- Open Access
Paraventricular hypothalamic vasopressin neurons induce self-grooming in mice
Molecular Brain volume 15, Article number: 47 (2022)
Self-grooming plays an essential role in hygiene maintenance, thermoregulation, and stress response. However, the neural populations involved in self-grooming remain largely unknown. The paraventricular hypothalamic nucleus (PVH) has been implicated in the regulation of self-grooming. Arginine vasopressin-producing neurons are among the major neuronal populations in the PVH (PVHAVP), which play important roles in water homeostasis, blood pressure regulation, feeding, and stress response. Here, we report the critical role of PVHAVP neurons in the induction of self-grooming. Optogenetic activation of PVHAVP neurons immediately induced self-grooming in freely moving mice. Chemogenetic activation of these neurons also increased time spent self-grooming. In contrast, their chemogenetic inhibition significantly reduced naturally occurring self-grooming, suggesting that PVHAVP-induced grooming has physiological relevance. Notably, optogenetic activation of PVHAVP neurons triggered self-grooming over other adaptive behaviors, such as voracious feeding induced by fasting and social interaction with female mice. Thus, our study proposes the novel role of PVHAVP neurons in regulating self-grooming behavior and, consequently, hygiene maintenance and stress response. Furthermore, uncontrolled activation of these neurons may be potentially relevant to diseases characterized by compulsive behaviors and impaired social interaction, such as autism, obsessive–compulsive disorder, and anorexia nervosa.
Animals perform maintenance behaviors for their basic subsistence. Such behaviors include drinking, feeding, washing, grooming, preening, and sleeping. In rodents, self-grooming is a vital maintenance behavior characterized by scratching, licking, or biting the fur, body, whiskers, feet, or genitals . Rodents groom themselves to keep the body clean, maintain body temperature, protect the body from foreign materials, and reduce stress levels . They feed, drink, walk, and explore during the remaining awake time.
In addition to serving the functions of hygiene maintenance and thermoregulation, self-grooming has an essential role in stress response . Self-grooming acts as an adaptive behavior to avoid over-response to stress [1, 4, 5]. On the other hand, over-grooming in rodents is a repetitive, compulsive behavior comparable to obsessive thought or obsessive behavioral change characteristic to some psychiatric disorders, such as obsessive–compulsive disorder, obsessive eating disorder, and autism spectrum disorder [6,7,8,9,10]. Thus, unraveling the brain regions and neuronal populations regulating self-grooming is valuable for understanding the neurobiological basis of hygiene maintenance, stress management, and those psychiatric disorders.
In recent years, the limbic and hypothalamic neural circuits involved in self-grooming behavior have begun to emerge [5, 11,12,13,14]. The paraventricular hypothalamus (PVH) is one of the regions of interest. It is an autonomic control system well-known for its essential roles in metabolism, stress response, and body-fluid homeostasis through its projections to the hypophyseal endocrine system, the autonomic nervous system, and many other brain regions [15,16,17]. Local electrical or pharmacological activation of PVH and surrounding regions have been reported to initiate self-grooming . PVH contains multiple types of neurons that have different physiological functions. Among them, corticotropin-releasing hormone (CRH)-producing neurons (PVHCRH) form the central axis of stress response and have been demonstrated to increase self-grooming in mice upon their optogenetic activation . Consistently, central administration of CRH or adrenocorticotropic hormone (ACTH) elicits self-grooming [19, 20].
AVP-producing neurons are another major neuronal population in the PVH. PVHAVP neurons play a role in water homeostasis, blood pressure regulation, food intake regulation, social interactions, and stress response [21,22,23,24,25,26,27]. In addition, intracerebroventricular administration (ICV) of AVP has been demonstrated to increase grooming [27,28,29,30]. However, the involvement of PVHAVP neurons in the regulation of grooming behavior remains unknown. In this study, we used optogenetics and chemogenetics to address whether these neurons affect self-grooming.
Optogenetic activation of PVHAVP neurons induces self-grooming in freely moving mice
To test whether PVHAVP neurons play a role in self-grooming, we took an optogenetic approach to activate these neurons. We used the stable step-function opsin (SSFO), a variant of channelrhodopsin 2 (ChR2), that remains active for 20–30 min once activated by blue light, mimicking the depolarized state upon enhanced excitatory inputs [31, 32]. To express SSFO specifically in PVHAVP neurons, we unilaterally injected a Cre-On adeno-associated virus vector AAV-EF1α-DIO-SSFO-EYFP in the PVH of mice expressing Cre recombinase specifically in AVP neurons (Avp-Cre mice)  (Fig. 1). We first verified whether SSFO stimulation increases the firing rate of PVHAVP neurons. Slice electrophysiology revealed that activation of SSFO in PVHAVP neurons increased their firing rate (baseline: 4.5 ± 0.6 Hz vs. optogenetic activation: 9.8 ± 0.4 Hz) (Additional file 1: Fig. S1). We also examined in vivo the effects of SSFO stimulation on the activity of PVHAVP neurons. A brief blue-light illumination to PVHAVP neurons via an optic fiber significantly increased c-Fos expression in SSFO-EYFP-expressing PVHAVP neurons compared to control EGFP-expressing PVHAVP neurons (EGFP: 7.8 ± 2.3% vs. SSFO: 77.6 ± 2.9%) (Fig. 2A–D). Thus, PVHAVP neurons can be activated optogenetically in vivo.
Then, we observed mouse behavior after an optogenetic activation of PVHAVP neurons by videorecording in the light period. Upon optogenetic stimulation, freely moving mice immediately exhibited self-grooming (latency: 3.7 ± 0.4 s) (Additional file 2: Video S2). Furthermore, they drastically increased grooming behavior and spent most time grooming during 10 min of observation after stimulation (EGFP: 3.5 ± 1.5% vs. SSFO: 91.1 ± 4.9%) (Fig. 2E–H, Additional file 2: Video S2 and Additional file 3: Video S3). Thus, our result suggested that activation of PVHAVP neurons induces self-grooming in mice.
Self-grooming is not a unitary behavior and contains multiple phases in which animals groom different body parts [1, 5, 34]. Furthermore, previous studies suggested that the patterns of self-grooming are variable and differentially associated with physical and emotional stress . Thus, we compared the pattern of self-grooming induced by the optogenetic activation of PVHAVP neurons with that of spontaneous ones. To do so, we dissected self-grooming behavior into four phases. Namely, (1) paw licking, (2) face/head grooming, (3) body grooming, and (4) leg/tail/genital grooming. During PVHAVP neuron-induced self-grooming, mice spent paw licking for significantly longer at the expense of body/leg/tail/genital grooming than spontaneous self-grooming (Additional file 1: Fig. S2). Such a pattern of PVHAVP neuron-induced self-grooming may resemble those of grooming caused by emotional stress in rats .
Previous studies have reported that some PVHCRH neurons co-express AVP in rats, primarily upon adrenalectomy . Therefore, we confirmed that PVHAVP neurons stimulated optogenetically constituted a population distinct from PVHCRH neurons in our experimental conditions. To do this, we injected a reporter AAV-CAG-FLEX-EGFP in the PVH of Avp-Cre mice. We immunostained brain sections prepared from these mice pretreated with colchicine, which was required to delineate cell bodies with an anti-CRH antibody. Only 3.8 ± 1.2% of EGFP-positive cells were also CRH-positive, whereas AVP-positive cells accounted for 90.6 ± 2.0% of EGFP-positive cells in the PVH (Additional file 1: Fig. S3). This result suggested that optogenetic induction of self-grooming we observed was caused by activation of PVHAVP neurons but not by a part of PVHCRH neurons.
Chemogenetic activation of PVHAVP neurons promotes self-grooming in freely moving mice
Next, we verified the finding of our optogenetic study by the chemogenetic approach. For chemogenetic activation, we expressed hM3Dq, an excitatory Designer Receptors Exclusively Activated by Designer Drugs (DREADD) , in PVHAVP neurons by unilaterally injecting AAV-EF1α-DIO-hM3Dq-mCherry in the PVH of Avp-Cre mice (Fig. 3A and B). The excitatory effect of hM3Dq stimulation on these neurons was verified by slice electrophysiology, showing an increase of firing rate from 5.5 ± 0.9 Hz to 14 ± 1.8 Hz upon CNO application (Additional file 1: Fig. S4A and B). Chemogenetic activation of PVHAVP neurons in vivo by CNO administration significantly increased time spent self-grooming compared to saline administration during 1 h of observation after administration from zeitgeber time (ZT) 3 to ZT4 (Saline: 19.9 ± 4.6% vs. CNO: 76.2 ± 4.8%) (Fig. 3C–F). Thus, our chemogenetic study further confirmed the ability of PVHAVP neurons to promote grooming.
Chemogenetic inhibition of PVHAVP neurons reduces self-grooming in freely moving mice
We next examined whether inhibition of PVHAVP neurons reduces naturally occurring self-grooming in the homecage. To do this, we expressed an inhibitory DREADD, hM4Di , in PVHAVP neurons by bilaterally injecting AAV-EF1α-DIO-hM4Di-mCherry in the PVH of Avp-Cre mice (Fig. 4A and B). The inhibitory effect of hM4Di on these neurons was verified by slice electrophysiology, showing a decrease of firing rate from 7.6 ± 2.3 to 1.8 ± 1.3 Hz upon CNO application (Additional file 1: Fig. S4C and D). Chemogenetic suppression of PVHAVP neurons by CNO administration significantly reduced self-grooming during 1 h of observation after administration from ZT11 to ZT12, when mice generally show an anticipatory increase of wakefulness before the onset of the dark period (Saline: 25.8 ± 2.2% vs. CNO: 4.9 ± 1.8%) (Fig. 4C–F). This result suggested that PVHAVP neurons are involved in the physiological regulation of self-grooming.
Optogenetic activation of PVHAVP neurons causes self-grooming over voracious feeding induced by fasting
We next tested whether the optogenetic activation of PVHAVP neurons could switch other adaptive behaviors triggered by physiological needs into self-grooming. We first examined fasting-induced feeding. Mice expressing SSFO-EYFP in PVHAVP neurons were fasted for 24 h and then refed. Fasted mice spent most time feeding when refed (Fig. 5A, Additional file 4: Video S4). However, optogenetic activation of PVHAVP neurons efficiently suppressed feeding and instead induced self-grooming (latency: 4.7 ± 1.2 s) (Fig. 5A–G, Additional file 5: Video S5). This result suggested that activation of PVHAVP neurons prioritized self-grooming over hunger-induced feeding.
Optogenetic activation of PVHAVP neurons causes self-grooming over social interaction between male and female mice
We also tested whether PVHAVP neuron-induced self-grooming is dominant over social interaction between male and female mice. When exposed to a female mouse, male mice expressing SSFO-EYFP in PVHAVP neurons chased and tried to interact and groom female mice (Fig. 6A, Additional file 6: Video S6). However, optogenetic activation of PVHAVP neurons significantly prevented male mice from interacting with female mice and instead induced self-grooming (latency: 3.7 ± 0.5 s) (Fig. 6A–G, Additional file 7: Video S7). Thus, this result suggested that activation of PVHAVP neurons overrode the need for social interaction and social-grooming to induce self-grooming.
In this study, we found that activation of PVHAVP neurons immediately induces self-grooming. In addition, inhibition of these neurons reduced naturally occurring self-grooming. Intriguingly, stimulation of PVHAVP neurons forced mice to self-groom instead of engaging in the appropriate adaptive behaviors, such as feeding when hungry or social interaction with female mice.
Under normal physiological conditions, mice spent a significant portion of their waking hours self-grooming. Mice use their tongues to lick their bodies and hairs to keep them clean, scratch their bodies with their paws to relieve itchiness, and nibble on their hairs and bodies to remove dust, foreign materials and parasite . In this way, self-grooming maintains hygiene and reduces the risk of contracting infectious diseases. Furthermore, self-grooming behavior occurs frequently when mice are subjected to emotional stresses such as restraint stress, water spray, exposure to light, and forced swimming [5, 11, 34, 37]. For mice, self-grooming seems a means of relieving emotional stress [1, 4, 5].
Multiple neural circuits in the limbic system and hypothalamus have been reported to regulate self-grooming [5, 11,12,13,14]. Mangieri et al. demonstrated that optogenetic activation of Sim1-positive PVH neurons induced self-grooming and competed with hunger-induced feeding . They further reported that glutamatergic PVH → ventral lateral septum (LSv) projections of those PVH neurons lacking CRH, oxytocin, and AVP constitute the major component of this behavioral circuit [11, 12]. On the other hand, PVHCRH neurons have also been demonstrated to promote grooming behavior significantly in mice when optogenetically stimulated . Because some PVHCRH neurons were reported to express AVP, the formal possibility remains that PVHAVP neurons we stimulated in the current study overlapped with PVHCRH neurons, and we observed the same phenomena as those by Füzesi et al. . However, we consider this possibility very unlikely. First, AVP expression in PVHCRH neurons is negligible at the basal conditions and increases after adrenalectomy . In addition, CRH neuron-specific Cre driver mice used in Füzesi et al. demonstrated marginal colocalization (~ 5%) of Cre and AVP expression in the PVH . Furthermore, we confirmed little overlap (~ 4%) between CRH immunoreactivity and PVHAVP neurons we studied.
During PVHCRH stimulation, mice spent ~ 30% of their time grooming , much less than the activation of PVHAVP neurons shown in this study. PVHCRH neurons are likely to orchestrate complex behaviors after stress, one of which is self-grooming . On the other hand, the rapid and stereotypical induction of grooming suggested that PVHAVP neurons may be more specialized in triggering self-grooming behavior. PVHAVP neurons enhance the stress-induced ACTH secretion from the anterior pituitary . Therefore, these neurons may be well-positioned to regulate multiple aspects of the stress response. Nevertheless, the rapid induction of self-grooming by PVHAVP activation indicates that this induction was caused by a neural mechanism and was not secondary to the endocrine mechanism. The target brain regions of PVHAVP neurons and the interaction between PVHCRH and PVHAVP neurons in the regulation of self-grooming should be elucidated in future studies.
The increase of paw licking compared to spontaneous self-grooming may implicate the similarity of PVHAVP neuron-induced self-grooming to grooming induced by emotional stress. The patterns of self-grooming are variable and may reflect differences in the context [1, 5, 34]. Mu et al. showed in rats that the patterns are different between self-grooming associated more with physical stress and that with emotional stress, such as body restraint and bright light exposure . Intriguingly, self-grooming induced by restraint and light exposure contained paw licking more than physical stress-induced and spontaneous self-grooming. They also demonstrated that the hippocampal ventral subiculum (VS) → LSv → lateral hypothalamus tuberal nucleus is the circuitry critical for emotional stress-induced grooming. Reportedly, PVHAVP neurons receive direct inputs from the LSv . Moreover, bed nucleus of stria terminalis (BNST) is another stress-responsive region that projects PVHAVP neurons  and has been implicated in the regulation of self-grooming . Therefore, these projections to PVHAVP neurons from the LSv and BNST may be involved in stress-induced grooming.
The repetitive self-grooming behavior at the expense of social interaction observed in PVHAVP-activated mice was similar to the symptoms of autism spectrum disorder, namely limited social interaction, reduced communication, and repetitive behaviors [43, 44]. Repetitive behaviors are also shared by people with obsessive–compulsive disorder (OCD), who have uncontrollable obsessive thoughts and compulsive behaviors [45, 46]. Repetitive self-grooming and increased paw licking induced by the activation of PVHAVP neurons appears to be comparable to frequent hand-washing in OCD patients. Our findings may also be relevant to the obsessive compulsion shown by people with eating disorders [7, 47, 48]. For instance, anorexia nervosa patients skip food even though they are hungry and show compulsive behaviors [47, 49]. Similarly, PVHAVP-induced self-grooming overrode fasting-induced feeding. A previous report that activation of PVHAVP neurons reduces food intake in fasted mice may be better interpreted in the same context .
In conclusion, PVHAVP neurons play an essential role in the regulation of self-grooming. Their activation triggers grooming at the expense of other adaptive behaviors such as feeding and social interaction. Thus, our study proposes novel functions of PVHAVP neurons in the maintenance behaviors, stress responses, and the pathophysiology of diseases related to repetitive behaviors. Artificial manipulations of self-grooming levels via PVHAVP neurons and identification of input and output pathways of PVHAVP neurons might promote a better understanding of the physiological meanings of such an intriguing behavior.
Hemizygous Avp-Cre mice bred on the C57BL/6 J background, reported previously , were used in the present study. We used 12 to 32-week-old male mice, weighing 26–40 g at the time of surgery. Mice were housed under a 12-h light/12-h dark cycle in a temperature- and humidity-controlled room and provided free access to food and water. All experimental procedures were approved by the appropriate institutional animal care and use committees of Kanazawa University. We made every effort to minimize the number of animals used for the experiments and reduce any pain or discomfort experienced by the mice.
Generation of recombinant viral vectors
The plasmid pAAV-EF1a-DIO-SSFO-EYFP was obtained from Dr. Karl Deisseroth as a gift. The plasmids pAAV-EF1a-DIO-hM3Dq-mCherry, and pAAV-EF1a-DIO-hM4Di-mCherry were obtained from Dr. Bryan Roth as gifts. The plasmid pAAV-CAG-FLEX-EGFP was constructed from plasmid pGP-AAV-CAG-FLEX-jGCaMP7s-WPRE (Addgene plasmid #104495, a gift from Dr. Douglas Kim & GENIE Project) by replacing jGCaMP7s with EGFP.
Using a triple transfection helper-free method, recombinant AAV vectors (AAV2-rh10) were produced and purified as described previously . The titers of recombinant AAV vectors were determined by quantitative real-time PCR (genome copies per mL): AAV-EF1a-DIO-SSFO-EYFP, 1.8 × 1012; AAV-CAG-FLEX-EGFP, 1.0 × 1013; AAV-EF1a-DIO-hM3Dq-mCherry, 1.2 × 1013; AAV-EF1a-DIO-hM4Di-mCherry, 1.9 × 1012.
Stereotaxic injection of AAV vectors was performed as described previously . Mice were anesthetized first with the mixture of medetomidine hydrochloride (0.3 mg/kg, Zenoaq), midazolam (4 mg/kg, Astellas), and butorphanol tartrate (5 mg/kg, Meiji Seika Pharma). When mice lost consciousness, they were placed in the stereotaxic apparatus, and holes were made in the head skull according to requirements. Using a Hamilton Neuros Syringe, 1 μL of AAV vectors was injected unilaterally or bilaterally in the PVH (0.9 mm posterior, ± 0.3 mm lateral, 4.8 mm ventral, relative to the bregma) at a rate of 0.1 μL/min. After 10 min of rest, the needles were removed from the injection site. For optogenetic experiments, an optic fiber (200 μm core, N.A. 0.39, 6 mm, ferrule 1.25 mm, FT200EMT-CANNULA; Thorlabs) was implanted above the PVH (0.9 mm posterior, 0.3 mm lateral, 4.5 mm ventral, relative to the bregma), and then secured to the skull and skin with the dental cement. After the surgical procedure, mice were administered with atipamezole hydrochloride (0.3 mg/kg, Zenoaq) to regain consciousness. Mice were housed individually after surgery and allowed to recover for at least two weeks before starting the experiments.
Slice electrophysiology was performed as described previously . We expressed SSFO-EYFP, hM3Dq-mCherry, or hM4Di-mCherry in the PVH of Avp-Cre mice by focally injecting the corresponding AAV vectors. After 2–4 weeks, the mice were decapitated under deep anesthesia with isoflurane. Brains were extracted and cooled in ice-cold cutting solution containing following compounds in mM concentration: 87 NaCl, 75 sucrose, 25 NaHCO3, 1.25 NaH2PO4, 2.5 KCl, 0.5 CaCl2, 7 MgCl2, and 10 D( +)-glucose, bubbled with O2 95% and CO2 5%. Coronal brain slices of 250 μm thickness containing PVH were prepared with a vibratome (NLS-MT, Dosaka EM). The brain slices were incubated at room temperature for at least 1 h in artificial cerebrospinal fluid (ACSF) containing the following compounds in mM concentration: 125 NaCl, 26 NaHCO3, 1.25 NaH2PO4, 2.5 KCl, 2 CaCl2, 1 MgSO4, and 10 D( +)-glucose, bubbled with O2 95% and CO2 5%. Then the slices were transferred to a recording chamber on a fluorescent microscope stage and continuously perfused with ACSF. EYFP, hM3Dq-mCherry, or hM4Di-mCherry-expressing neurons were identified in the PVH for recording. Cell-attached and whole-cell patch-clamp recordings were performed at 31 °C with borosilicate glass electrodes (4–6 MΩ) prepared by a micropipette puller (P-97, Sutter Instrument) and filled with an internal solution containing the following (mM): 125 K-gluconate, 10 HEPES, 0.2 EGTA, 4 NaCl, 2 MgCl2, 4 ATP, 0.4 GTP, and 10 phosphocreatine, pH 7.3, adjusted with KOH. A combination of an amplifier (EPC 10/2, HEKA) and Patch master software (HEKA) was used to control membrane voltage, data acquisition, and triggering of light pulses. To activate SSFO-EYFP, blue (470 nm) light was generated from a solid-state light illuminator (Spectra X light engine, Lumencor). For in vitro hM3Dq-mcherry activation and hM4Di-mcherry inhibition purpose, 10 µM CNO was bath applied during slice electrophysiology.
Intracardial perfusion, preparation of serial brain sections, and double immunostaining were performed as described previously . Mice were anesthetized and then fixed by intracardiac perfusion with 4% paraformaldehyde (PFA) in PBS. Serial coronal brain sections of 30 μm thickness were prepared with a cryostat (CM1860, Leica) and collected in 4 series—one of which was further immunostained. Primary antibodies used were guinea pig anti-AVP antibody (1:5000; T-5048, Peninsula Laboratories), rabbit anti-CRH antibody (1:2000; HAC-HM04-01RBP90, the joint/usage research program of the Institute for Molecular and Cellular Regulation, Gunma University for anti-CRH antibody), rabbit anti-GFP antibody (1:1000; A11122, Thermo Fisher Scientific), rat anti-GFP antibody (1:800; 04404-84, Nacalai Tesque), and rabbit anti-c-Fos antibody (1:5000; ABE457, Merck Millipore). Secondary antibodies used were Alexa Fluor 488-conjugated anti-rabbit IgG antibody (1:2000; A-21206, Thermo Fisher Scientific), Alexa Fluor 488-conjugated anti-rat antibody (1:800; A-21208, Thermo Fisher Scientific), Alexa Fluor 594-conjugated anti-guinea pig IgG antibody (1:2000; 11076, Thermo Fisher Scientific), and Alexa Fluor 594-conjugated anti-rabbit IgG antibody (1:2000; A-21207, Thermo Fisher Scientific). Images were taken by an epifluorescence microscope (BZ-9000, Keyence) or a confocal microscope (Fluoview Fv10i, Olympus).
For optogenetic studies, the viral vector AAV-EF1a-DIO-SSFO-EYFP was focally injected in the PVH of Avp-Cre mice, and optic fiber was placed above the PVH, as described above. After at least two weeks from the surgery, individual mice were transferred to the acrylic cage and habituated for at least three days before starting the optogenetic experiment. For blue-light delivery, the implanted optic fiber was connected to an optical cable at least one day before optogenetic stimulation. Then, mice were subjected to a light pulse (2 s, 473 nm, 1–2 mW/mm2 at the tip of the optic cable; DL-473 laser, Rapp OptoElectronic) and videorecorded their behavior. Optogenetic experiments were conducted between ZT4 and ZT11. To confirm that PVHAVP neurons were activated by blue-light illumination, we examined cFos expression in these neurons. To do this, two 2-s blue-light pulses were delivered with an interval of 20 min, and then the mice were perfused 70 min after the second light pulse.
To analyze the patterns of self-grooming behavior, four different phases of grooming activities were defined, including paw licking, face/head grooming, body grooming, and leg/tail/genital grooming, according to conventional protocol [1, 5, 34]. To obtain data for spontaneous self-grooming, we videorecorded behavior of Avp-Cre mice for 2–3 h between ZT3 and ZT11. The time spent in each phase was expressed as a percentage of the total grooming time, because the grooming time varied from mouse to mouse.
For chemogenetic activation experiment, mCherry-tagged hM3Dq, an excitatory DREADD, was expressed in PVHAVP neurons unilaterally by focally injecting the AAV vector AAV-EF1a-DIO-hM3Dq-mCherry in the PVH of Avp-Cre mice. For chemogenetic inhibition experiment, the AAV vector AAV-EF1a-DIO-hM4Di-mCherry was injected in the PVH bilaterally. Mice were administered with CNO (5 mg/kg body weight; 34233-69-7, Cayman Chemical) or saline intraperitoneally (i.p.) 20 min before starting the videorecording. Mice were videorecorded from ZT3 to ZT4 for the chemogenetic activation study, or ZT11 to ZT12 for the chemogenetic inhibition study. Each mouse received one saline and one CNO administrations in an alternating manner at an interval of 3 d. Mice were habituated to i.p injection for at least three consecutive days before starting the experiment.
Food deprivation test
After habituation in the acrylic cage for at least three days, individual mice with an optic fiber implant and SSFO expression in PVHAVP neurons were food-deprived for approximately 24 h. Then mice were videorecorded for 10 min during refeeding. After at least 7 d with free access to food, mice were given the same food deprivation-refeeding protocol except for a 2-s blue-light illumination to PVHAVP neurons at the onset of refeeding. Experiments were conducted between ZT4 and ZT11.
Male–female interaction test
Initially, individual male mice with an optic fiber implant and SSFO expression in PVHAVP neurons were habituated in the acrylic cage for at least 3 days. Then, a female wildtype mouse was introduced in the cage, and the behavior of mice were videorecorded for 10 min. After being housed singly for at least 1–2 days, mice were given the same male–female interaction protocol except for a 2-s blue-light illumination to PVHAVP neurons at the onset of the introduction of female mice. Experiments were conducted between ZT4 and ZT11.
As described in the respective figure legend, statistical analyses included Welch's t-test and paired t-test, performed using Prism 7.0 software (GraphPad). All data are presented as mean ± SEM. p < 0.05 was considered statistically significant.
Availability of data and materials
All relevant data are within the paper and supporting information files.
Paraventricular hypothalamic nucleus
Stable step-function opsin
Enhanced yellow fluorescent protein
Enhanced green fluorescent protein
Designer receptors exclusively activated by designer drugs
Human M3 muscarinic cholinergic Gq-coupled receptor
Human M4 muscarinic cholinergic Gi-coupled receptor
Kalueff AV, Stewart AM, Song C, Berridge KC, Graybiel AM, Fentress JC. Neurobiology of rodent self-grooming and its value for translational neuroscience. Nat Rev Neurosci. 2016;17:45–59.
Bolles RC. Grooming behavior in the rat. J Comp Physiol Psychol. 1960;53:306.
Liu H, Huang X, Xu J, Mao H, Li Y, Ren K, et al. Dissection of the relationship between anxiety and stereotyped self-grooming using the Shank3B mutant autistic model, acute stress model and chronic pain model. Neurobiol Stress. 2021;15: 100417.
Langen M, Kas MJH, Staal WG, van Engeland H, Durston S. The neurobiology of repetitive behavior: of mice…. Neurosci Biobehav Rev. 2011;35:345–55.
Mu M-D, Geng H-Y, Rong K-L, Peng R-C, Wang S-T, Geng L-T, et al. A limbic circuitry involved in emotional stress-induced grooming. Nat Commun. 2020;11:1–16.
Zhou Y, Kaiser T, Monteiro P, Zhang X, Van der Goes MS, Wang D, et al. Mice with Shank3 mutations associated with ASD and schizophrenia display both shared and distinct defects. Neuron. 2016;89:147–62.
Levinson CA, Brosof LC, Ram SS, Pruitt A, Russell S, Lenze EJ. Obsessions are strongly related to eating disorder symptoms in anorexia nervosa and atypical anorexia nervosa. Eat Behav. 2019;34: 101298.
Godier LR, Park RJ. Compulsivity in anorexia nervosa: a transdiagnostic concept. Front Psychol. 2014;5:778.
Cath DC, Ran N, Smit JH, Van Balkom AJLM, Comijs HC. Symptom overlap between autism spectrum disorder, generalized social anxiety disorder and obsessive-compulsive disorder in adults: a preliminary case-controlled study. Psychopathology. 2008;41:101–10.
Barnard-Brak L, Watkins L, Richman DM. Examining the correlation between symptoms of obsessive compulsive disorder and autism spectrum disorder in a community-based sample of adults. Psychiatry Res. 2021;299: 113826.
Mangieri LR, Lu Y, Xu Y, Cassidy RM, Xu Y, Arenkiel BR, et al. A neural basis for antagonistic control of feeding and compulsive behaviors. Nat Commun. 2018;9:1–15.
Xu Y, Lu Y, Cassidy RM, Mangieri LR, Zhu C, Huang X, et al. Identification of a neurocircuit underlying regulation of feeding by stress-related emotional responses. Nat Commun. 2019;10:1–16.
Füzesi T, Daviu N, Cusulin JIW, Bonin RP, Bains JS. Hypothalamic CRH neurons orchestrate complex behaviours after stress. Nat Commun. 2016;7:1–14.
Hong W, Kim D-W, Anderson DJ. Antagonistic control of social versus repetitive self-grooming behaviors by separable amygdala neuronal subsets. Cell. 2014;158:1348–61.
Ferguson AV, Latchford KJ, Samson WK. The paraventricular nucleus of the hypothalamus—a potential target for integrative treatment of autonomic dysfunction. Expert Opin Ther Targets. 2008;12:717–27.
Sutton AK, Myers MG Jr, Olson DP. The role of PVH circuits in leptin action and energy balance. Annu Rev Physiol. 2016;78:207–21.
Swanson LW, Sawchenko PE. Paraventricular nucleus: a site for the integration of neuroendocrine and autonomic mechanisms. Neuroendocrinology. 1980;31:410–7.
Roeling TAP, Veening JG, Peters JPW, Vermelis MEJ, Nieuwenhuys R. Efferent connections of the hypothalamic “grooming area” in the rat. Neuroscience. 1993;56:199–225.
Veldhuis HD, De Wied D. Differential behavioral actions of corticotropin-releasing factor (CRF). Pharmacol Biochem Behav. 1984;21:707–13.
Van Erp AMM, Kruk MR, Willekens-Bramer DC, Bressers WMA, Roeling TAP, Veening JG, et al. Grooming induced by intrahypothalamic injection of ACTH in the rat: comparison with grooming induced by intrahypothalamic electrical stimulation and icv injection of ACTH. Brain Res. 1991;538:203–10.
Zimmerman CA, Leib DE, Knight ZA. Neural circuits underlying thirst and fluid homeostasis. Nat Rev Neurosci. 2017;18:459–69.
Bankir L, Bichet DG, Morgenthaler NG. Vasopressin: physiology, assessment and osmosensation. J Intern Med. 2017;282:284–97.
Lozić M, Šarenac O, Murphy D, Japundžić-Žigon N. Vasopressin, central autonomic control and blood pressure regulation. Curr Hypertens Rep. 2018;20:1–7.
Pei H, Sutton AK, Burnett KH, Fuller PM, Olson DP. AVP neurons in the paraventricular nucleus of the hypothalamus regulate feeding. Mol Metab. 2014;3:209–15.
Beurel E, Nemeroff CB. Interaction of stress, corticotropin-releasing factor, arginine vasopressin and behaviour. Behav Neurobiol Stress Disord. 2014. https://doi.org/10.1007/7854_2014_306.
Bendesky A, Kwon Y-M, Lassance J-M, Lewarch CL, Yao S, Peterson BK, et al. The genetic basis of parental care evolution in monogamous mice. Nature. 2017;544:434–9.
Bielsky IF, Hu S-B, Szegda KL, Westphal H, Young LJ. Profound impairment in social recognition and reduction in anxiety-like behavior in vasopressin V1a receptor knockout mice. Neuropsychopharmacology. 2004;29:483–93.
Lumley LA, Robison CL, Chen WK, Mark B, Meyerhoff JL. Vasopressin into the preoptic area increases grooming behavior in mice. Physiol Behav. 2001;73:451–5.
Meisenberg G. Vasopressin-induced grooming and scratching behavior in mice. Ann N Y Acad Sci. 1988;525:257–69.
Delanoy RL, Dunn AJ, Tintner R. Behavioral responses to intracerebroventricularly administered neurohypophyseal peptides in mice. Horm Behav. 1978;11:348–62.
Yizhar O, Fenno LE, Prigge M, Schneider F, Davidson TJ, O’shea DJ, et al. Neocortical excitation/inhibition balance in information processing and social dysfunction. Nature. 2011;477:171–8.
Berndt A, Yizhar O, Gunaydin LA, Hegemann P, Deisseroth K. Bi-stable neural state switches. Nat Neurosci. 2009;12:229–34.
Mieda M, Ono D, Hasegawa E, Okamoto H, Honma K, Honma S, et al. Cellular clocks in AVP neurons of the SCN are critical for interneuronal coupling regulating circadian behavior rhythm. Neuron. 2015;85:1103–16.
Kalueff AV, Tuohimaa P. The grooming analysis algorithm discriminates between different levels of anxiety in rats: potential utility for neurobehavioural stress research. J Neurosci Methods. 2005;143:169–77.
Whitnall MH, Mezey Ė, Gainer H. Co-localization of corticotropin-releasing factor and vasopressin in median eminence neurosecretory vesicles. Nature. 1985;317:248–50.
Armbruster BN, Li X, Pausch MH, Herlitze S, Roth BL. Evolving the lock to fit the key to create a family of G protein-coupled receptors potently activated by an inert ligand. Proc Natl Acad Sci. 2007;104:5163–8.
Chesher GB, Jackson DM. Swim-induced grooming in mice is mediated by a dopaminergic substrate. J Neural Transm. 1981;50:47–55.
Sawchenko PE. Evidence for a local site of action for glucocorticoids in inhibiting CRF and vasopressin expression in the paraventricular nucleus. Brain Res. 1987;403:213–24.
Wamsteeker Cusulin JI, Füzesi T, Watts AG, Bains JS. Characterization of corticotropin-releasing hormone neurons in the paraventricular nucleus of the hypothalamus of Crh-IRES-Cre mutant mice. PLoS ONE. 2013;8: e64943.
Antoni FA. Magnocellular vasopressin and the mechanism of “glucocorticoid escape.” Front Endocrinol. 2019;10:422.
Wei H-H, Yuan X-S, Chen Z-K, Chen P-P, Xiang Z, Qu W-M, et al. Presynaptic inputs to vasopressin neurons in the hypothalamic supraoptic nucleus and paraventricular nucleus in mice. Exp Neurol. 2021;343: 113784.
Wu W-L, Cheng S-J, Lin S-H, Chuang Y-C, Huang EY-K, Chen C-C. The effect of ASIC3 knockout on corticostriatal circuit and mouse self-grooming behavior. Front Cell Neurosci. 2019;13:86.
Osterling JA, Dawson G, Munson JA. Early recognition of 1-year-old infants with autism spectrum disorder versus mental retardation. Dev Psychopathol. 2002;14:239–51.
Osterling J, Dawson G. Early recognition of children with autism: a study of first birthday home videotapes. J Autism Dev Disord. 1994;24:247–57.
Bloch MH, Landeros-Weisenberger A, Rosario MC, Pittenger C, Leckman JF. Meta-analysis of the symptom structure of obsessive-compulsive disorder. Am J Psychiatry. 2008;165:1532–42.
Mataix-Cols D, do Rosario-Campos MC, Leckman JF. A multidimensional model of obsessive-compulsive disorder. Am J Psychiatry. 2005;162:228–38.
Mills IH, Medlicott L. Anorexia nervosa as a compulsive behaviour disease. QJM Int J Med. 1992;83:507–22.
Pollack LO, Forbush KT. Why do eating disorders and obsessive–compulsive disorder co-occur? Eat Behav. 2013;14:211–5.
Godier LR, Park RJ. Does compulsive behavior in anorexia nervosa resemble an addiction? A qualitative investigation. Front Psychol. 2015;6:1608.
Hasegawa E, Yanagisawa M, Sakurai T, Mieda M. Orexin neurons suppress narcolepsy via 2 distinct efferent pathways. J Clin Invest. 2014;124:604–16.
Hasegawa E, Maejima T, Yoshida T, Masseck OA, Herlitze S, Yoshioka M, et al. Serotonin neurons in the dorsal raphe mediate the anticataplectic action of orexin neurons by reducing amygdala activity. Proc Natl Acad Sci. 2017;114:E3526–35.
We thank Penn Vector Core for pAAV2-rh10; K. Deisseroth for pAAV-EF1a-DIO-SSFO-EYFP; B. Roth for pAAV-EF1a-DIO-hM3Dq-mCherry and pAAV-EF1a-DIO-hM4Di-mCherry; D. Kim & GENIE Project for pGP-AAV-CAG-FLEX-jGCaMP7s-WPRE; the joint/usage research program of the Institute for Molecular and Cellular Regulation, Gunma University for anti-CRH antibody (HAC-HM04-01RBP90); H. Okamoto for technical support to generate Avp-Cre mouse. We thank Y. Tsuno for discussion; M. Fukushi, and M. Kawabata for technical assistance.
This study was supported in part by MEXT/JSPS KAKENHI Grant Numbers JP16H05120, JP19H03399, JP20K21498; by the Takeda Science Foundation; by the Naito Foundation; by the Daiichi Sankyo Foundation of Life Science; by the Kao Research Council for the Study of Healthcare Science; and by Kanazawa University CHOZEN project (M.M.); by KAKENHI JP18K06519 (T.M.); by MEXT Japanese Government Scholarship for International Students (M.T.I.).
Ethics approval and consent to participate
All experimental procedures were approved by the appropriate institutional animal care and use committees of Kanazawa University. Consent to participate is not applicable for this study.
Consent for publication
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Stimulation of SSFO in PVHAVP neurons increases their firing frequency in slices. Figure S2. Patterns of spontaneous and optogenetically-induced self-grooming. Figure S3. Targeted PVHAVP neurons constitute a population distinct from PVHCRH neurons. Figure S4. Stimulation of hM3Dq or hM4Di in PVHAVP neurons increases or decreases their firing frequency in slices.
About this article
Cite this article
Islam, M.T., Maejima, T., Matsui, A. et al. Paraventricular hypothalamic vasopressin neurons induce self-grooming in mice. Mol Brain 15, 47 (2022). https://doi.org/10.1186/s13041-022-00932-9
- Paraventricular hypothalamic nucleus
- Repetitive behavior