Antistress effects of Kampo medicine "Yokukansan" via regulation of orexin secretion.

OBJECTIVE: Various stressors induce stress responses through the hypothalamic-pituitary-adrenal and the sympathetic-adrenal-medullary axes, which are regulated, in part, by orexin. For example, secretion of orexin in the hypothalamus is increased in rats exposed to the stress of social isolation for 1 week. In this study, the antistress effects of Kampo medicine Yokukansan (YKS) via the regulation of orexin secretion were investigated using a rat model. METHODS AND
RESULTS: The administration of 300 mg/kg per day of YKS to rats for 1 week significantly decreased the plasma orexin levels compared with non-treated rats, whereas the administration of 1,000 mg/kg of YKS had no effect on orexin levels. Therefore, 300 mg/kg of YKS was an effective dose for controlling orexin secretion. Subsequently, rats were divided into group-housed control (Con), individually housed stress (Stress), and individually housed YKS (300 mg/kg)-treated stress (Stress + YKS) groups. After 1 week, a resident-intruder aggression test was performed, and the plasma levels of orexin and corticosterone were measured. In the Stress group, aggressive behavior and the levels of corticosterone and orexin significantly increased compared with the Con group; however, these effects were inhibited in the Stress + YKS group. Further, an orexin receptor antagonist (TCS 1102; 10 mg/kg) was intraperitoneally administered to rats exposed to isolation stress to determine whether orexin was involved in stress responses. Under these conditions, aggressive behavior and the level of corticosterone significantly decreased compared with the Stress group.
CONCLUSION: These results suggest that orexin is involved in the control of stress response and that YKS exerts an antistress effect via the regulation of orexin secretion.

Introduction

Stress causes anxiety, nervousness, and anger as well as physical and behavioral changes. Further, stress affects the autonomic nervous system, endocrine system, and immune system and is involved in the onset and exacerbation of diverse diseases, including psychological disorders such as depression and anxiety. Stressors induce stress responses through the hypothalamic–pituitary–adrenal (HPA) and the sympathetic–adrenal–medullary (SAM) axes. Moreover, orexin is involved in the regulation of these axes.1–3

Orexins (also called hypocretins) are neuropeptides, and orexins A and B are derived from the same precursor peptide, prepro-orexin.4 Orexinergic neurons are mainly expressed in the lateral and perifornical areas of the posterior hypothalamus, and their axons are widely distributed throughout the central nervous system, except in the cerebellum.4 Orexins A and B bind to the orphan G-protein-coupled receptor, orexin-1 receptor (OX1R), which is highly selective for orexin A, and the orexin-2 receptor (OX2R) is nonselective for orexins A and B.4 Orexins are involved in the modulation of multiple physiological processes such as sleep, arousal, feeding, metabolism,3 nociception,5,6 and in the autonomic regulation of the cardiovascular,7 respiratory,8 and neuroendocrine systems.9

Yokukansan (YKS; Yi-Gan San in Chinese), which was first reported in the Bao-ying jin-jing-lu (written in 1550), is a traditional herbal (Kampo) medicine comprising seven herbs (Table 1).10 The herbs are mixed and extracted with purified water at 95.1°C for 1 h, and the soluble extract is separated from the insoluble waste and then concentrated by removing water under reduced pressure. The constituents of the YKS extract are identified using three-dimensional high-performance liquid chromatographic analysis (Figure 1). YKS is administered to patients with symptoms such as emotional irritability, neurosis, and insomnia as well as to infants who cry at night and experience convulsions.10

Table 1

Component galenicals of YKS

Uncariae cum Uncis ramulus	3.0 g
Cnidii rhizoma	3.0 g
Bupleuri radix	2.0 g
Atractylodis Lanceae rhizoma	4.0 g
Poria	4.0 g
Angelicae radix	3.0 g
Glycyrrhizae radix	1.5 g

Note: Weights show the mixing amounts.

Abbreviation: YKS, Yokukansan.

Figure 1

Constituents of the YKS extract.

Note: Constituents of the YKS extract were identified using 3D HPLC from Tsumara & Co. in-house data. Reused with permission from © 2001 Tsumura & Co., Tokyo, Japan.

Abbreviations: 3D, three-dimensional; HPLC, high-performance liquid chromatography; YKS, Yokukansan.

Studies of animals demonstrate the antidepressant, antiaggressive, and anxiolytic effects of YKS;11–15 however, the mechanisms of the psychopharmacologic effects of YKS are incompletely characterized. Further, there are no published studies, to our knowledge, of the effects of YKS on the orexinergic system.

The current study was designed using a rat model of social isolation stress to determine whether the administration of YKS exerts its antistress effect via the regulation of orexin secretion. This animal model is used to study psychological stress induced by a loss of social interaction. Rats live in the wild in groups, and when housed alone, they show stress responses, such as adrenomegaly; increased secretion of adrenocorticotropin (ACTH), corticosterone, and catecholamine;16 aggressive behavior;11 locomotor hyperactivity;17 increase in food intake;18 and oxidative DNA damage.19 In the current study, to evaluate the antistress effect of YKS, we investigated the aggressive behavior of rats and changes in their food intake, plasma corticosterone levels, and orexin secretion.

Materials and methods

Rats

Male Wistar rats (7-weeks-old, weighing 200–230 g) were purchased from Nippon Bio-Supp. Center (Tokyo, Japan). During the experiment, animals were housed in standard plastic cages (for a group raising in a W 24× L 40× H 20 cm cage and for a single raising in a W 26× L 26× H 18 cm cage) and were kept in our animal facility at 25°C±2°C, 55%±5% humidity, with a light/dark cycle of 12 h. Food (CE-2; Clea Japan, Inc., Tokyo, Japan) and water were provided ad libitum. Experiments were performed according to the guidelines of the Committee of Animal Care and Welfare of Showa University. All experimental procedures were approved by the Committee of Animal Care and Welfare of Showa University (certificate number: 02094).

Drugs

YKS (Lot No 2110054010; Tsumura & Co., Tokyo, Japan) was dissolved in distilled water and orally administered. TCS 1102, a dual orexin receptor antagonist (DORA; 916141-36-1; Tocris Bioscience, Bristol, UK), was dissolved in 50% dimethyl sulfoxide (049-07213; Wako Pure Chemical Industries, Osaka, Japan) and intraperitoneally administered.

Influence of YKS on orexin secretion

To determine the influence of YKS on orexin secretion, 18 rats were randomly divided into groups as follows: 1) group-housed control (Con); 2) YKS 300 mg/kg (YKS300); and 3) YKS 1,000 mg/kg (YKS1000). Rats were housed in groups of three per cage. Doses of YKS, which were chosen according to the results of published studies,11–15,20–26 were administered daily for 7 days to the YKS groups, and water was administered orally to the Con group. On day 8, rats were anesthetized with intraperitoneally administered pentobarbital sodium (50 mg/kg; Somnopentyl; Kyoritsu Seiyaku, Tokyo, Japan), and blood samples were taken from the inferior vena cava. To avoid influences of daily fluctuation, all blood samplings were performed from 1:00 to 3:00 pm. Plasma orexin A level was measured using an enzyme-linked immunosorbent assay (ELISA) kit (EKE-003-30; Phoenix Pharmaceuticals, Burlingame, CA, USA).

Antistress effects of YKS

Rat model of social isolation-induced stress

Effects of YKS on psychological stress were investigated using a social isolation model. A total of 21 rats were randomly divided into groups of seven as follows: 1) Con, 2) individually housed stress (Stress), and 3) YKS (300 mg/kg)-treated stress (Stress + YKS). Rats in the Stress and the Stress + YKS groups were individually housed for 8 days, and those in the Con group were housed in groups of two or three per cage. YKS (300 mg/kg) was orally administered to the Stress + YKS group daily for 7 days, and water was administered orally to the other groups.

Food intake measurement

Orexin is reported to control eating behavior,3 and the 24 h food intake was measured at 1:00 pm on days 2 and 7, according to a previous study.18 For the group-housed rats, the total food intake per cage was divided by the number of animals to calculate the food intake per animal for each cage, because food intake of individual rats was impossible to measure.

Aggressive behavior test

On day 7, aggressive behavior was analyzed according to a published method.12 Male rats (6-week-old, weighing 150−160 g) were housed in a group of three and used as intruders. An intruder rat was placed in a resident’s home cage, and resident–intruder interactions were recorded using a video camera for 10 min. Resident rats subjected to social isolation stress showed aggressive behavior characterized by wrestling, boxing, and biting. Tail rattling, lateral threat, and pursuit were excluded. The time spent exhibiting aggressive behavior was measured during a 10 min observation period. This test was performed from 1:00 to 3:00 pm.

Plasma corticosterone levels

Levels of plasma corticosterone were measured to evaluate psychological stress.16 On day 8, rats were anesthetized using intraperitoneally administered pentobarbital sodium (50 mg/kg), and blood samples were taken from the inferior vena cava. All blood samplings were performed from 1:00 to 3:00 pm. Corticosterone levels were measured using an ELISA kit (ADI-900-097; Enzo Life Sciences, Farmingdale, NY, USA).

Influences of social isolation stress on orexin secretion

On day 8, levels of plasma orexins A and B (S-1148; Peninsula Laboratories International, San Carlos, CA, USA) were measured using ELISA kits. Next, orexin secretion in the lateral hypothalamus was determined using immunofluorescence analysis. After blood sampling, rats were exsanguinated by intracardial perfusion of phosphate-buffered saline (PBS) at pH 7.4. Rat brains were harvested after perfusion with 4% paraformaldehyde in 0.1 M PBS. Tissue specimens were embedded in optimal cutting temperature compound (Sakura Finetek Tissue-Tek, Tokyo, Japan), frozen, and then cut into 20 µm-thick sections using a cryostat (CM3050S; Leica Biosystems, Nussloch, Germany). Sections were incubated overnight at 4°C with a rabbit anti-orexin A antibody diluted 1:100 (PC362, Anti-Orexin A Rabbit Antibody; Merck, Darmstadt, Germany) and then incubated with Alexa Fluor 555-conjugated donkey anti-rabbit IgG secondary antibody diluted 1:1,000 (Thermo Fisher Scientific, Waltham, MA, USA) for 2 h at room temperature. Slides were mounted in Vectashield Antifade Mounting Medium (H-1000; Vector Laboratories, Burlingame, CA, USA) and imaged using a confocal laser scanning fluorescence microscope (FV1000D; Olympus, Tokyo, Japan). The optical densities of immunoreactive staining were measured using an appropriate software program (FV10-AW; Olympus). All values were reported as an average of four micrographs per rat. Background immunofluorescence was measured in the absence of primary antibody.

Involvement of orexin in stress responses

To determine whether orexin induces stress responses, 15 rats were randomly divided into groups of five as follows: 1) Con, 2) Stress, and 3) orexin receptor antagonist-treated stress (Stress + DORA). Rats in the Stress and Stress + DORA groups were individually housed for 8 days, and those in the Con group were housed in groups of two or three per cage. Rats in the Stress + DORA group were administered DORA (10 mg/kg) 1 h before the stress measurement on days 7 and 8, and those in the other groups were administered only 50% dimethyl sulfoxide. On day 7, an aggressive behavior test was performed,12 and on day 8, levels of plasma corticosterone were measured.

Statistical analysis

All experimental data are presented as mean ± standard error of the mean (SEM). Statistical significance of differences in the data was evaluated using one-way analysis of variance (ANOVA) test. Comparisons between the three groups were performed using the post hoc Tukey test. All P-values <0.05 were considered statistically significant.

Results

The administration of 300 mg/kg YKS for 7 days significantly decreased plasma orexin A level compared with that of the Con group (254.06±75.54 pg/mL vs 386.29±55.58 pg/mL, re spectively; P<0.05), whereas the administration of 1,000 mg/kg YKS did not (356.80±70.21 pg/mL; Figure 2). Therefore, an effective dose of 300 mg/kg YKS was administered to rats in subsequent experiments.

Figure 2

Plasma orexin A levels (pg/mL) following the administration of YKS.

Notes: Data are presented as mean ± SEM. Statistical analysis: one-way ANOVA followed by Tukey’s post hoc test, *P<0.05. Con, group-housed control.

Abbreviations: ANOVA, analysis of variance; SEM, standard error of the mean; YKS300, Yokukansan (300 mg/kg); YKS1000, Yokukansan (1,000 mg/kg).

On days 2 and 7, the 24 h food intake was measured. There rats were included in the Con group because seven rats were divided into three cages. On day 2, no difference was observed among the three groups. On day 7, the food intake in the Stress group (22.76±2.01 g) tended to increase with time, although this difference was not statistically significant compared with that in the Con group (21.51±0.84 g) and the Stress + YKS group (21.59±0.73; Figure 3A).

Figure 3

Effects of YKS on social isolation stress.

Notes: Food intake (g) (A), attack duration (s) in the resident–intruder test (B) and plasma corticosterone levels (ng/mL) (C). Data are presented as mean ± SEM. Statistical analysis: one-way ANOVA followed by Tukey’s post hoc test, *P<0.05, **P<0.01. Con, group-housed control; Stress, individually housed stress; Stress + YKS, individually housed YKS-treated stress.

Abbreviations: ANOVA, analysis of variance; SEM, standard error of the mean; YKS, Yokukansan.

On day 7, we measured the total duration of aggressive behavior during a 10 min observation. Rats in the Stress group exhibited significantly longer aggressive behavior compared with that of rats in the Con group (172.29±43.52 s vs 5.71±6.90 s, respectively; P<0.01); however, YKS administration significantly inhibited aggressive behavior (90.00±46.21 s, P<0.01; Figure 3B).

Plasma corticosterone level

On day 8, plasma corticosterone levels were measured as a marker of stress. Plasma corticosterone level significantly increased in the Stress group compared with that in the Con group (69.81±26.14 ng/mL vs 25.57±19.30 ng/mL, respectively; P<0.01); however, YKS administration significantly inhibited the elevation of corticosterone level in response to stress (31.49±19.54 ng/mL, P<0.05; Figure 3C).

Influence of social isolation stress on orexin secretion

On day 8, orexin A levels were significantly higher in the Stress group than in the Con group (530.09±31.86 pg/mL vs 343.52±137.67 pg/mL, respectively; P<0.05); however, YKS administration significantly inhibited the elevation in orexin A level (337.52±122.33 pg/mL, P<0.05; Figure 4A). Similarly, orexin B levels were significantly higher in the Stress group than in the Con group (538.57±92.60 pg/mL vs 442.99±28.25 pg/mL, respectively; P<0.05); however, YKS administration significantly inhibited the elevation in orexin B level in response to stress (432.55±68.89 pg/mL; P<0.05; Figure 4B). Orexin A and B secretion levels were similar.

Figure 4

Effects of YKS on social isolation stress.

Notes: Plasma orexin A (A) and B levels (pg/mL) (B). Orexin A (+) cell (red) in the lateral hypothalamus; magnification, ×200; scale bar =100 µm (C). The fluorescence density quantification of orexin A immune reactivity (D). Data are presented as mean ± SEM. Statistical analysis: one-way ANOVA followed by Tukey’s post hoc test, *P<0.05, **P<0.01. Con, group-housed control; Stress, individually housed stress; Stress + YKS, individually housed YKS-treated stress.

Abbreviations: ANOVA, analysis of variance; SEM, standard error of the mean; YKS, Yokukansan.

Immunohistochemical analysis revealed increased number of orexin A (+) cells in the lateral hypothalami of rats in the Stress group compared with the Con group (Figure 4C); however, this elevation in the number of cells was inhibited in the Stress + YKS group. The values were then expressed as optical densities (Figure 4D). Four images were recorded per rat, the immune reactivities were quantified, and all values were reported as an average of four micrographs per rat. The level was significantly increased in the Stress group (59.46±8.63 immunoreactive [IR] density) compared with that in the Con group (37.99±10.22 IR density; P<0.01). This increase was significantly inhibited in the Stress + YKS group (47.48±5.46 IR density; P<0.05). Overall, these findings indicate that YKS attenuates the enhancement of orexin secretion caused by social isolation stress.

DORA was administered to rats subjected to stress to investigate whether orexin was involved in stress responses. Rats in the Stress group exhibited aggressive behavior for significantly longer times compared with the Con group (179.00±60.29 s vs 11.80±16.44 s; P<0.01); however, the administration of DORA significantly inhibited aggressive behavior (55.20±47.99 s, P<0.01; Figure 5A).

Figure 5

Effects of TCS 1102, a DORA, on social isolation stress.

Notes: Attack duration (s) in the resident–intruder test (A) and plasma corticosterone levels (ng/mL) (B). Data are presented as mean ± SEM. Statistical analysis: one-way ANOVA followed by Tukey’s post hoc test, *P<0.05, **P<0.01. Con, group-housed control; Stress, individually housed stress; Stress + DORA, dual orexin receptor antagonist-treated stress.

Abbreviations: ANOVA, analysis of variance; DORA, dual orexin receptor antagonist; SEM, standard error of the mean.

Plasma corticosterone levels in the Stress group were significantly higher than those in the Con group (73.11±35.67 ng/mL vs 25.63±5.73 ng/mL, respectively; P<0.05); however, YKS administration significantly inhibited the elevation of corticosterone levels in response to stress (31.32±5.08 ng/mL, P<0.05; Figure 5B).

Discussion

YKS exerts therapeutic effects on the behavioral and psychological symptoms of dementia (BPSD) of elderly people with dementia,26 and therefore it has received much attention. YKS has been reported to have antistress,14,15 anxiolytic,27 and antihallucinatory effects.28 Furthermore, it ameliorates sleep disorders24,25 and cognitive dysfunctions;29 acts as a neuroprotective agent,30 and induces neuronal differentiation.31 YKS is also an analgesic21,22,32 that prevents the development of morphine tolerance,33 and it acts as an antipruritic34 and inhibits allergic responses34 and dyskinesia.23

YKS is an agonist of the serotonin receptor 5-hydroxytryptamine (5-HT)1A 27 and inhibits the expression of 5-HT2A receptors expressed by serotonergic and glutaminergic neurons in the central nervous system.28 Further, YKS inhibits the secretion of glutamate,35 enhances glutamate clearance from the extracellular fluid by astrocytes,36 and acts as an N-methyl-D-aspartate receptor antagonist.37 Moreover, YKS inhibits the activation of glial cells.32,33 However, to our knowledge, the effects of YKS on the interactions of orexin with components of the nervous system have not been previously reported. Therefore, in the current study, we investigated whether YKS has any influence on orexin secretion and whether the control of the interactions of orexin with the nervous system is involved in the antistress activity of YKS.

First, we administered YKS to rats that were not subjected to stress load for 1 week and then determined the effects of YKS on orexin secretion. The dose was determined according to the results of previous studies that administered YKS in the range of 50 mg/kg per day to 1,000 mg/kg per day,11–15,20–25 depending on the experimental model and animal species. Uchida et al,11 reported a stress load consistent with that of the current study and that 300 mg/kg of YKS was effective. In other experiments, YKS was administered at the upper limit of 1,000 mg/kg.14,15,20,21 In this study, we orally administered these two doses once each day. Plasma orexin A concentration in the 300 mg/kg YKS-treated group was significantly lower than that of the Con group after 1 week; however, no difference between the two groups was observed for a YKS dose of 1,000 mg/kg (Figure 1). In general, therapeutic actions of drugs approved, for example, by the regulatory agencies of North American and European countries, are unidirectional and they are characterized by sigmoid dose–response curves. In contrast, because Kampo medicines comprise several types of crude medicinals, and as described earlier, its constituents have numerous and diverse pharmacological actions, agonists and antagonists coexist, and certain dose–response curves are not sigmoidal but peak in the middle of the concentration ranges tested.22,38

Next, we investigated the effects of YKS on stress response using a rat model of social isolation. In the current study, we investigated changes in food intake, aggressive behavior, and plasma corticosterone levels. Similar to that reported by a previous study,18 the food intake on day 7 in the Stress group tended to increase with time, although the difference was not statistically significant compared with that in the Con group. The time to engage in aggressive behavior in the presence of intruders was significantly extended by subjecting the rats to social isolation stress load for 1 week. Herein, we show that corticosterone secretion significantly increased in response to stress and that this stress effect was significantly inhibited by the administration of YKS (Figure 3A–C).

Subsequently, we investigated whether this stress response was involved in the regulation of orexin secretion. In experiments using model animals of stress, the activation of orexin neurons in the lateral hypothalamic region was induced by constraint, cold temperature,39 and forced swimming.40 Further, intracerebroventricular administration of orexin increases the levels of ACTH and corticosterone.41 In contrast, systemic administration of orexin acts directly on the adrenal cortex and increases plasma corticosterone and aldosterone levels.42 Moreover, orexin receptors are present in the adrenal medulla,43 and orexin promotes the secretion of epinephrine.44 These findings provide compelling evidence that orexin plays an important role in the stress response via the HPA and SAM axes.

Findings of the current study reveal that the significant increase in orexin level induced by social isolation-related stress load was significantly inhibited by the administration of YKS (Figure 4A and B). Xiao et al45 reported that the orexin A immunoreactivity in the lateral hypothalamus increased in rats with stress induced by electric foot shocks and noises. In the current study model as well, the excitability of orexin neurons in the hypothalamus was higher than that in the Con group, and this phenomenon was diminished by the administration of YKS (Figure 4C and D). Orexins A and B are synthesized from the same precursor prepro-orexin, and their secretion levels are similar.4 In the current study, we detected elevated secretion of orexins A and B in response to stress loading, which could be inhibited via the administration of YKS. Orexinergic neurons are mainly expressed in the lateral and perifornical areas of the posterior hypothalamus; however, they were found in other organs, such as gut, stomach, and pancreas.46 Therefore, more detailed studies are needed to clarify whether the inductions of these stress responses and the antistress effects of YKS are associated with orexin secretion in the hypothalamus alone.

Finally, we investigated whether orexin was involved in the induction of stress response. There are two orexin receptor isoforms OX1R and OX2R.4 Administering a DORA to stress-loaded animals significantly inhibited aggression and increased plasma corticosterone levels, suggesting that orexin was involved in the induction of stress response. The differences, if any, in the actions of orexin A and B and OX1R and OX2R are unknown, but we plan to conduct experiments in the future to determine whether they have separate roles in the stress response. Our current findings suggest that orexin is involved in the induction of stress response to social isolation-related stress load and that YKS may exhibit its antistress effect through the regulation of orexin secretion. Because only aggressive behavior and plasma corticosterone level were investigated as stress responses in this study, further studies are necessary to elucidate the associations between other stress responses and orexin and the efficacy of YKS on them.

YKS comprises seven crude medicinals (Table 1). According to Kampo medical theory, of these seven crude medicinals, Bupleuri radix, Cnidii rhizoma, and Uncariae cum Uncis ramulus are used to stabilize the mind. Orexin neurons are inhibited by serotonin (5-HT), noradrenalin, and gamma-aminobutyric acid, and the action of 5-HT is transduced through the 5-HT1A receptor.4,47

YKS is an agonist of the 5-HT1A receptor, and evidence indicates that geissoschizine methyl ether, an alkaloid syn-thesized by Uncariae cum Uncis ramulus,20,27 mediates this activity. Accordingly, the action of Uncariae cum Uncis ramulus via the 5-HT1A receptor may represent one of the mechanisms through which YKS exerts its inhibitory effects on orexin neurons. Future studies are required to identify crude medicinals that regulate orexin secretion as well as their mechanisms.

Orexin neurons integrate information received from tissues, such as the limbic system, hypothalamus, and brain-stem, and adjust behavior and autonomic functions. Therefore, certain disorders of these autonomic functions are caused by malfunction of the orexin system. To the best of our knowledge, the current study is the first to investigate the effects of YKS on the regulatory action of the orexin system, and our findings will likely form the basis of future experiments that will help elucidate indications for using YKS.

Conclusion

Our findings suggest that orexin is involved in the regulation of some stress responses and that YKS exerts its antistress effect via the regulation of orexin secretion.