Background
Depression is a complex psychiatric disorder characterized by anhedonia and feelings of sadness [
1]. It is not only life threatening but also has a negative impact on cognitive processes, especially learning and memory [
2]. Stress is known to be a key factor in the development of depression and memory impairment. However, the pathogenes of stress leading to depression and its effective therapeutic strategies have not been clearly identified.
There are many limitations in conducting research on the etiology of depression and the efficacy of new drugs on individuals with depression due to ethical reasons. Therefore, it is imperative to use reliable preclinical animal models in order to evaluate effective therapies prior to implementing these strategies in the clinic. One rat model of depression, which was initially described by Willner [
3], uses a regimen of chronic unpredictable mild stress (CUMS) to mimic the daily hassles and stress levels in humans. It has been commonly used to study the etiology of depression and antidepressant efficacy [
4,
5].
Resting-state functional magnetic resonance imaging (r-fMRI), a promising neuroimaging technique that measures intrinsic or spontaneous neural activity in vivo [
6], has been increasingly used to study neuropsychiatric disorders, including mild cognitive impairment (MCI) [
7], depression [
8], Alzheimer’s disease (AD) [
9], schizophrenia [
10] and medial temporal lobe epilepsy [
11]. In contrast to task-based experimental paradigms, r-fMRI is another way to capture brain activity from rodents that are unable to complete functional tasks due to the anesthesia and/or restraint used during traditional fMRI data acquisition [
12]. Analysis of the amplitude of the low-frequency fluctuations (ALFF) and the regional homogeneity (ReHo) are two methods that investigate the resting-state activity in regions across the brain [
13,
14]. These two methods have been successfully applied to detect alterations in subjects with various mental disorders [
7,
8,
15,
16]. ALFF measures the amplitude of the regional spontaneous neuronal activity [
17]. The ReHo method, developed by Zang et al. [
14], focuses on the similarities or the coherence of intraregional spontaneous low-frequency activity, measuring the level of coordination in regional neural activity. Hence, ALFF and ReHo, which provide different types of information regarding neuronal activity, are two complementary methods that investigate alterations in the activity of the entire brain. The combination of ALFF and ReHo may provide a more comprehensive pathophysiological assessment of brain dysfunction than either method alone, especially in exploratory research.
Angiotensin type 1 receptor (AT1 receptor) blockers have attracted much attention for their possible antidepressant effects. The renin-angiotensin system (RAS) is one of the critical body reaction systems in response to stress [
18]. The pathophysiological response to stressful stimuli that exceeds the body’s adaptive mechanisms include increased brain Angiotensin II (Ang II) activity, amplified AT1 receptor expression, which is associated with higher hypothalamic-pituitary-adrenal (HPA) axis activation, and enhanced peripheral RAS activity [
19]. In addition, excessive brain AT1 receptor activity is associated with brain inflammation [
20], which is involved in the pathogenesis of emotional and cognitive impairments [
21]. Telmisartan, a commonly used angiotensin receptor blockers (ARBs), is very lipophilic, which allows it to readily cross the brain-blood barrier (BBB). Because telmisartan induces central AT1 receptor blockade [
22], this compound can be used as a potential oral antidepressant. Several studies have demonstrated that telmisartan is neuroprotective [
23] and can attenuate cognitive impairments induced by chronic stress in rats [
24]. However, there are few reports to explore which brain regions telmisartan’s possible antidepressant effect is related to.
Based on the previous reports, we hypothesized that telmisartan could alleviate the depressive and cognitive dysfunction symptoms caused by chronic stress. The related brain regions could be explored by the ALFF and Reho analysis for r-fMRI. Hence, we employed the two analyses to directly compare the resting-state brain activity among normal rats, rats that were exposed to chronic stress, and rats exposed to chronic stress and administered telmisartan. In addition, the open field test (OFT), the sucrose preference test (SPT), and the object recognition test (ORT) were conducted to evaluate locomotor activity, anhedonia, and cognition in the experimental animals.
Methods
Animals
These experiments were conducted in male Sprague-Dawley rats (5 weeks), provided by Beijing Weitong Lihua Experimental Animal Technology Co., Ltd. (experimental animal production license: SCXK Beijing 2012–0001). The rats were housed 4 per cage in a temperature-(18–24 °C) and humidity-(40–60%) controlled room on a 12 h light/dark cycle (lights on at 7:00 a.m.). The rats had free access to standard laboratory food and tap water. Animal maintenance was performed according to the National Institutes of Health Guidelines for the Care and Use of Laboratory animals [
25].The experimental protocols were approved by the Beijing University of Chinese Medicine Institutional Animal Care and Use Committee (Ethics number: 2013BZHYLL1001B). All efforts were made to minimize animal suffering. All animals were decapitated after anesthetized deeply with isoflurane.
Drug administration and experimental groups
After 2 weeks of acclimation, 32 rats were randomly divided into 4 groups with 8 animals per group including: (1) a Control group (C group)that was administered distilled water as a vehicle; (2) a Stress group (S group)that underwent the CUMS procedure and was administered distilled water; (3) a Stress + Telmisartan group (T-0.5 mg/kg group) that underwent the CUMS procedure and was administered telmisartan (0.5 mg/kg) dissolved in distilled water; (4) a Stress + Telmisartan group (T-1 mg/kg group) that underwent the CUMS procedure and was administered telmisartan (1 mg/kg) dissolved in distilled water. The telmisartan dose of 1 mg/kg is considered to be a nonhypotensive dose in rats [
26,
27]. The rats received either telmisartan or vehicle by oral gavage each day immediately before the stress procedure.
Chronic unpredictable mild stress (CUMS) procedures
The rats in the C group were housed in groups of 4, while the rats in the S and T groups were singly housed in isolation. The following stimulations were applied to the experimental animals, according to previous CUMS rat model methods. These included 12 h food deprivation, 12 h water deprivation, overnight wet housing, forced swimming (4 °C for 5 min), 2.5 h restraint, overnight illumination, 45°cage tilt for 12 h, and 36 sessions of inescapable foot shock (1.5 mA intensity; 30 shocks in 1 min, with an inter-session interval of 30s). The rats were exposed to a random selection of 2 stressors per day, with no repetition of the same type on continuous days, in order to have the stimulation remain unpredictable. The CUMS process lasted for 4 continuous weeks. The behavioral experimental tests were performed 24 h after the last stimulation. There were no rats injured or ill during the experiment.
Open field test (OFT)
The open field test was performed to assess the rats’ spontaneous exploratory activity. The open field arena was a square 100 cm × 100 cm black floor divided by 8 lines into 25 equal squares, surrounded by a 35 cm high wall. A digital camera was placed 2 m above the open field to capture the whole field. During OFT, the rats were placed in the center of the field and recorded using a small animal behavior recorder for 3 min. The rearings were counted manually during the recording. An animal behavior analysis system was used to analyze the total moved distance during the 3 min.
Sucrose preference test (SPT)
The sucrose preference test evaluated potential anhedonia in the experimental animals. The rats were trained for the SPT by providing a continuous choice of 2 bottles, which contain 2% sucrose, for 24 h. Afterwards, one of the bottles was replaced with water for 24 h. During this 24-h period, the bottles were switched after 12 h to control for any side bias. Following this adaptation procedure, the rats were deprived of water and food for 12 h. The SPT was conducted at 9:00 a.m. The rats were housed in individual cages and given free access to the 2 bottles of water and sucrose, which were weighed in advance. After 4 h, the weight of both the consumed sucrose solution and water was recorded. The sucrose preference was calculated as sucrose preference (%) = sucrose consumption (g)/(sucrose consumption (g) + water consumption (g)) × 100%.
Object recognition test (ORT)
Object recognition was evaluated in a plastic box 62 cm long, 40 cm wide and 45 cm high. The objects, which were in duplicate, were made of glass, and did not appear to have any innate significance for the subject animals. The rats were naïve to the objects, which were weighted so they could not be displaced by the test subject. ORT was performed as described previously [
28]. Briefly, all rats underwent 2 habituation sessions with a 1 h inter-session interval. During habituation, the animals were allowed to freely explore the apparatus for 3 min. After 24 h, the rats returned to the testing apparatus for the experimental session. The experimental session consisted of 2 trials, which were 3 min and 5 min in duration, respectively. During the first trial (T1), the rats were exposed to 2 identical objects, A1 and A2. During the second trial (T2) 60 min later, the rats were exposed to 2 objects, a duplicate of either A1 or A2, and a new object, B. The position of the 2 objects was counter balanced and randomly permuted during T2 in order to reduce any bias due to object and place preference. Object recognition was assessed by the subject rat’s T2 object exploration time. The object exploration was defined as the subject touching the object with its nose. Turning around or sitting on the object was not considered to be exploratory behavior. The time spent in exploring the 2 different objects in T2 was recorded. Object recognition was defined as variable B-A, and B-A/B + A.
fMRI acquisition
fMRI measurements were conducted on a 7.0 T /16US MRI scanner (Bruker), using a radiofrequency transmission coil (300 1H 089/072 QUAD TO AD) and a 38 mm rat head surface coil for receiving. The rats were anesthetized with isoflurane/O2 (5% for induction and 1–1.5% for maintenance) and prostrated on a custom-made holder to minimize any head motion. The respiration was monitored at a rate of 40–50 breaths per min. First, the T2-weighted data were acquired for the localization of the functional scans. Then, the resting-state functional images were recorded axially over 13 min and 26 s with the following parameters: repetition time (TR) = 3280 ms, Matrix = 128*128, echo time (TE) = 27.6 ms, flip angle = 90°, 20slices ,thickness/gap = 1.0 mm/0.2 mm, field of vision (FOV) =2.5 cm × 2.0 cm.
Discussion
The present study investigated the behavioral and cerebral alterations induced by chronic stress and telmisartan administration. To the best of our knowledge, this is the first study using ALFF and ReHo methods in a rat model of depression to examine whole brain r-fMRI alterations caused by stress and telmisartan administration.
According to our behavioral results, chronic stress decreased locomotor activity, sucrose preference and impaired ability of novel object recognition, which is in line with the results of previous studies, and suggests that we successfully established a rat model of depression [
24,
32]. Since the dose of 1 mg/kg/day telmisartan has been proven nonhypotensive for mice [
26], we applied two doses’ (1 mg/kg/day and a lower dose, 0.5 mg/kg/day) telmisartan on the model. We found that the telmisartan of 1 mg/kg /day could significantly improve the impaired ability of novel object recognition, while the effect of 0.5 mg/kg/day was weak. Since the ORT indicating a kind of cognitive function, it’s worth conducting additional experiments such as Morris water maze to evaluate telmisartan’s potential effect on the cognitive function more comprehensively. For the tests of OFT and SPT, we found a trend for telmisartan to improve the decreased locomotor activity and sucrose preference, although these were not significant. A previous study showed that the treatment with telmisartan of 1 mg/kg for five weeks could notably improve the depressive symptoms in the stress mouse model [
33]. Hence, the not significant effect may be due to the short treatment time and a relatively small dose for rats. Taken together, these data demonstrated a possible antidepressant effect with telmisartan. It’s worth performing further analyses to look into the potential of telmisartan in alleviation of symptoms of depression.
We observed no significant alterations in ALFF in the chronically stressed rat compared to the normal rat. However, there were widespread cerebral region alterations in ReHo between the two groups. To some extent, it can be concluded that the coordination of regional neural activity, rather than its amplitude, may be more easily disrupted by chronic stress.
In the present study, we observed that the rats in the S group had increased ReHo in some limbic system regions, including the hippocampus, hypothalamus,thalamus, and olfactory cortex. The hippocampus, a critical structure in the limbic system, is well-known for its important role in the formation of depression [
34] and cognitive decline [
35]. The result of increased ReHo value in the hippocampus is consistent with a previous study on the later adult onset depression patients, supporting the validity of our findings [
36]. There were rare clinical reports about the altered ReHo in the hypothalamus, though hypothalamus’ pathological alterations have been widely reported in depression and cognitive impairment [
37‐
39]. Hence, there may be differences between the rat model and patients with depression in the Reho signal of hypothalamus. Thalamus has been well positioned for an involvement in major depressive disorder pathophysiology, earning its name as the limbic thalamus [
40]. Previous study has showed that cognitive decline may be related to the volume of thalamic atrophy [
41]. In the present study, we found increased Reho within the thalamus in the S group, and notably, a significant negative correlation between the number of rearings in the OFT and the ReHo within the thalamus. Since OFT rearings negatively correlated with the emotionality and anxiety level in rats [
42], our study demonstrated that increased Reho within the thalamus could be served as a potential neuroimaging marker for the depression
. It has been found that the dysfunction of olfactory cortex was closely related with the cognitive impairment [
43]. This study also found a significant positive correlation between the value of B-A and the ReHo values in the olfactory cortex, further confirmed the important role of olfactory cortex in the cognitive function.
In addition to a direct involvement of limbic system, our results demonstrated stress-induced ReHo alterations in other cerebral regions, including the cerebellum, pons, motor cortex, visual cortex, and midbrain. Previous studies have demonstrated ReHo alterations in the pons and cerebellum in depressed patients [
15,
44‐
46], which is consistent with our study. Together, these data suggest that the pons and cerebellum are associated with depression. These abnormalities could serve as markers for the diagnosis of depression and are worth exploring further for their role in the etiology of depression. Besides, since a significant positive correlation was found between the B-A value and the ReHo within the pons, the decreased ReHo in pons could also be a marker of cognitive impairment. The function of the motor cortex has been shown altered in depression [
47], and a decreased ReHo within motor cortex was found in the generalized anxiety disorder patients [
48]. Hence, the result of decreased ReHo within motor cortex in the present study may be a neuroimaging reflection of anxiety. Although several studies have demonstrated abnormal cerebral connectivity involving the visual cortex and midbrain in depression [
49,
50], rare clinical studies reported altered ReHo in the two regions. Since the pathological alterations of the visual cortex and midbrain exist in depression [
51‐
53], there may be also differences between the rat model and patients with depression in the visual cortex and midbrain Reho signal.
Telmisartan has strong anti-inflammatory effects on the brain [
23,
54] and neuroprotective effects in cultured primary neurons [
55], suggesting that telmisartan may be a novel therapeutic approach for the treatment of depression. Some studies suggest that telmisartan can ameliorate memory deficits through beneficially effects on the hippocampus [
56,
57], little is known about which other brain regions are affected by telmisartan. Using ALFF and ReHo, our study demonstrated that stress-induced alterations in multiple brain regions were partly reversed or attenuated by telmisartan. In addition to decreased ReHo measures in the motor cortex and pons due to stress, the motor cortex in the T-1 mg/kg group displayed an increased ReHo compared to the S and C groups, suggesting that telmisartan reversed the motor cortex changes caused by stress. Increased ReHo in the midbrain, thalamus, hippocampus, hypothalamus, visual cortex, and olfactory cortex caused by stress was identified. However, the T-1 mg/kg group exhibited a decreased ReHo in these regions compared to the S group, and increased or unchanged ReHo in these regions compared to the C group. Hence, telmisartan also attenuated or eliminated these stress-induced brain region changes. Besides, since a significant negative correlation was found between the number of rearings in the OFT and the ReHo within the thalamus, telmisartan may attenuate the anxiety symptoms by decreasing the hypercoordination of neural activity within the thalamus. Thalamus could be an important brain region to investigate further in the future study. Other brain regions, including the insular cortex, the sensory cortex, the orbital cortex, and the amygdaloid body, also showed significant differences between the T-1 mg/kg and S groups. However, because there were no significant differences between the S and C groups, it is difficult to determine whether telmisartan had positive or negative effect on these brain regions. Together, our study demonstrated that telmisartan may be a potential antidepressant by beneficially affected a series of brain regions. Future research is required to determine the extent of telmisartan’s effects on the brain in depression.
In conclusion, our study demonstrated widespread alterations in brain regions in a rat model of depression using the ReHo method. These regions consist of some components of the limbic system that contribute to the formation of depression, but also some other regions, such as the motor cortex, visual cortex, midbrain, cerebellum and pons, which are rarely intensively studied for their role in depression. Combined with previous clinical studies, this study revealed that the Reho alterations in several brain rigions could be potential markers for depression and cognitive impairment. Hence, this study suggests future areas for the pathological research of depression. This study also demonstrated that telmisartan can be a complementary medicine for patients with depression, and affects several brain regions. To our best knowledge, this is the first study of the telmisartan’s antidepressant effect on the whole brain in a rat model of depression.
There were several limitations in our study. Firstly, the rats we used are outbred. Since genetic differences may contribute to the behavioral effects of rodents in models of depression [
58], it would be more ideal to use inbred strains in the future. Secondly, we were unable to have a pre- and post-stress brain comparison due to laboratory regulations limiting the physical movement of the animals after r-fMRI. Thirdly, we only observed telmisartan’s effect on the stress model due to our strict animal ethic regulations of limiting the animal number. It will be more rigorous to conduct additional groups to explore whether telmisartan could alter behavior, cognitive function or brain activity in the absence of stress for further study.