Desflurane anesthesia shifts the circadian rhythm phase depending on the time of day of anesthesia.

Desflurane is one of the most frequently used inhalational anesthetics in clinical practice. A circadian rhythm phase-shift after general anesthesia with sevoflurane or isoflurane has been reported in mice, but few studies have reported this effect with desflurane. In the present study, we examined the rest/activity rhythm of mice by counting the number of running wheel rotations, and we found that desflurane anesthesia caused a phase shift in the circadian rhythm that was dependent on the time of day of anesthesia. We also found that desflurane anesthesia altered the relative mRNA expression of four major clock genes (Per2, Bmal, Clock, and Cry1) in the suprachiasmatic nucleus (SCN). These results are important for elucidating the effects of desflurane on the SCN, which is the master clock for the mammalian circadian rhythm. Further studies on the relationship between anesthesia and circadian rhythm may lead to the prevention and treatment of postoperative complications related to circadian rhythms.

Introduction

The circadian rhythm is an innate ability in almost all living things. In mammals, the circadian rhythm master clock is in the suprachiasmatic nucleus (SCN), and it controls the circadian rhythm of behavior, circulation, and the endocrine system[1]. Circadian rhythm disorders may cause various diseases[2,3]. Postoperative sleep disorder is one of the most frequent symptoms caused by abnormal circadian rhythms[4]. Postoperative delirium and cognitive decline may also be associated with an abnormal circadian rhythm[5]. These symptoms decrease the quality of life of postoperative patients and their families and are also risk factors for other fatal complications[6,7]. Therefore, elucidating the mechanism of postoperative circadian rhythm disorder is clinically important.

Sevoflurane, isoflurane, and desflurane are the most commonly used inhalational anesthetics in clinical practice. General anesthesia with sevoflurane or isoflurane affects the circadian rhythm by altering clock gene expression in the SCN[8,9]. Furthermore, previous reports suggested that the effect of sevoflurane and isoflurane anesthesia on the circadian rhythm might differ depending on the time of day of anesthesia[10,11]. However, the effects of desflurane general anesthesia on the circadian rhythm have not been reported. Desflurane has a significantly lower solubility in blood compared with other volatile anesthetics and is eliminated through exhalation without being metabolized. These characteristics contribute to the rapid onset and offset of desflurane anesthesia, and in fact, anesthesiologists often administer desflurane as general anesthesia to quickly wake patients after surgery. Based on these characteristics, desflurane might have a different effect on the circadian rhythm compared with other inhaled anesthetics[12].

The circadian clock is an endogenous mechanism that controls 24-h physiological processes through a transcriptional feedback loop of clock genes. Recent studies have identified many important clock genes involved in regulating the circadian clock in mammals. Among them, Period (Per), Bmal, Clock, and Cryptochrome (Cry) are the most well-known and particularly important clock genes for the formation of the circadian rhythm. Entrainment of the circadian clock in mammals mainly depends on light stimuli, which are received by intrinsically photosensitive retinal ganglion cells (ipRGCs) and inputted into the SCN via the retinohypothalamic tract (RHT)[13]. Nonphotic entrainment in mammals has also been studied. Exercise, mealtime, social contact, and pharmacological compounds are known to have chronobiotic potential[14]. In recent studies, anesthetics have been investigated as drugs with chronobiotic potential. Volatile anesthetics, such as sevoflurane, epigenetically suppress Period2 transcription by inhibiting the acetylation of the Period2 promoter, thereby causing a phase shift in the circadian rhythm of mice[15]. In addition, the recovery time from sevoflurane and isoflurane anesthesia is different in the circadian phase, and it involves the locus coeruleus noradrenergic system[16]. However, there is limited information regarding the effects of desflurane on the circadian rhythm and clock gene expression. In addition, whether the effects of desflurane are dependent on the time of day of anesthesia is poorly understood.

In this study, we quantitatively evaluated the effect of desflurane anesthesia on the circadian rhythm by monitoring the rest/activity rhythm in mice and examining its dependence on the time of day of anesthesia. In addition, to determine the effect of desflurane anesthesia on the master clock, the expression of four major clock genes in the SCN was measured.

Materials and methods

Animal preparation

Experiments were conducted in accordance with guidelines approved by the Animal Care Committee of the Hamamatsu University School of Medicine Animal Care Facility. Adult (6–8 weeks old, mean body weight ± SD of 20.9 ± 1.4 g) male C57BL/6 J mice (SLC, Hamamatsu, Japan) were used for all experiments.

Mice were housed for at least 10 days to allow adaptation to the light:dark conditions (LD), which consisted of a 12-h light (from zeitgeber time [ZT]0 to ZT12) and 12-h dark (from ZT12 to ZT24) cycle. ZT is a chronobiology term, and ZT12 indicates the beginning of the dark phase under LD. Food and water were available ad libitum.

Anesthesia

Mice were placed in a small chamber for anesthesia using 4% desflurane (0.52 MAC (minimum alveolar anesthetic concentration)[17]), which was initiated with a 4 L/min flow of 50% oxygen. After anesthesia induction, the fresh gas flow was decreased to 1 L/min. The anesthetic chamber was placed on a heated plate to maintain normal body temperature in the mice. Anesthesia was performed for 6 h[11]. These procedures were performed under dark conditions, and a dim red light that did not affect the circadian rhythm was used as needed.

Rest/activity rhythm phase shift measurements

Seventy-two mice were used for this experiment. A commercially available mouse running wheel was used to monitor the rest/activity rhythm of mice. We set the magnetometric sensor behind the wheel embedded magnets and used a self-made device and software to count the wheel rotations. The rest/activity rhythm of mice was recorded automatically from the beginning to the end of the experiment.

After adaptation with the running wheel, the dark conditions (DD; constant dark conditions) were initiated on day 1. Mice were divided into two groups (n = 36 per group). One group was anesthetized with desflurane under DD conditions on day 5. The other group was not anesthetized but was placed in the anesthetic chamber and then back into its cage. The two groups were each divided into six subgroups (ZT0, ZT4, ZT8, ZT12, ZT16, and ZT20; n = 6 per subgroup) based on the anesthetic procedure time of day (Fig. 1).

Figure 1

Rest/activity rhythm phase shift measurements in mice. LD started more than 10 days before the initiation of DD. The light phase was from ZT0 to 12 in LD. Anesthesia was performed on DD day 5 (left), and mice were divided into 6 subgroups according to the time-of-day of anesthesia (right; n = 6 per subgroup). In the group without anesthesia, the same procedure was performed when anesthesia was started. The time at the beginning of the active phase in mice (thick line) was determined from the actogram, and the time on DD day 6 was estimated. The difference from the estimated and actual beginning time of the active phase on DD day 6 was defined as the phase shift after anesthesia.

After the anesthetic procedure, the mice were placed back into their original cages. Their rest/activity rhythm was monitored for more than 6 days after the anesthetic procedure. We evaluated the phase shift, which is the difference between the actual and predicted start time of day for the active phase on the day after anesthesia (Fig. 1). We also evaluated the circadian period for each group.

SCN sample collection

Samples were collected from 48 mice. After adaptation, DD conditions were initiated on day 1. Mice were divided into two groups (n = 24 per group). The anesthesia group was exposed to 4% desflurane for 6 h, and the SCN sample was collected immediately after anesthesia. The other group did not undergo desflurane anesthesia before the SCN was collected. The two groups were each divided into six subgroups based on the time of day at which the sample was collected (n = 4 per subgroup). Samples were collected at ZT0, ZT4, ZT8, ZT12, ZT16, and ZT20 on day 1 (Fig. 2). Sample collection was performed under dim red light. Mice were euthanized by cervical dislocation. The brain was quickly removed within a few minutes and placed into RNAlater (Qiagen, Hilden, Germany). The brain was immediately cut with a brain slicer (Muromachi Kikai, Tokyo, Japan) into sections (1.5 mm thick), which included the SCN. The bilateral SCN was resected as a triangular prism (~ 2 mm a side) using micro scissors in RNAlater reagent and placed into a collection tube with fresh RNAlater (150 µl). These processes required only about 15 min. The collected samples were stored at 4ºC for approximately 1 week until RNA extraction and reverse transcription.

Figure 2

Protocol for SCN sampling in mice. After adaptation, anesthesia was performed on DD day 1. Mice were divided into 6 subgroups according to the time-of-day of anesthesia (n = 4 per subgroup). SCN sampling was performed at the end of anesthesia. In the group without anesthesia, SCN sampling was performed at the same time without anesthesia.

Quantitative real-time polymerase chain reaction (q-PCR)

Total RNA was extracted from the collected SCN samples using an RNeasy Mini Kit (Qiagen). The RNA was reverse transcribed into cDNA using a QuantiTect Reverse Transcription Kit (Qiagen). q-PCR was performed using a StepOnePlus Real-Time PCR system (Applied Biosystems, Foster, CA, USA) and QuantiTect SYBR Green PCR Kit (Qiagen). Target gene expression was quantified using the ΔΔCt method.

The target clock gene primers were as follows: Per2 forward primer, 5′-ATCAGCCATGTTGCCGTGTC-3′ and Per2 reverse primer, 5′-CGTGCTCAGTGGCTGCTTTC-3′; Bmal forward primer, 5′-ACGACATAGGACACCTCGCAGA-3′ and Bmal reverse primer, 5′-TCCTTGGTCCACGGGTTCA-3′; Clock forward primer, 5′-AGCTGCATATTGCCGTTGTAATTG-3′ and Clock reverse primer, 5′-CTGAGTGAAGGCATGCTGGTG-3′; and Cry1 forward primer, 5′-GGATCCACCATTTAGCCAGACAC-3′ and Cry1 reverse primer, 5′-CATTTATGCTCCAATCTGCATCAAG-3′.

The internal control gene primers were as follows: Actb forward primer, 5′-CATCCGTAAAGACCTCTATGCCAAC-3′ and Actb reverse primer, 5′-ATGGAGCCACCGATCCACA-3′.

The protocol for q-PCR consisted of three stages. The holding stage kept the temperature at 95 °C for 15 min; the cycling stage repeated 40 cycles of 94 °C for 15 s and then 58 °C for 1 min; and the melt curve stage was confirmed by 95 °C for 15 s and 60 °C for 1 min, followed by increasing the temperature in increments of 0.3–95 °C for 15 s.

Statistical analysis

To determine the statistical difference in the phase shift and circadian period between desflurane-anesthetized mice and controls, a Mann–Whitney U-test was applied. Time-dependent fluctuations in the phase shift and relative changes in gene expression were analyzed using the Kruskal–Wallis test followed by the Mann–Whitney U-test, and the p value was adjusted by Bonferroni correction. All statistical analyses were performed using R (version 3.3.2), and p values < 0.05 were considered statistically significant.

Results

Phase shift of rest/activity rhythm after desflurane anesthesia

A total of 72 mice were used to measure the phase shift after desflurane anesthesia, and no mice were excluded during measurements. A representative double-plot actogram shows the phase delay in mice after desflurane anesthesia from ZT6 to ZT12, but there was no phase shift in the non-anesthetized mice (Fig. 3). The number of running wheel rotations obtained from each mouse was determined in 10-min intervals to generate a bar graph in which 48 h are shown in one line.

Figure 3

Representative double-plot actogram in mice. The number of running wheel rotations obtained from each mouse was determined in 10-min intervals to generate a bar graph in which 48 h are shown on one line. This anesthesia (+) mouse showed a phase shift of − 1.45 h, and the anesthesia (−) mouse showed no phase shift.

The circadian time, phase shift, and circadian period of rest/activity rhythm in each subgroup in both groups are shown in Table 1. The largest phase shift was observed in the ZT12 subgroup of the anesthesia group, and there was a significant difference between the anesthesia and non-anesthesia groups (− 1.69 h vs. − 0.58 h, p = 0.005). A significant difference in the phase shift was also observed between subgroups ZT4 and ZT12 (0.46 h vs. − 1.7 h, p = 0.032) and between subgroups ZT4 and ZT20 (0.46 h vs. − 1.1 h, p = 0.032) in the anesthesia group.

Table 1

Circadian time, phase shift, and circadian period of the rest/activity rhythm in mice. Circadian time is the subjective time of each mouse at the time-of-day of anesthesia. Phase shift (h) is the difference between the actual and predicted start time of day for the active phase on the day after anesthesia. Circadian period (h) of DD days 1–4 and DD day 6– indicate the circadian period before or after the anesthetic procedure in mice. The median (Interquartile range) of the circadian time, phase shift, and circadian period was calculated for each subgroup (n = 6). The p value was calculated using the Mann–Whitney U-test.

Group	Anesthesia (+), n = 36
Subgroup	ZT0 (n = 6)	ZT4 (n = 6)	ZT8 (n = 6)	ZT12 (n = 6)	ZT16 (n = 6)	ZT20 (n = 6)
Circadian time	2.0 (1.7–2.3)	5.1 (5.0–6.5)	10.3 (9.5–10.4)	15.0 (14.6–15.3)	18.2 (17.9–18.6)	23.3 (21.7–23.9)
Phase shift (h)	− 0.21 (− 0.44 to − 0.10)	0.46 (0.15–0.65)*,**	− 0.71 (− 0.83 to − 0.58)	− 1.7(− 1.8 to − 1.5)*,***	− 0.75(− 1.1 to − 0.33)	− 1.1(− 1.5 to − 0.77)**
Circadian period (h)
LD	23.96 (23.96–23.96)	24.00 (23.96–24.04)	24.02 (23.97–24.04)	24.02 (23.97–24.04)	23.98 (23.96–24.04)	24.00 (23.96–24.04)
DD day 1–4	23.59 (23.54–23.66)	23.77 (23.50–23.79)	23.54 (23.51–23.70)	23.40 (23.35–23.48)	23.56 (23.48–23.61)	23.33 (23.22–23.67)
DD day 6–	23.69 (23.64–23.80)	23.76 (23.62–23.82)	23.79 (23.66–23.79)*,***	23.67 (23.56–23.77)	23.62 (23.61–23.78)	23.65 (23.50–23.79)

Median (interquartile range).

Phase shift (h): *subgroup ZT4 versus ZT12, p = 0.03, **subgroupZT4 versus ZT20, p = 0.03, ***anesthesia (+) versus (−) in subgroupZT12, p = 0.005.

Circadian period DD day 6–: ****anesthesia (+) versus (−) in subgroupZT8, p = 0.01.

The median phase shift was delayed for − 0.67 h [interquartile range (IQR), − 1.27 to − 0.15] in the anesthesia group and − 0.33 h (IQR, − 0.67 to 0.02) in the non-anesthesia group (p = 0.043).

The phase shift in all mice that showed a different circadian time of the anesthetic procedure was shown in Fig. 4. Fluctuations in the extent of the phase shift were observed in mice after desflurane anesthesia (p = 0.00037), but these were not observed in non-anesthetized mice (p = 0.17; Fig. 4).

Figure 4

Double-plot of the phase shift based on the circadian time of anesthesia. The phase shift of all mice was plotted against the circadian time of anesthesia [left, anesthesia (+); right, anesthesia (−)].The solid line indicates the median phase shift (h), and the broken lines show the interquartile range (IQR) against the median circadian time of anesthesia in each subgroup (n = 6).

The circadian time of the anesthetic procedure was calculated based on the circadian period before the anesthetic procedure. There was no statistically significant difference in the changes in circadian time between the anesthetized group, the non-anesthetized group, and each subgroup. The circadian period in all mice that showed a different circadian time of anesthesia was shown in Fig. 5. The circadian period was different in each mouse, but no significant difference was observed between the anesthesia and non-anesthesia groups. Within each subgroup, only ZT8 showed a significant difference in the circadian period in DD after the anesthetic procedure (p = 0.01) (Table 1).

Figure 5

The circadian period under DD conditions in all mice. DD days 1–4 and DD day 6– indicate the DD condition before and after the anesthetic procedure, respectively. All circadian periods in the DD condition were plotted against the circadian time of the anesthetic procedure. The anesthesia (+) group is on the left, and the anesthesia (−) group is on the right. The solid and broken lines are the median and IQR of the circadian period, respectively, calculated in each subgroup.

Changes in the relative expression level of clock genes after desflurane anesthesia

A total of 48 mice were used to measure the relative expression level of clock genes after desflurane anesthesia. No mice were excluded. The relative expression level of clock genes was calculated by dividing the gene expression in anesthetized mice by that of non-anesthetized mice. The calculation was performed in groups of samples that were collected at the same time of day. Therefore, the original circadian variation in clock gene expression was excluded. The relative expression level of each clock gene differed depending on the time of day of anesthesia (Per2: p = 0.042, Bmal: p = 0.011, Clock: p = 0.0023, Cry1: p = 0.024; Fig. 6). Bmal and Cry1 expression levels were increased in subgroup ZT12 [Bmal: 1.87 (IQR, 1.95–1.82) and Cry1: 2.18 (IQR, 2.54–1.85)]. However, Clock expression was decreased after anesthesia at the same time of day [Clock in subgroup ZT12: 0.36 (IQR, 0.37–0.30)]. Additionally, Per2 expression increased after anesthesia from ZT2 to ZT8 [Per2: 2.67 (IQR, 2.86–2.22].

Figure 6

Relative mRNA expression level of clock genes in the SCN after anesthesia. The relative expression level of Per2, Bmal, Clock, and Cry1 was measured as indicated in the left upper corner of each graph. The relative expression level was calculated by dividing the mRNA expression of the anesthesia group by that of the non-anesthesia group in each subgroup. The calculation was performed in groups in which the SCN was collected at the same time of day. The mRNA expression was measured by q-PCR using the ΔΔCT method. The p value was calculated using the Kruskal–Wallis test. Error bars indicate the standard deviation.

Discussion

Desflurane anesthesia shifted the rest/activity rhythm phase in mice, and the extent of the phase-shift differed depending on the time of day of anesthesia. The effects of inhaled anesthetics on the circadian rhythm have been reported for sevoflurane and isoflurane[8,9]. During the active or inactive phase, 2.5% of sevoflurane anesthesia delayed the phase of rest/activity rhythm and suppressed Per2 expression in the mouse SCN[18]. Similarly, during the active period, 1% isoflurane anesthesia shifted the rest/activity rhythm and disturbed acetylcholine release in the rat hippocampus[9]. However, previous studies have not quantitatively investigated the influence of the time of day of anesthesia. In the present study, the phase delay was largest after anesthesia in ZT6–12, which is the latter half of the inactive phase. However, desflurane anesthesia was performed on day 5 after DD was initiated. The circadian period of mice under DD is known to be 23.28–23.77 h[19], which is similar to our result (Table 1). Therefore, when desflurane anesthesia was performed on day 5, the beginning of the active phase was estimated to have advanced by 2.5 h. In fact, the median circadian time of subgroup ZT12 was 15.0 in the anesthesia group and 14.4 in the non-anesthesia group. Desflurane anesthesia in ZT6–12, which showed the largest phase shift, involved anesthesia administration from the late inactive phase to the early active phase subjectively in mice. Previous studies using isoflurane indicate that anesthesia at the beginning of the active phase causes a large delay in the phase shift[20], which is consistent with our findings.

In addition, the effect of anesthesia at the beginning of the active phase on enhancing the phase delay is similar to the effect of light pulses at the beginning of the active phase that delays the circadian rhythm in nocturnal animals[21]. In mammals, light stimuli received by ipRGCs are transmitted to the SCN via the RHT[14]. Glutamate, pituitary adenylate cyclase activating polypeptide (PACAP), and aspartate are the neurotransmitters of signals from the RHT to the SCN, and glutamate plays the most important role among them. Inhaled anesthetics, including desflurane, act as an N-methyl-d-aspartate (NMDA) receptor antagonist, which competitively inhibits glutamate transmission. Blocking the input signal from the RHT to the SCN might cause a phase shift[22,23]. However, each anesthesia procedure was performed under DD in our study. Whether inhaled anesthetics time-dependently suppress the input signal from the RHT, even under dark conditions, remains unknown.

It has been reported that desflurane has different effects compared with other inhaled anesthetics on melatonin production after daytime anesthesia[13]. The sympathetic system regulates melatonin synthesis by β1 and α1 adrenergic receptor activation[24,25]. Melatonin is an endocrine hormone secreted by the pineal gland, which is under the control of the SCN circadian rhythm, and it is involved in the rest/activity rhythm of many mammals[26]. The sympathomimetic effect induced by desflurane might have influenced the original circadian rhythm through sympathetic activity[27]. Because C57BL/6 J mice do not produce melatonin, melatonin is irrelevant in the interpretation of these results. However, the sympathomimetic effect may explain why desflurane showed a significant time-dependent fluctuation in the phase shift, unlike sevoflurane.

The effects of general anesthesia on clock genes have been increasingly elucidated in recent years. Sevoflurane anesthesia suppresses Per2 expression in the SCN, and it is related to the epigenetic regulation of clock genes[16]. Additionally, isoflurane anesthesia advances the circadian rhythm in mice, and this is related to increased Bmal expression[9]. We investigated the expression of four clock genes (Per2, Bmal, Clock, and Cry1) after desflurane anesthesia using real-time PCR. Bmal and Cry1 showed increased expression with the peak observed after ZT6–12 anesthesia. However, Clock expression was most suppressed after anesthesia at the same time of day. Per2 expression showed no significant change after ZT6–12 anesthesia, but it increased after ZT2–8 anesthesia. The SCN is the master biological clock in mammals. The rest/activity rhythm is regulated by the dorsomedial hypothalamic nucleus and the locus coeruleus, which have a circadian rhythm that is synchronized with the circadian oscillation of the SCN[28]. In our study, the phase shift in the rest/activity rhythm was enhanced after anesthesia from ZT6 to ZT12. The change in the relative expression level of clock genes was also enhanced after anesthesia at the same time of day. Clock gene expression is feedback-regulated by the levels of other clock genes and proteins. BMAL and CLOCK proteins bind to a region termed the E-box and promote the transcription of Per2[29,30]. The transcribed and translated PER protein binds to CRY and exerts negative feedback on its transcription[31,32]. Increased Bmal expression after ZT6–12 anesthesia was thought to have resulted in increased Cry1 expression after anesthesia at the same time of day. However, Clock expression decreased reciprocally after ZT6–12 anesthesia compared with the increase in Cry1 expression. Desflurane anesthesia altered the expression of each clock gene in the SCN, and this effect was dependent on the anesthesia time of the day. However, the molecular mechanisms regulating the circadian clock in the SCN are complicated, and it was difficult to determine the meaning of each alteration.

Clock expression was originally reported to have no circadian oscillation in the SCN. CLOCK is a histone acetyltransferase that forms a heterodimer with BMAL1 and promotes the transcription of Per and Cry mRNA via the E-box in their promoters. This is an important mechanism controlling the transcription and translation feedback loop of clock genes[33]. In fact, mice with mutant Clock genes show a prolonged circadian rhythm[34]. In our study, desflurane anesthesia showed a time-dependent effect on the relative mRNA expression level of Clock, and it was significantly decreased after ZT6–12 anesthesia. Because Clock shows no circadian variation in mRNA expression in the SCN, the decrease in the relative gene expression of Clock indicates that desflurane either directly or indirectly suppressed its expression. It is possible that decreased Clock expression slowed down the clock gene feedback loop and delayed the circadian rhythm phase. Further experiments are required to investigate the mechanisms by which anesthetics alter Clock gene expression.

In clinical practice, postoperative delirium, cognitive decline, and sleep disorders have been suggested to be associated with circadian rhythm disorders[35]. Many researchers suggest that general anesthetics may influence the development of these postoperative complications through altered clock gene expression in the SCN. Clinical applications of chronobiology have begun to be adopted in intensive care units[36]. However, the mechanisms of complications caused by the destructed circadian rhythm by anesthetics remain mostly unclarified. Based on our findings, the frequency of postoperative delirium, cognitive decline, and sleep disorders might differ depending on when the patients have surgery under inhalational anesthesia. Further clinical investigations examining the association between the time of day of anesthesia and postoperative adverse events are needed to validate this hypothesis.

There are several limitations to the present study that should be highlighted. First, anesthesia was performed using a relatively low inhaled desflurane concentration of 4%, which is about 0.52 MAC for C57BL/6 J mice[12]. Prolonged anesthesia using a high concentration of desflurane is harmful because of its respiratory irritation and circulation suppression[27]. To maintain a normal rest/activity rhythm, it was necessary to maintain anesthesia without invasive procedures to protect the airway and circulation. Thus, we must reconsider the experimental methods to understand the phase shift of mice after deeper or longer anesthesia.

In addition, in the phase shift experiment, mice were anesthetized on DD day 5. However, to quantify clock gene expression, mice were anesthetized on DD day 1. This is because each mouse has a different circadian period. Clock gene expression varies because of the individual circadian rhythms, even when we collected SCN samples at the same time on DD day 5. The individual difference in circadian rhythms at the time of SCN collection was minimized by performing anesthesia on DD day 1. Therefore, the fluctuation in clock gene expression caused by desflurane anesthesia could be measured.

Finally, mice were anesthetized with 4% desflurane for 6 h. In previous studies, the duration of anesthesia was different and ranged from 30 min to 8 h. Anesthesia for 6 h was relatively long and might mitigate the difference between subgroups. However, the amplitude of phase response curves yields the maximum for a 9-h light pulse[37]. Therefore, the anesthesia for 6-h might not have been too long to mitigate the difference of subgroups.

In conclusion, the circadian rhythm measured by the rest/activity rhythm of mice showed a phase shift after desflurane anesthesia, and the extent differed depending on the time of day of anesthesia. The phase shift was largest in the latter half of the inactive phase. Desflurane anesthesia increased the mRNA expression of four major clock genes in the SCN, and these alterations after anesthesia also differed depending on the time of day of anesthesia. Although further clinical investigations are needed, our findings might suggest that the time at which patients have surgery under inhalational anesthesia is an important factor to maintain the circadian rhythm, even when using desflurane, which enables fast-track anesthesia in clinical practice.