illuminated by fluorescent light (180 Lux at the center of the field) and background noise was approximately 50 dB. The behavior of each mouse was monitored by a CCD camera suspended about 1.5 m above the field. In the hole board test, mice were individually introduced into the center of the field and allowed to explore freely for 5 min. Distance traveled (cm), latency for head dipping (s), number of head dipping, duration of head dipping (s), duration of rearing (s), and the number of rearing events were measured on this task. Data were collected and analyzed using the CompACT VAS system (Muromachi-Kikai, Tokyo, Japan).
Social interaction test (encounter method): Mice were individually put into the center of a white-colored open field (40 × 40 × 30 cm (H)) with thin bedding material (alpha-dri, Shephard, TN, USA). Immediately after the introduction of the subject mouse, a target mouse (C57BL/6J, JCL, Tokyo, Japan) was introduced into the same open field arena. The duration of contact behavior was measured for 6 h. Contact or separation of mice was expressed as a “1” or “2,” respectively, with a sampling time of 0.5 s. If the two mice contacted one another, the software returned a value of “1” and if separated, returned a value of “2.” Data were collected and analyzed using a computer and commercially available software (Time HC: O’Hara, Tokyo, Japan).
Hot plate and tail flick test: In the hot plate test, mice were individually placed on the plate (Model MK-350C, Muromachi-kikai, Tokyo, Japan; 52˚C ± 0.5˚C) enclosed by a translucent plastic wall. The time between placement and a flinch of the hind paws, licking of fore paws, and jumping was recorded manually. The maximum trial length was 90 s for each animal. In the tail-flick test (Model MK-330B, Muromachi-kikai, Tokyo, Japan), mice were individually restricted to the radiant heat meter, and focused heat was applied to the surface of the tail 2 - 3 cm from the tip. The latency to reflexive removal from the heat was recorded manually as the tail flick latency. The maximum testing time was 10 s for each animal. On each of these tests, times were recorded by two observers and the shortest latency between them on each trial was used as the response time.
Forced swimming test: Mice were individually placed in a glass cylinder (30 cm high, 10 cm in diameter) filled 10 cm from the bottom with water maintained at 23˚C - 25˚C for 15 min. The duration of immobility was scored and analyzed using Image J TS (O’Hara, Tokyo, Japan).
Tail suspension test: Mice were individually hung by the tail using adhesive tape placed approximately 1.5 cm from the tip of the tail attached to a wire and 30 cm above the floor. The duration of immobility during the 5-min testing session was scored and analyzed using Image J TS (O’Hara, Tokyo, Japan).
Elevated zero maze test: A zero maze (O’Hara, Tokyo, Japan; 40 cm diameter, 5 cm width) that consisted of two enclosed areas and two open areas was hung 50 cm above the floor in a soundproof room. Mice were placed in the closed part of the maze and allowed to explore freely for 5 min with a luminescence of 70 Lux. Total distance (cm), percent time (sec) spent in the open areas, and percent entries into the open areas were measured as indices of performance. Data were collected and analyzed using Image J OF (O’Hara, Tokyo, Japan).
Staircase test: We used the staircase test as an additional task to assess anxiety and impulsiveness. The staircase apparatus consisted of a clear plastic enclosure (Brain Science Idea, Osaka, Japan; 10 × 45 × 15 cm (H)) with five identical steps made of white plastic (7.5 cm × 10 cm × 2.5 cm on top of each step). The box was placed in a room with constant lighting (300 Lux) and background noise (50 dB). Each animal was placed on the bottom floor of the staircase. The latency to reach the top (sec), the number of stairs climbed, and the number of rearing events was recorded during a 3-min period. Climbing was defined as each stair on which the mouse placed all four paws, and rearing was defined as each instance the mouse rose up on hind legs either on a stair or by leaning against the wall. The number of stairs descended was not taken into account.
Marble burying test: The marble burying test was conducted as previously described [
Sucrose test: Mice were tested for 3 days on the 24-h version of the task, and 1 day for the 1-hr version of the task with 24-h of water deprivation. 24-h tests were a free choice between two bottles, where one bottle was filled with 3% sucrose in filtered water and the other only filtered water. To counterbalance bias for a preference to side, the position of bottles were switched every 24 h. The consumption of the water or sucrose solution was assessed daily. After the last 24-h choice test, mice were deprived of water for 24 h and then the 1-h choice test between water and sucrose was conducted.
Blood glucose concentration measurement: Each mouse had their blood glucose concentration assessed three times: just before restraint stress exposure in a tight wire-mesh cage (30 min; Shinano, Tokyo, Japan), just after restraint stress exposure, and 90 min after the termination of stress exposure. Blood concentration was measured by the CareFast blood glucose sensor (Nipro, Tokyo, Japan). For each measurement, tails were cut and a small amount of blood (5 µl) was collected into a disposable sensor.
Statistical analyses were conducted using the SPSS™ 19 statistical package (Japan IBM, Tokyo, Japan). Student’s t-test was used to compare the two groups on continuous data and the Mann-Whitney’s U-test was used to analyze ratio data. Repeated testing paradigms were analyzed using repeated measures ANOVA (general linear model; GLM). When Mauchly’s hypothesis of sphericity was not supported, the degrees of freedom were modified using the Greenhouse-Geisser method [
Results of the three stages of behavioral test battery are summarized in
Paroxetine-exposed mice exhibited behavioral changes in the open field and the hole-board test. In the open field test, locomotor activity of paroxetine-exposed mice was decreased relative to control mice, although this difference was not significant (
Behavioral task/indices | Paroxetine | Fluvoxamine | Clomipramine | ||
---|---|---|---|---|---|
Battery 1: | |||||
Sample size (drug/saline) | 7/8 | 7/10 | 8/10 | ||
Body weight | ns | ns | ns | ||
Home cage activity | ns | ns | ns | ||
Open field test | |||||
Distance traveled | ns | ns | ns | ||
Time center | ↓ | ns | ns | ||
Light-dark box test | |||||
Distance traveled | ns | ns | ns | ||
%Distance light | ns | ↓ | ns | ||
%Time light | ns | ↓ (trend) | ns | ||
No. of transition | ns | ns | ns | ||
First latency to enter dark | ns | ns | ns | ||
Elevated plus maze test | |||||
Distance traveled | ns | ns | ns | ||
%Time open | ns | ns | ns | ||
%Number open | ns | ns | ns | ||
Auditory startle response (and prepulse inhibition: PPI) | |||||
Startle response | ns | ns | ns | ||
Startle threshold | ns | ns | ns | ||
PPI | ns | ns | ns | ||
Barnes maze test | |||||
Distance traveled | ns | ns | ns | ||
Latency to enter | ns | ns | ns | ||
No. of error | ns | ns | ns | ||
Probe test | ns | ns | ns | ||
Classical fear conditioning (freezing) | |||||
Conditioning | ns | ns | ns | ||
Context test | ns | ns | ns | ||
Cued test | ns | ns | ↓ | ||
Battery 2: | |||||
Sample size (drug/saline) | 9/10 | 4/6 | 10/10 | ||
Hole board test | |||||
Distance traveled | ↓ | ↓ | ns | ||
Latency for head dipping | ↑ | ns | ns | ||
Number of head dipping | ns | ns | ns | ||
Duration for head dipping | ns | ns | ns | ||
Duration of rearing | ns | ns | ns | ||
Number of rearing | ns | ns | ns | ||
Social interaction | ns | ↓ (partially) | ↑ |
---|---|---|---|
Tail flick test | ns | ns | ns |
Hot plate test | |||
Latency of locking | ns | ns | ns |
Latency of flinch | ns | ns | ns |
Latency of jumping | ns | ns | ns |
Forced swimming test | ns | ns | ↓ |
Tail suspension test | ns | ns | ns |
Battery 3: | |||
Sample size (drug/saline) | 6/9 | 6/6 | 10/10 |
Elevated zero maze test | |||
Distance traveled | ↓ (partially) | ↑ | ns |
Latency to enter open | ns | ↓ (trend) | ns |
%Time open | ns | ↓ (trend) | ns |
%Number open | ns | ns | ns |
Stair case test | |||
Latency to reach the top | ns | ↓ | ns |
No. of step ascend | ns | ns | ns |
No. of rearing | ns | ns | ns |
Marble burying test | ns | ns | ns |
Sucrose preference test | |||
Training (consumption) | ns | ns | ns |
Preference test (vs water) | ns | ↓ | ns |
Restraint stress test (blood glucose measurement) | |||
Baseline | ns | ns | ns |
Immediate after the stress | ↓ | ns | ns |
90 min after the stress | ns | ns | ns |
Contrary to the paroxetine-exposed mice, fluvoxamine-exposed mice demonstrated no differences on open field test, but exhibited some inconsistent behavioral changes among the anxiety-and depression-related tasks. In the LD box test, the percent distance traveled in the light box among fluvoxamine-exposed mice was significantly lower than that of the control mice [U (15) = 57, p = 0.032;
Although fluvoxamine-exposed mice exhibited increased anxious responding on the LD box test, they did not show any differences in the elevated plus maze test. In the elevated zero maze test, fluvoxamine-exposed mice spent proportionally less time in the open area [U (8) = 3, p = 0.055;
In the forced swimming test, mice exposed to clomipramine showed a significant main effect of drug treatment [F (1, 18) = 9.151, p = 0.007] and time bin [F (5.377, 96.784) = 37.989, p < 0.001], but the interaction between drug treatment and time bin was not significant [F (5.377, 96.784) = 0.916, p = 0.479]. Mean immobility rate was also statistically significant [whole test: U (18) = 13, p = 0.005, data not shown; bin 1 to 5: U (18) = 16, p = 0.01,
Furthermore, clomipramine-exposed mice exhibited a slight but statistically significant impairment in cued memory on the fear conditioning test (
In the present study, we demonstrated that among infant mice, a single exposure to antidepressants might affect
their emotional behavior in adulthood. Paroxetine-exposed mice had less reactivity to the novel environment (e.g., decreased time spent in the center of the open field arena, decreased distance traveled, increased head dip latency on the hole board test, and decreased response to the restraint stress;
Effects of exposure to antidepressants in utero and during lactation have been studied in both humans and animals. Clinical studies revealed that exposure to antidepressants during pregnancy may cause physical problems in the newborn (e.g. hypertension, low body weight) [
after exposure to antidepressants via breast milk, most studies have focused on the pharmacokinetics of antidepressants in breast-feeding. Thus, the long-term effects of exposure to antidepressants during neurodevelopment on behaviors in adulthood are still unknown [
NADES posits two fundamental questions in this field of research. The first is whether antidepressant exposure in utero affects neurodevelopment and behavior. The second is whether functional changes caused by antidepressant exposure in utero or during lactation are associated with structural changes. Animal research thus far strongly suggests that antidepressant exposure in utero may affect neurodevelopment and subsequent adult behavior. However, few longitudinal clinical studies of this nature exist [
In contrast to previous studies that chronically exposed animals to drugs, this study used a single excessive exposure to a variety of antidepressants. Therefore, the mechanisms that mediate behavioral change in this study may differ from those of previous studies because of this methodological discrepancy. However, a single disturbance in glutamatergic [
I would like to thank Drs. Kanno J. and Kitajima S. at National Institute of Health Sciences and Professor Tanemura K. at Tohoku University for inviting me to work on this research project in developmental and behavioral toxicology. I would also like to thank Ms. Homma C. for her technical assistance. This study was in part supported by Health Sciences Research Grants from the Ministry of Health, Labour, and Welfare, Japan (FY 2008-2010).
Kazuyuki Yamada, (2016) Single Exposure to Antidepressants during Infancy Is Associated with Delayed Behavioral Changes in C57BL/6 Mice. World Journal of Neuroscience,06,151-164. doi: 10.4236/wjns.2016.62019