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Prefrontal cortex, dorsomedial striatum, and dentate gyrus are necessary in the object-based attention test in mice
Molecular Brain volume 13, Article number: 171 (2020)
Disturbances of attention are a common behavioral feature associated with neuropsychiatric disorders with largely unknown underlying causes. We previously developed an object-based attention test (OBAT) as a simple and practical method for evaluating attention in mice. Since its establishment, the test has become a popular method for assessing attention and related underlying mechanisms in various mouse models. However, the underlying neuronal network involved in this test has yet to be studied. The purpose of this study was to identify the principal brain regions activated in the OBAT. Accordingly, C57BL/6J mice were subjected to the OBAT and thereafter prepared for immunohistochemical quantification of c-Fos, an immediate early gene that is frequently used as a marker of neuronal activity, in 13 different brain regions. The number of c-Fos-positive cells was significantly higher in the prefrontal cortex (PFC), dorsomedial striatum (DMS), and dentate gyrus (DG) in the test group as compared to the control group. The neuronal activation of these brain regions during the OBAT indicates that these brain regions are necessary for the regulation of attention in this test. This was supported by excitotoxic lesioning of these brain regions, leading to impaired attention without causing locomotor dysfunction. This study is one of the first attempts to analyze the brain regions that regulate attention in the OBAT. These findings provide an initial insight into the role of these brain regions and ideas for studying the underlying neural and molecular mechanisms.
Attention plays a critical role in cognition. Impaired attention is often seen in patients with various neuropsychiatric disorders, such as attention-deficit hyperactivity disorder (ADHD), schizophrenia, and major depressive disorder [1,2,3]. We have previously developed an object-based attention test (OBAT) as a simple and practical method suitable for the evaluation of attention in mice . This behavioral test relies on mice’s inherent behavior to explore novelty in the absence of any instrumental training or external reinforcers. The test comprises two phases: training (familiarization) and testing. In the training session, mice are presented with five different shaped but similarly sized objects for familiarization; a novel and familiar object are then presented during testing (Fig. 1a). The principle here is to use the natural curiosity of mice; when a new object is presented, healthy mice recognize the familiar object and spend more time exploring the novel object during testing. Mice with impaired attention spend approximately equal time with the familiar and novel objects. This is similar to paired comparisons used in object-based visual attention tests in human subjects .
Since its establishment, the test has become a popular method to assess attention and related underlying mechanisms in different mouse models [6,7,8]. Among many tasks that have been developed to assess attentional functions in rodents, OBAT is easy to perform and does not require expensive equipment, and therefore may be accessible to investigators on a tight budget. In currently available tasks for assessing attention in mice, the presence of food/liquid reinforcers associated with the choice stimuli might result in an ambiguous interpretation of animal responses and potential bias in choice decisions, making the interpretation of results uncertain . For example, prenatal nicotine exposure in mice is known to alter reward circuits . One of the marked advantages of OBAT over other attention-related tests is the significantly shortened experimental period (e.g., five-choice serial reaction time task, 3–5 months; OBAT, 1 day) [4, 10]. This further emphasizes OBAT as ideal for the evaluation of attention in younger mice, which is a fundamental factor in research related to some disorders, such as ADHD . These characteristics support the use of OBAT as a test for evaluating attention in preclinical studies. However, the underlying neuronal network involved in this test has yet to be studied.
The first aim of the study was to identify the principal brain regions activated by OBAT. C57BL/6J mice were subjected to the OBAT and sacrificed for immunostaining quantification of c-Fos, an immediate early gene that is frequently used as a marker of neuronal activity, in 13 different brain regions (Additional file 1: Table 1). The number of c-Fos-positive cells was significantly higher in the anterior cingulate cortex (ACC), prelimbic (PrL) and infralimbic (IL) cortices of the prefrontal cortex (PFC; Fig. 1b), dorsomedial striatum (DMS; Fig. 1d), and dentate gyrus (DG; Fig. 1f) in the test group compared to those in the control group (no objects in the test session). To further evaluate the importance of these brain regions, we bilaterally lesioned these regions using excitotoxic ibotenic acid in different batches of mice that underwent the OBAT. Ibotenic acid produces excessive Ca2+ through activation of glutamate receptors resulting neuronal cell death, further leads to behavioral changes . There were approximately 50% decreases of neuronal cells in the targeted brain regions (Additional file 2: Figure 1). Mice were given 1 week to fully recover from the surgery. Given the role of the PFC, DMS, and DG in controlling motor function, open field and rota-rod tests were conducted to provide an additional control measure of locomotor function in the lesioned mice (Additional file 2: Figure 1a and b). We confirmed that the impaired attention in lesioned mice was not an artifact of locomotor dysfunction, with no difference between control and lesioned mice in the total distance traveled in the open field or motor skill learning in the rota-rod tests (Additional file 2: Figure 1c, d, f, g, i, j). Mice were subjected to the OBAT on the following day (Fig. 1a). In the training session, control and lesioned mice spent a similar amount of time exploring the objects. In the test session, lesioned mice showed impaired attention, as evidenced by the significantly decreased time spent exploring the novel object (Fig. 1c, e, and g). Statistical analyses were given in the Additional file 1: Table 2.
Taken together, the findings of this study suggest that the PFC, DMS, and DG (but may not be limited to) are necessary for the regulation of attention in the OBAT in mice. These results are consistent with previous studies that the PFC, DMS, and DG are involved in other attention-related tests [12,13,14]. We have successfully identified brain regions activated during the OBAT using c-Fos mapping and confirmed that these areas are involved in the regulation of attention in a lesion study. It should be kept in mind that sensory ability and motivation processes could also contribute the behavioral performance in this test when interpreting the obtained results. However, we cannot distinguish whether the c-Fos was triggered during training or testing because the interval between the sessions was only 10 s (e.g., information processing). Therefore, it is important to develop improved tools to study the specific cell types in specific neuronal projections during the test (including subregional differences in the PFC) by using more temporally precise manipulations, such as optogenetic manipulations, as well as in vivo recording .
Notwithstanding these limitations, this study is one of the first attempts to analyze brain regions activated in the OBAT. These findings provide an initial insight into the roles of these brain regions and suggest how to study the brain circuit interactions and related molecules that contribute to attentional function in normal and disrupted conditions, consequently, suggesting potential treatments for neuropsychiatric disorders.
Availability of data and materials
All data used in this study are available from the corresponding author upon reasonable request.
Anterior cingulate cortex
Attention-deficit hyperactivity disorder
- NAc Core:
Nucleus accumbens core
- NAc Shell:
Nucleus accumbens shell
Object-based attention test
Sommerfeldt SL, Cullen KR, Han G, Fryza BJ, Houri AK, Klimes-Dougan B. Executive attention impairment in adolescents with major depressive disorder. J Clin Child Adolesc Psychol. 2016;45(1):69–83.
Faraone SV, Asherson P, Banaschewski T, Biederman J, Buitelaar JK, Ramos-Quiroga JA, et al. Attention-deficit/hyperactivity disorder. Nat Rev Dis Primers. 2015;1:15020.
Kindler J, Lim CK, Weickert CS, Boerrigter D, Galletly C, Liu D, et al. Dysregulation of kynurenine metabolism is related to proinflammatory cytokines, attention, and prefrontal cortex volume in schizophrenia. Mol Psychiatry. 2019. https://doi.org/10.1038/s41380-019-0401-9.
Alkam T, Hiramatsu M, Mamiya T, Aoyama Y, Nitta A, Yamada K, et al. Evaluation of object-based attention in mice. Behav Brain Res. 2011;220(1):185–93.
Behrmann M, Zemel RS, Mozer MC. Object-based attention and occlusion: evidence from normal participants and a computational model. J Exp Psychol Hum Percept Perform. 1998;24(4):1011–36.
Zhu J, Fan F, McCarthy DM, Zhang L, Cannon EN, Spencer TJ, et al. A prenatal nicotine exposure mouse model of methylphenidate responsive ADHD-associated cognitive phenotypes. Int J Dev Neurosci. 2017;58:26–34.
Wulaer B, Kunisawa K, Hada K, Suento WJ, Kubota H, Iida T, et al. Shati/Nat8l deficiency disrupts adult neurogenesis and causes attentional impairment through dopaminergic neuronal dysfunction in the dentate gyrus. J Neurochem. 2020. https://doi.org/10.1111/jnc.15022.
Huang Z, Hoffman CA, Chelette BM, Thiebaud N, Fadool DA. Elevated anxiety and impaired attention in super-smeller, Kv1.3 knockout mice. Front Behav Neurosci. 2018;12:49.
Scheggia D, Bebensee A, Weinberger DR, Papaleo F. The ultimate intra-/extra-dimensional attentional set-shifting task for mice. Biol Psychiatry. 2014;75(8):660–70.
Patel S, Stolerman IP, Asherson P, Sluyter F. Attentional performance of C57BL/6 and DBA/2 mice in the 5-choice serial reaction time task. Behav Brain Res. 2006;170(2):197–203.
Dunnett SB, Everitt BJ, Robbins TW. The basal forebrain-cortical cholinergic system: interpreting the functional consequences of excitotoxic lesions. Trends Neurosci. 1991;14(11):494–501.
Aoki S, Liu AW, Zucca A, Zucca S, Wickens JR. Role of striatal cholinergic interneurons in set-shifting in the rat. J Neurosci. 2015;35(25):9424–31.
Chudasama Y, Doobay VM, Liu Y. Hippocampal-prefrontal cortical circuit mediates inhibitory response control in the rat. J Neurosci. 2012;32(32):10915–24.
Kim H, Ahrlund-Richter S, Wang X, Deisseroth K, Carlen M. Prefrontal parvalbumin neurons in control of attention. Cell. 2016;164(1–2):208–18.
Yu X, Nagai J, Khakh BS. Improved tools to study astrocytes. Nat Rev Neurosci. 2020;21(3):121–38.
We thank the Education and Research Facility of Animal Models for Human Diseases at Fujita Health University for their assistance.
This work was supported by Grants-in-Aids for Scientific Research from the Japan Society for the Promotion of Science (17H04252, 18K19761, 20K16679, and 20K07931); Private University Research Branding Project from the Ministry of Education, Culture, Sports, Science, and Technology of Japan. All experiments were conducted in compliance with the ARRIVE guidelines. The authors report no biomedical financial interests or potential conflicts of interest.
Ethics approval and consent to participate
Animals were handled in accordance with the guidelines established by the Animal Experimentation Committee of Fujita Health University Graduate School of Medicine (Permit Number: APU19119), the Guiding Principles for the Care and Use of Laboratory Animals approved by the Japanese Pharmacological Society, and the National Institutes of Health Guide for the Care and Use of Laboratory Animals.
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Wulaer, B., Kunisawa, K., Kubota, H. et al. Prefrontal cortex, dorsomedial striatum, and dentate gyrus are necessary in the object-based attention test in mice. Mol Brain 13, 171 (2020). https://doi.org/10.1186/s13041-020-00711-4
- Prefrontal cortex
- Dentate gyrus