What this is
- This research examines the expression of circadian clock genes in human adipose tissue.
- It investigates how , specifically dexamethasone (DEX), influence these gene expressions.
- The study focuses on visceral and subcutaneous fat from morbidly obese women.
Essence
- CLOCK, BMAL1, and PER2 genes exhibit circadian expression patterns in human adipose tissue. DEX alters these patterns, reducing their rhythmicity.
Key takeaways
- CLOCK, BMAL1, and PER2 show significant circadian rhythms in both visceral and subcutaneous adipose tissue, confirmed by statistical analysis.
- DEX exposure disrupts the normal circadian rhythms of these clock genes, shifting their expression patterns to approximately 12-hour cycles.
- The phase relationship between CLOCK and PER2 differs in subcutaneous vs. visceral fat, indicating distinct regulatory mechanisms.
Caveats
- All samples were from morbidly obese women, limiting generalizability to other populations, including non-obese individuals.
- The absence of a non-obese control group complicates the interpretation of glucocorticoid effects on clock gene expression.
Definitions
- circadian rhythm: Biological processes that display an endogenous, entrainable oscillation of about 24 hours.
- glucocorticoids: A class of steroid hormones that regulate various physiological processes, including metabolism and immune response.
AI simplified
Introduction
Circadian rhythmicity is essential to accommodate our physiology to the specific needs of the organism during the 24-hours day cycle. Mammalian circadian rhythms are regulated and synchronized by a master clock located in the hypothalamic suprachiasmatic nuclei (SCN) [1]. In addition, peripheral clocks that maintain circadian oscillations even in the absence of the master clock have been identified in other organs such liver, digestive system or even the adipose tissue (AT) [2], [3].
The first characterized clock component was the transcription factor CLOCK (Circadian Locomotor Output Cycles Kaput) [4] that dimerizes with BMAL1, another component of this system and constitutes the positive limb of the clock [1]. On the other hand, PER2 together with CRY1 constitutes the negative limb in this complex circadian machinery.
CLOCK is the product of the CLOCK gene that in both, genetic and experimental studies has been associated with obesity. Indeed, Clock mutant mice have been shown to be hyperphagic and obese relative to their wild-type controls [5]. Its deficiency was accompanied by alterations in diurnal rhythms of physical activity, feeding, and metabolic rate [5]. Similarly, in humans, a number of single nucleotide polymorphisms (SNPs) in Clock have been correlated with predisposition to obesity [6]–[8], and resistance to weight loss [9].
Previously, we have shown that PER2 and BMAL1 together with other genes coding for clock components (i.e., CRY1) are expressed in cultured human adipose tissue explants according to a rhythmic pattern [3]. However, it remains to be defined whether CLOCK exerts a similar circadian oscillation in human adipose tissue, and if this oscillation differs between visceral and subcutaneous fat depots.
A variety of biochemical factors, including glucocorticoids (GCs), have been shown to have the potential to alter transcription of core clock genes [10]. GCs have potent physiological effects and their levels show marked daily oscillation, which is thought to be driven by the master circadian clock in SCN of the hypothalamus via the hypothalamo-pituitary-adrenal axis [11]. These circadian oscillations are also present in human adipose tissue [3]. GCs bind to glucocorticoid receptors in the cytoplasm of target cells and then the glucocorticoid receptors are transported to the nucleus to act as transcription factors [11]. A relevant question is the potential influence of GCs on clock genes expression. In this sense, although it has been described that GCs are particularly potent at eliciting the rhythmic expression of the mRNAs for peripheral clock genes [11], outcomes remain controversial depending on the tissue and the clock gene studied. In human adipose tissue it has been described that GCs, particularly dexamethasone (DEX) generates circadian gene expression patterns in different clock genes in undifferentiated and adipocyte-differentiated stem cells [12]. In this context, the possible effect of GCs on CLOCK, BMAL1 and PER2 as representative genes of the positive and negative limb of the peripheral clock genes expression in human adipose tissue cultured remains unknown.
Therefore, the primary aims of this study were to characterize for the first time the rhythmicity of expression of CLOCK in human visceral and subcutaneous adipose tissue as compared with PER2 and BMAL1, and whether the glucocorticoid analogue DEX modulated positive and negative clock genes in vitro.
Subjects and Methods
Subjects
Visceral and subcutaneous abdominal adipose tissue biopsies were obtained from morbid obese non diabetic women (n = 6), aged 44±4 years and body mass index (BMI): 41.2±3.8 Kg/m2, undergoing laparoscopic gastric bypass surgery due to obesity at the General Surgery Service of “Virgen de la Arrixaca” Hospital (Murcia, Spain). The women studied were postmenopausal and were not under hormone replacement therapy. The day before surgery, all patients were synchronized having lunch at 14:30 h and dinner at 21:00 h. The adipose tissue biopsies were taken as paired samples from the two adipose tissue depots (visceral and subcutaneous) at the beginning of the surgical procedure (estimated time of biopsies sampling at 13:00 h).
The protocols were approved by the Ethics Committee of the “Virgen de la Arrixaca” University Hospital, and the subjects signed a written informed consent before the biopsies were obtained.
Clinical characteristics
Arterial pressure, BMI, waist and hip circumference were assessed by standard procedures, while skinfolds (biceps, triceps, suprailiac and subscapular) were measured with a Harpenden caliper (Holtain Ltd, Bryberian, Crymmych, Pembrokeshire, UK). Total body fat (%) was evaluated by bioimpedance with a TANITA TBF-300 (TANITA Corporation of America, Arlington Heights, IL). Sagittal diameter and coronal diameter were measured at the level of the iliac crest (L4–5) using a Holtain Kahn Abdominal Cali skinfold. Women were classified in visceral and subcutaneous obesity calculating the index VA/SA (Visceral Area/Subcutaneous Area) after applying the following equation [13]: VA/SApredicted = 0.868+0.064×Sagittal diameter – 0.036×Coronal diameter – 0.022×triceps skinfold. Those patients with VA/SA >0.42 were classified as having visceral obesity [13]. Fasting plasma concentrations of glucose, triacylglycerols, total cholesterol, low-density lipoprotein (LDL) cholesterol and high-density lipoprotein (HDL) cholesterol were determined with standard analytical methods (Roche Diagnostics GmbH, Mannheim, Germany). Basal metabolic Rate (BMR) was calculated from the Harris and Benedict equation [14].
Adipose Tissue Culture
Immediately after the surgery, explants were placed at 37°C for 24 hour in a humidified atmosphere containing 7% CO2 in culture dishes with 12 wells. Approximately 500 mg adipose tissue explants (minimal pieces of 1–2 mm3 in order to allow the maximal contact of adipose tissue with the medium) were placed in 2.5 ml of Dulbecco's modified Eagles Medium (DMEM) supplemented with 10% fetal bovine serum (GIBCO) and a mixture of penicillin-streptomycin-glutamine (PSG from GIBCO #10378-016).
On the next day, at 08:00 h a.m., the medium was exchanged with DEX medium (DMEM+PSG, supplemented with 1 µM DEX (0.4 mM in ethanol) (Brunschwig AG, Basel, Switzerland)). In control wells, a control medium 0.25% ethanol in DMEM with PSG was added. After 2 hours, at 10:00 h a.m., these mediums (DEX and control) were replaced with serum-free DMEM+PSG. Then, the adipose explants were collected to perform gene expression analysis at the following times (T): 0, 4, 8, 12, 16 and 20 in which T0 was arbitrarily defined as 10:00 h, T4 as 14:00 h, T8 as 18:00 h, T12 as 22:00 h, T16 as 02:00 h, and T20 as 06:00 h. Gene expression was measured only for one circadian cycle (24 hours), but in the second day of culture. All cultures were performed in duplicate.
Analysis of Gene Expression
Total RNA was extracted from adipose tissue explants using RNeasy Kit (QIAGEN, Courtabeouf, France). Reverse transcription was performed using random hexamers as primers and Thermoscript® reverse transcriptase (Invitrogen, Cergy Pontoise, France) with 1 µg total RNA for each sample. Quantitative real-time PCR was performed using an ABI PRISM 7000 HT Sequence Detection System (Applied Biosystems, CA, USA), using TaqMan® Universal PCR Master Mix and specific TaqMan probes (Applied Biosystems, CA, USA). The primers used in the study are the following references from Applied Biosystems: CLOCK (Hs00231857_m1), BMAL1 (Hs00154147_m1) and PER2 (Hs00256143_m1) and 18S (Hs99999901_s1). 18S was selected as the housekeeping gene because, as analyzed by repeated measures ANOVA test, no significant differences in circadian rhythmicity in 18S gene expression were observed in any of the fat depots studied among times (P>0.05). Gene mRNA levels were normalized to 18S using the 2−ΔΔCt method [15].
Rhythm Calculation and Statistical Analysis
Clinical and anthropometric data are presented as means ± SD. The results for gene expression, expressed in arbitrary units, are presented as means ± SEM.
To investigate the presence of circadian rhythms, least squares periodic regression [16] was used to fit the data, from each group, to a sinusoidal function. This adjustment allows verifying the presence of a circadian rhythm through the significance of fitting and the percentage of variance explained by the rhythm. It also provides the estimation of the characteristic parameters of the rhythm: the amplitude of oscillation, its acrophase (the time the variable reaches the maximum) and the central value (mesor). These parameters are represented graphically in a polar plot (hourly) to visualize the characteristics of the rhythm by a vector (cosinor) whose length corresponds to the amplitude and the direction to the acrophase.
All the data from all individuals are used simultaneously to directly estimate the population parameters (one-step method) using a model that includes a sinusoid and a constant for each individual, which corresponds to the individual mesor, eliminating the effect of interindividual variation in the estimated global rhythm. Confidence intervals of estimated parameters are narrower than in the two-steps method and the estimation of these parameters is more reliable.
The percentages of variance explained by the rhythm are referred to the “corrected variance”, after removing the effect of the mesor. Since in the dexamethasone treated group, the presence of a circadian rhythm was not detected, to investigate shape changes on the daily pattern, we used (in addition to T = 24 h) a sinusoidal function with T = 12 h. This curve is simply a bimodal pattern that produces a depression in the profile of the curve. This pattern fits remarkably well to the profile observed in the experimental results. Thus the sinusoid, with T = 12 h is a good mathematical model to fit the experimental points, without necessarily be interpreted as the presence of a rhythm of 12 h. In this case, the analysis and calculations follow the same steps as in the case of 24 hours, but changing the period. All calculations were performed with an “ad hoc” computer application (“Ritme v4”, @ Antoni Diez-Noguera, Univ. Barcelona, 2012) written in C++ and tested with examples from literature.
Mean circadian gene expression of the total population into each fat depot was analyzed by using repeated measures ANOVA test, with a post hoc test of least significant difference (LSD) correction and while differences in PR (Percent Rhythm: percentage of variability accounted for by sinusoidal curve) among control and DEX treated adipose explants from CLOCK and PER2 was analyzed by Wilcoxon non-parametric test. Statistical analysis (ANOVA, means, comparisons, etc) was carried out using the package SPSS for Windows (release 15.0; SPSS Inc, Chicago, US). The level of significance for all statistical tests and hypotheses was set at P<0.05.
Results
Characteristics of the Population
The women studied were morbidly obese (BMI>40 Kg/m2), non diabetic and they had MetS (Table S1 contains baseline characteristics of women studied), according to the International Diabetes Federation (IDF) criteria [17]. VA/SA lower than 0.4 indicates that women did not suffer from visceral obesity. The individual and average values for waist circumference, triglycerides, HDL-cholesterol and systolic pressure exceeded the cut off points proposed by IDF (Table S1).
Circadian Clock Gene Expression
Data consistently revealed the presence of a circadian rhythm in CLOCK, BMAL1 and PER2 gene expression in both subcutaneous and visceral adipose tissue. In both depots the presence of rhythm was highly significant (P<0.001) (Table 1). Figure 1 graphically represents the circadian pattern of the clock genes studied in both subcutaneous and visceral adipose tissue depots. When relative gene expression among different 24 hours was analyzed by using repeated measures ANOVA test, statistical differences were found in subcutaneous (CLOCK: P = 0.012; PER2: P<0.001; BMAL1: P = 0.014) and in visceral ATs (CLOCK: P = 0.021; PER2: P<0.001; BMAL1: P = 0.001), evidencing timing differences in CLOCK, BMAL1 and PER2 expression.
In the graphs (Figure 2) the circles represent 24 hours and the radius corresponds to 10 units. The vector length is the amplitude of the rhythm and it points to its acrophase. In Figure 2 two relevant observations are noted, a) The presence of rhythmicity is clearly visible for all clock genes studied in both AT locations (2A: subcutaneous AT and 2B: visceral AT) taking into account that the ellipses of confidence did not include the center of graph and b) more importantly, PER2 expression (negative element) was in antiphase with respect to CLOCK (positive element) but in phase with BMAL1 (other representative gene of the positive limb of the clock) in the subcutaneous adipose tissue (Figure 2A). A situation that was not present in visceral adipose tissue where the acrophases of all studied genes were similar. Concretely PER2 acrophase in visceral AT was only 2 hours in advance of the acrophase of CLOCK and 1 hour in advance with respect to BMAL1 acrophase (Figure 2B).
Rhythmic expression of(1A),(1B) and(1C) in human subcutaneous (S) and visceral (V) adipose tissue (AT) (Control samples). CLOCK PER2 BMAL1 Adipose depots were isolated at 4-h intervals over the course of the day from adipose tissue cultures (time at ZT0 (1000 h), ZT4 (1400 h), ZT8 (1800 h), ZT12 (2200 h), ZT16 (0200 h) and ZT20 hours (0600 h)). Raw data (not mesor corrected) are represented by six black dots. Solid lines represent the estimated 24 h sinusoidal curve, in the population.,andexpression among different times of culture and statistical differences were analyzed in both depots (VAT and SAT) (repeated measures ANOVA test<0.05) evidences changes in gene expression due to time. Data of relative expression are represented as Arbitrary Units (AU). Data are reported as means ± S.E.M. CLOCK PER2 BMAL1 P
Polar (clock-like) representation of the estimates of the parameters of the rhythm forandin subcutaneous (2A) and visceral (2B) adipose tissue. CLOCK, PER2 BMAL1 In the graphs the circles represent 24 hours and the radius corresponds to 10 units. The vector length is the amplitude of the rhythm and it points to its acrophase. Dotted circles are the join 95% confidence limits for the vectors (if limits include the centre, the rhythm is not statistically significant), and dotted lines are the corresponding confidence interval for the acrophase. The population rhythms in control subcutaneous (S) and visceral (V) are clearly visible and statistically significant in both genes studied.
| 1A | CLOCK | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Control Subcutaneous Adipose Tissue | Control Visceral Adipose Tissue | |||||||||
| Population (T = 24 h) | Mesor (AU) | Amplitude (AU) | Acrophase (hh∶mm) | Percent Rhythm (%) | P | Mesor (AU) | Amplitude (AU) | Acrophase (hh∶mm) | Percent Rhythm (%) | P |
| Estimated | 1.4 | 0.36 | 00:12 | 75.54 | <0.001 | 1.78 | 0.73 | 08:55 | 76 | <0.001 |
| Lower limit | 1.27 | 0.27 | 23:13 | 1.48 | 0.55 | 07:57 | ||||
| Upper limit | 1.53 | 0.45 | 01:10 | 2.08 | 0.91 | 09:54 | ||||
Effect of dexamethasone exposure on circadian clock genes expression pattern
We observed a marked effect of dexamethasone (DEX) exposure (2 hours) on CLOCK, BMAL1 and PER2 circadian expression pattern with absence of circadian rhythms in both depots studied after DEX treatment for CLOCK (P>0.05) (Table 1) while for BMAL1 and PER2 this effect was only present for visceral AT (Table 1). The absence of rhythmicity in subcutaneous and visceral fat for CLOCK and in visceral AT for BMAL1 and PER2 after DEX treatment was also clearly visible in the polar representation (T = 24) in which the ellipses of confidence included the center of graph (Figure 3).
If using a sinusoid with a period of 12 hours for the population analysis (Figure 4), we observed that the clock genes expression rhythms were different when treated with DEX as compared with control (Figure 1). One important aspect is that for all the clock genes studied there was a change in the patterns of gene expression that was reflected in an adjustment to a sinusoidal curve of approximately 12 hours after DEX treatment. Indeed, we observed, in subcutaneous depot, immediately after the treatment with DEX that the expression of CLOCK decreased at ZT 4 (14:00 h) while it experienced a further increase after 8 hours reaching a peak at ZT 12 (22:00 h). A similar situation happened in visceral adipose tissue, with a significant decrease at ZT8 (18:00 h) and reaching its maximum at ZT 16 (02:00 h) (Figure 4). Similar results were observed for BMAL1 and PER2 (Figure 4). This change in the gene expression pattern is probably a result of the direct action of the dexamethasone that would produce a decrease in the expression of clock genes studied in the range of about 6 hours after the administration.
As in control samples, when we analyzed the relative gene expression among different times using repeated measures ANOVA test in DEX treated samples, statistical differences were found evidencing the rhythmicity of clock genes expression after treatment.
Polar (clock-like) representation of the estimates of the parameters of the rhythm forandin dexamethasone treated groups. CLOCK, PER2 BMAL1 In graphs 3A, 3B and 3C the circles represent 24 hours while in 3D, 3E and 3F it represents 12 hours, and the radius corresponds to 5 units. The vector length is the amplitude of the rhythm and it points to its acrophase. Dotted circles are the join 95% confidence limits for the vectors (if limits include the centre, the rhythm is not statistically significant), and dotted lines are the corresponding confidence interval for the acrophase. In 3A, 3B and 3C the absence of 24 hours rhythmicity is evident except for the subcutaneousandthat is statistically significant. In 3D, 3E and 3F the presence of an approximately 12 hours oscillation is evidenced in all treated groups. PER2 BMAL1
Effect of acute dexamethasone exposure on circadian expression of(1A),(1B) and(1C) in human subcutaneous (S) and visceral (V) adipose tissue (DEX samples). CLOCK PER2 BMAL1 Adipose depots were isolated at 4-h intervals over the course of the day from adipose tissue cultures (time at ZT0 (1000 h), ZT4 (1400 h), ZT8 (1800 h), ZT12 (2200 h), ZT16 (0200 h) and ZT20 hours (0600 h)). Raw data (not mesor corrected) are represented by six black dots. Solid and gray lines represent the fitted 12 h sinusoidal curve. Differences on the expression among different times of culture and statistical differences were analyzed in both depots (VAT and SAT) (repeated measures ANOVA test,<0.05) evidences changes in time. Data of relative expression are represented as Arbitrary Units (AU). Data are reported as means ± S.E.M. P
Discussion
The first objective of the present research was to characterize for the first time in human visceral and subcutaneous adipose tissue the rhythmicity of expression of CLOCK as compared with BMAL1 and PER2. In agreement with our hypothesis, we have demonstrated in humans the circadian rhythmicity of the CLOCK expression in both subcutaneous and visceral adipose tissue in culture conditions. This is consistent with previous observations for BMAL1, PER2 and other clock genes (CRY1) [3], cortisol-related genes [18] and some adipokines [19], [20] using similar experimental approaches. Moreover, in the present study the significant P-values obtained by periodic regression analysis in both adipose tissue depots show that CLOCK, BMAL1 and PER2 expression adjusts to a typical 24 h sinusoidal curve (see Table 1 and Figure 1). This fact is also clearly visible in the polar representation in which the ellipses of confidence did not include the center of graph (Figure 2).
Another relevant observation is the phase delay shown between the different adipose tissue locations for CLOCK. In fact, we observed that CLOCK in both adipose tissue depots, subcutaneous and visceral, oscillated in anti-phase. Thus acrophase in visceral adipose tissue was significantly delayed 8 h with respect to subcutaneous depot suggesting that the internal circadian regulation acts differently in both adipose tissues. Similar expression patterns have been observed for some glucocorticoids (GCs) metabolism-regulating genes, such as glucocorticoid receptor (GR) and 11β-hydroxysteroid dehydrogenase type 1 (11βHSD1) [18]. Although the molecular mechanisms underlying the distinct regulation of both peripheral adipose tissue depots by GCs remain currently largely unknown, our results are consistent with the notion that the effects of GCs on the gene networks that regulate many key functions in human adipose tissue differ between subcutaneous and visceral fats [21]. Moreover, adipose tissue glucocorticoid action relies on local enzymatic interconversion between 11βHSD1 and 11βHSD2 and glucocorticoid receptor (GR) availability, and both situations differ between subcutaneous and visceral fat [22]. On the other hand, corticoids secreted by the adrenal cortex could activate not only GR but also the mineralocorticoid receptor (MR) both of which are found in adipocytes. This activation could affect CLOCK circadian expression. Indeed, Tanaka et al. have demonstrated that aldosterone induces circadian gene expression of clock genes in H9c2 cardiomyoblasts and this mechanism is mediated through MR [23].
An interesting result found in the current work is that PER2 expression (negative element) was in antiphase with respect to CLOCK (positive element) in the subcutaneous adipose tissue. These data are in accordance with previous human studies performed confined to less invasive measurements in peripheral blood, oral mucosa and skin [24]–[26], and with studies of adipose tissue biopsies performed in both humans [27], [28] and animal models [29], showing an in vivo similar pattern of clock gene expression, exemplified by the anti-phase oscillation of negative and positive mRNAs. However in the current work we observed that BMAL1 (positive element) oscillated with approximately the same phase as PER2 (negative element). This unusual phase relationship has also been described in our previous study performed in vitro in human adipose tissue in culture conditions [3], and in other in vivo work in human peripheral blood mononuclear cells [30] and in mouse bone marrow [31]. In this sense it is important to remember that in addition to PER2, other genes are involved in the regulation of BMAL1 in the molecular circadian oscillator. Indeed, BMAL1 expression is under control of the “secondary clock loop” genes such as RORs, REV-ERBs and PPARα, which are linked to regulation of metabolism as well. Therefore, further investigations should determine if any change in the expression of these other components could be influencing the timing of BMAL1 expression. It could be also interesting to measure differences between (in vitro and in vivo) studies in a similar set of obese patients.
Differently to what happened in the subcutaneous adipose tissue, in the visceral region the acrophases of three genes studied were similar. Concretely PER2 acrophase was only 2 hours in advance of the acrophase of CLOCK and 1 hour in advance as compared to BMAL1 acrophase (Figure 2B). These findings are in agreement with a previous study where subcutaneous adipose tissue is classified as healthy adipose tissue [32], whereas that in the visceral AT, some disturbances occur in clock genes expression that could be related to the pathophysiology of this adipose region and its implications on the metabolic syndrome.
The second objective of our work was to investigate the possible effect of the glucocorticoid analogue DEX on both positive and negative clock genes expression in human adipose tissue in vitro. In this regard, our data revealed a marked effect of DEX exposure (2 hours) on CLOCK, BMAL1 and PER2 circadian expression patterns with absence of circadian rhythms in both depots studied after DEX treatment for CLOCK while for BMAL1 and PER2 this effect was only present for visceral fat. However, if using a sinusoid with a period of 12 hours for the population analysis, highly significant adjustments (P<0.01) were obtained in the two depots for the three genes studied. These altered patterns characterized by a loss of a typical 24 h sinusoidal curve adjustment is probably a result of the direct action of the dexamethasone that would produce a decrease in the expression of clock genes in the range of about 6 hours after the administration, which gives the plot a different aspect that would explain the adjustment to a sinusoidal curve of approximately 12 hours. It should be noted that the absence of the rhythm of 24 hours in visceral AT for the three genes studied and in subcutaneous AT only for CLOCK, may be due to the superposition of the effect produced by administration of DEX. Moreover, the time of administration of DEX could be relevant and action could probably depend on whether administration was performed close to the higher expression (achrophase) of the clock genes analyzed.
Of note, the overall effect of DEX seems to be to make the diurnal pattern in both adipose tissues temporally equivalent. Even so, when we analyzed clock gene expression among different times of culture using repeated measures ANOVA test, statistical differences were found in both depots treated with DEX, evidencing changes in CLOCK, BMAL1 and PER2 expression over the time. From these results we could hypothesize that GCs are particularly potent altering the circadian expression of both positive and negative clock genes in human adipose tissue. Interestingly, our current data in human adipose tissue are consistent with previous findings of Balsalobre et al., who have shown that a DEX shock transiently changes the phase of circadian gene expression in peripheral tissues of experimental animals [33]. Moreover, we have replicated this behavior which is consistent with the DEX induced CLOCK expression pattern previously described in bovine neutrophils [34]. The rhythmic secretion of GCs and their ability to phase shift peripheral clocks in adipose tissue, makes them valid candidates for signal establishing the link between the SCN pacemaker and the peripheral oscillators in adipose tissue [10].
One limitation of the current work was that all of the samples were from morbidly obese women. We must be cautious to extrapolate data to obese or normal weight subjects. In fact, the lack of a non-obese control group makes interpretation of the results more difficult, also regarding potential differences in glucocorticoid status between obese and non-obese individuals. However, to obtain enough AT sample from normal-weight individuals may be challenging and it could be also an ethical problem, considering the difficulties in obtaining enough fat from visceral and subcutaneous locations within the same patients to perform twelve different adipose tissue explants cultures (six for control and six for dexamethasone cultures).
In summary, 24 h patterns in CLOCK and BMAL1 (positive clock elements) and PER2 (negative element) mRNA levels were observed in human visceral and subcutaneous adipose tissue explants and these patterns were altered by an acute activation of glucocorticoid signalling making the diurnal pattern in both adipose tissues temporally equivalent. The time of administration of dexamethasone is important because action will depend on whether this administration is performed close to the higher expression (achrophase) of clock genes, but clearly dexamethasone treatment modified the rhythmicity pattern towards altered patterns with a period lower than 24 hours in all genes and in both tissues.