Endocannabinoid system dysfunction is observed in obesity, but the mechanisms by which this contributes to the etiology and the associated co-morbidities are not yet fully understood [14]. With discrepancies in the role of the CB₂ in obesity and adipose tissue function and inflammation, we aimed to investigate the effect of either chronic CB₂ agonism with AM1241 or chronic CB₂ antagonism with AM630 on inflammation, and adipose tissue in a DIO rat model. AM1241 or AM630 treatment of DIO rats fed an HFD diet failed to alter their body weight or food intake [6]. Surprisingly, both treatments reduced eWAT mass, while AM630 also reduced BAT weight, with a non-significant trend for AM1241 to reduce pWAT weights. The effects on reduced eWAT mass in DIO treated with either AM1241 or AM630 were associated with a decrease in plasma leptin concentrations, reduced leptin mRNA levels in BAT, and reduced leptin mRNA levels in eWAT (AM630 treatment only). Leptin, an adipokine, regulates whole-body energy balance through neuronal appetite pathways as well as a number of peripheral effects leading to decreased adipocyte fat storage [15]. In white adipocytes derived from obese patients, the leptin mRNA levels decreased following CB₂ stimulation with JWH-133 [16], whereas in CB₂-knockout mice following an HFD for a year, increased levels of leptin that correlated with adipose storage were displayed [12]. While we observed no changes in food intake with either AM1241 or AM630 levels, these combined results may implicate a protective role of leptin in conjunction with the CB₂ receptor that is independent of body weight/food intake. The effects of AM630 are more complicated, as the plasma concentrations of ghrelin and GLP-1 were also reduced at the same time.

In our DIO models, we observed differences in the effect of AM1241 on body weight/food intake between this study and JWH-015 in our previous study. There are several factors that could contribute to this discrepancy, including the following: (1) AM1241 is a partial agonist with respect to cAMP assays at the human CB₂ receptor, whereas, JWH-015 is a full agonist [5]; (2) receptor selectivity (AM1241 displays more CB₂/CB₁ binding selectivity compared to JWH-015) [17]; (3) species difference (while JWH-015 is a full agonist at cAMP assays at the human and mouse receptors, AM1241 is an inverse agonist at the mouse CB₂ receptor and a partial agonist at the human receptor [17]; and (4) the number and variety of off-target effects by both drugs [17]. All these factors may contribute to the differences observed in this study and our previous study.

There is widespread inflammation in obesity (including in animal models), but there is little information on whether CB₂ activation or inactivation can improve inflammation in obese rodents. CB₂ activation by either CB₂ selective agonists or CB₁/CB₂ agonists in the presence of CB₁ antagonists improves inflammation in a range of inflammatory models (as reviewed in [9]). In the current study, we have demonstrated that TNF-α mRNA expression was reduced in peri-renal WAT, which is in agreement with our previous observations that 21 days of treatment with JWH-015 reduces TNF-α in retroperitoneal WAT [5]. Similarly, 21 days of treatment with the CB₂ agonist JWH-133 in obese mice results in a decrease in the pro-inflammatory biomarkers TNF-α, IL-6, and IL-β [18]. Intriguingly, obese fat-fed ob/ob mice treated with CB₂ agonist JWH-133 for 15 days showed an increase in CB₂ expressions in the stromal vascular fraction of eWAT in correlation with increased adipose tissue inflammation [7]. However, following chronic activation of the CB₂ receptor with AM1241 in the current study, we did not observe any alterations in a wide range of plasma cytokines, or the expression of IL-6 in any of the adipose tissue depots investigated, or TNF-α in any of the other adipose tissue depots. Overall, this suggests that CB₂ agonism does not improve obesity-driven inflammation. Chronic treatment with the CB₂ antagonist AM630 also reduced TNF-α mRNA levels in pWAT and increased IL-6 mRNA levels in BAT. These alterations did not result in changes in any inflammatory plasma concentration measured. This is in contrast to a previous study that showed that AM630 reduced fat inflammation [7]. This discrepancy may be due to differences in the dose used (1 mg/kg/day for 15 days) or the fact that those experiments were performed in ob/ob mice (note that AM630 had no effect in the lean ob+/ob mice, further supporting a link between leptin and CB₂ receptors). It should be noted that while there is evidence that CB₂ is expressed in the stromal vascular fraction of WAT and not in mature adipocytes themselves [7], an HFD increases CB₂ expression in eWAT. In our study, AM630 decreased CB₂ mRNA levels in eWAT and pWAT (with a trend for AM1241 to do the same in eWAT). We measured mRNA in tissue depots, and it may be worthwhile in the future to examine changes in mRNA levels in the SVF instead, where the CB₂ receptor is expressed.

We observed a decrease in the epididymal fat pad as a percentage of body weight following AM1241 treatment. A direct correlation between low leptin levels and a decrease in the epididymal fat pad mass has been previously observed in rats [19]. In mice, epididymal fat has been found to initiate leptin control via afferent nerve signaling to control appetite. The increased expression of UCP1 in epididymal fat reduced appetite via afferent nerve signaling [20]. Our results found that CB₂ activation and inhibition reduced epidydimal fat expression of UCP1, which is consistent with the lack of effect on appetite that we observed [6]. The reduction in the epididymal fat pad mass and the low circulating concentrations of leptin detected imply that our results further depict a protective role of leptin working in conjunction with CB₂ independent of affecting body weight and food consumption. In agreement with this, our results found that both the activation and inhibition of CB₂ reduced the expression of UCP1 in epididymal adipose, without any changes in food intake. BAT is an important organ for controlling whole-body energy homeostasis through its roles in thermoregulation and glucose uptake [21]. While there is some evidence that CB₁ antagonism may be beneficial for increased the BAT activity in rodents and humans [22], there is little research on CB₂ and its impact on BAT function. For example, UCP1 mRNA in BAT in CB₂-knockout mice is unaltered [12] and JWH-015-treated HFD mice show no changes in the UCP1 protein [5]. Cnr1 and Cnr2 mRNAs were not detected in BAT; hence, the effects of AM630 and AM1241 on the transcriptional changes in BAT are most likely due to a secondary indirect effect [23]. Since BAT is highly innervated, this could be due to alterations in the sympathetic tone to BAT. Another possible mechanism is the reduction in circulating leptin levels following both AM630 and AM1241 treatment. Leptin administration to rats increases BAT UCP1 mRNA levels, which are dependent upon the sympathetic activation of BAT [23]. While we show that neither the CB₁ nor CB₂ receptors were detected in BAT, the treatment of DIO rats with AM1241 reduces UCP1, Adrb3, Slc2a4, and PRDM16 mRNA without affecting the BAT mass.

UCP1 is a mitochondrial protein that is responsible for non-shivering thermogenesis and can be activated by the neurotransmitter noradrenaline, which acts at BAT β₃-ARs to increase thermogenesis [21]. The reduced expression of both Adrb3 and UCP1, and the transcriptional co-regulator PRDM16, which controls the development of brown adipocytes in BAT, may suggest a blunting of thermogenic responses in these animals. Adrb3 is a regulator of CB₂ thermogenesis in BAT through the upregulation of UCP1 [24]. This action is potentiated by PRDM16, which may be a cross-talk regulator of BAT thermogenesis and glucose clearance in other tissues [25]. BAT is an important glucose-clearing organ, and a decreased expression of Slc2a4 (GLUT4) may suggest impaired glucose clearing by BAT. Chronic treatment of DIO rats with AM630 also reduced UCP1 and Slc2a4 mRNA levels and resulted in a decrease in BAT mass.

Browning of WAT has been proposed as a mechanism to combat obesity and its co-morbidities [26], and browning is typically defined as an increase in the UCP1 mRNA/protein or an increase in other brown adipocyte genes, such as CPT1b and PDRM16. While the CB₂ agonist JWH-133 increases the UCP1 protein in lean patient-derived white adipocytes, this effect is severely blunted in obese patient-derived white adipocytes [27]. In CB₂-knockout mice fed an HFD, there is no evidence of browning of eWAT, as defined by a lack of changes in UCP1, Cox8b, or Cidea mRNA levels [8]. In our study, we observed genes involved in thermogenesis with decreased CPT1b mRNA in pWAT and Adrb3 and PRDM16 mRNA in eWAT following treatment with AM1241, while AM630 treatment decreased Adrb3 and PRDM16 mRNA levels in eWAT.

Interestingly, the heart weighed more in the AM630 and AM1241 treatment groups compared with vehicle-treated DIO rats; however, when expressed as a percentage of the total body weight, only with the CB₂ agonist AM1241 did we observe a significant increase in the heart weight (grams). This result reinforces the notion that increasing CB₂ may have a cardiac effect rather than a metabolic influence on these animals. Although we did not test the impact of CB₂ agonist treatment on the cardiac tissue function, we have previously reported that these animals experienced a reduced systolic BP, urinary protein, urinary albumin, urinary sodium excretion, and renal fibrotic markers [6]. Therefore, the agonism of CB₂ appears to be having a positive renal-cardiac effect, which is supported by the increase in the heart size. CB₂ receptor agonist exposure in the heart has been found to protect the heart from ischemic damage in rats [28]. However, an enlarged heart can be a result of cardiomegaly, explaining the increased organ weight [29]. CB₂ has been identified as having an anti-inflammatory effect during cardiac tissue remodeling [30]. This would be anticipated given the role of CB₂ in cardiac repair, and we would have seen an increase in systemic cytokines if this were the case; however, no change was detected despite the increase in heart weight. Moreover, there is a need to determine macrophage infiltration (M1 and M2 markers) at variable time points in adipose tissues to determine if there are direct effects of modulating CB₂ on inflammation. Given the close association between obesity and cardiovascular disease risk, further investigation of the effects of CB₂ activation on the cardiac muscle is warranted. Despite the lack of effects, such as weight loss and changes in food intake, we demonstrated a yet-to-be-elucidated role in CB₂ modulation in altering plasma leptin levels and marker of thermogenesis. However, this study had a number of limitations, namely, the dose and duration of treatment. At the time of the study design, few investigations into CB₂ modulation effects had been conducted in DIO animal models, with no studies focusing on rodents; therefore, the concentrations of AM630 [31] and AM1241 [32] were based on non-obese models.

While further dose–response studies are warranted, the doses used here are similar to those used in other studies using AM630 [33] and AM1241 [34]. We hypothesized a link between CB₂ modulation and cardiac-renal effects; while we present evidence of this at an in vivo level, we did not look at cellular adaptations in cardiac tissue. Similarly, the reduction in circulating leptin in plasma that occurred with 6 weeks of both CB₂ agonism and antagonist looking at changes in central leptin signaling would be beneficial.

Overall, CB₂ modulation in DIO had little effect on inflammatory markers in the plasma and in adipose tissue. However, CB₂ modulation reduced the circulating leptin levels in both the CB₂ agonist and antagonist treatment groups. Moreover, CB₂ modulation altered specific adipocyte genes involved in thermogenic pathways. Collectively, our results show that CB₂ modulation plays a role in decreasing circulating leptin levels and modulating thermogenic mRNA in adipose tissue.