Volume 173, Issue 12 p. 1899-1910

REVIEW ARTICLE

Free Access

An update on PPAR activation by cannabinoids

Corresponding Author

Saoirse Elizabeth O'Sullivan

School of Medicine, Royal Derby Hospital, University of Nottingham

Correspondence Saoirse Elizabeth O'Sullivan, School of Medicine, Royal Derby Hospital, University of Nottingham, Nottingham, DE22 3DT, UK. E-mail: [email protected]Search for more papers by this author

Saoirse Elizabeth O'Sullivan,

Corresponding Author

Saoirse Elizabeth O'Sullivan

School of Medicine, Royal Derby Hospital, University of Nottingham

First published: 14 April 2016

https://doi.org/10.1111/bph.13497

Citations: 343

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Abstract

Some cannabinoids activate the different isoforms of PPARs (α, β and γ), as shown through the use of reporter gene assays, binding studies, selective antagonists and knockout studies. Activation of all isoforms, but primarily PPARα and γ, mediates some (but not all) of the analgesic, neuroprotective, neuronal function modulation, anti-inflammatory, metabolic, anti-tumour, gastrointestinal and cardiovascular effects of some cannabinoids, often in conjunction with activation of the more traditional target sites of action such as the cannabinoid CB₁ and CB₂ receptors and the TRPV1 ion channel. PPARs also mediate some of the effects of inhibitors of endocannabinoid degradation or transport. Cannabinoids may be chaperoned to the PPARs by fatty acid binding proteins. The aims of this review are to update the evidence supporting PPAR activation by cannabinoids and to review the physiological responses to cannabinoids that are mediated, and not mediated, by PPAR activation.

Abbreviations

2-AG: 2-arachidonoyl-glycerol
AJA: ajulemic acid
CBD: cannabidiol
FAAH: fatty acid amide hydrolase
FABP: fatty acid binding protein
OEA: oleoylethanolamide
PEA: palmitoylethanolamide
THC: Δ⁹-tetrahydrocannabinol
VCAM: vascular cell adhesion molecule

Tables of Links

TARGETS
GPCRs^a
CB₁ receptor
CB₂ receptor
GPR55
Nuclear hormone receptors^b
PPARα
PPARγ
Other proteins^c
FABP5, fatty acid binding protein 5
Enzymes^d
COX2
FAAH, fatty acid amide hydrolase

LIGANDS
15d-PGJ2, 15-deoxy-Δ^l2,14-PGJ₂	JWH015
2-AG, 2-arachidonoyl-glycerol	Methanandamide
Anandamide	OEA, oleoylethanolamide
Arachidonyl-2′-chloroethylamide	Oleamide
NADA, N-arachidonoyl-dopamine	PEA, palmitoylethanolamide
CBD, cannabidiol	THC, Δ⁹-tetrahydrocannabinol
CP55940	URB597
ICAM	VCAM, vascular cell adhesion molecule
IL-2	Virodhamine
IL-8, CXCL8	WIN55,212-2

These Tables list key protein targets and ligands in this article which are hyperlinked to corresponding entries in http://www.guidetopharmacology.org, the common portal for data from the IUPHAR/BPS Guide to PHARMACOLOGY (Pawson et al., 2014) and are permanently archived in the Concise Guide to PHARMACOLOGY 2015/16 (^a,b,c,dAlexander et al., 2015a,b,c,d).

Introduction

The PPARs are a family of nuclear hormone receptors with three isoforms (α, δ and γ, Alexander et al., 2015b). PPARs form heterodimers with the retinoid X receptor and bind to DNA sequences called PPAR response elements, leading to changes in the transcription of target genes. Ligand binding to PPARs is associated with a change in the variety of regulator proteins that bind to a third site on PPARs, and these are thought to modulate transactivation. The target genes of PPARs are involved in the regulation of metabolism and energy homeostasis, cell differentiation and inflammation (see Friedland et al., 2012; Menendez-Gutierrez et al., 2012; Neher et al., 2012; Poulsen et al., 2012, for reviews).

PPARs have large ligand binding domains and can be activated by a number of ligands of different chemical structure, including a number of plant extracts (Wang et al., 2014). Endogenous activators of PPARs include the unsaturated fatty acids linolenic acid, linoleic acid, petroselenic acid and arachidonic acid, with EC₅₀ values in the 2–20 μM range (Kliewer et al., 1997). Eicosanoids such as 15-deoxy-Δ^l2,14-PGJ₂ (15d-PGJ₂) and 8S-HETE also interact with PPARs, with pEC₅₀ values of about 6.3 (Kliewer et al., 1997). Clinically, PPARα agonists are used in the treatment of cholesterol disorders and for their effects on triglyceride metabolism (fibrate drugs, Katsiki et al., 2013), and PPARγ agonists are used in the treatment of insulin resistance and decrease blood glucose levels (thiazolidinediones; Cariou et al., 2012).

Since 2002, evidence has accumulated that endocannabinoids, endocannabinoid-like compounds, phytocannabinoids and synthetic cannabinoid ligands bind to and activate PPARs (O'Sullivan, 2007; O'Sullivan, 2013). This link has been identified through reporter gene assays, binding studies, the use of selective antagonists, knockout animals and siRNA knockdown studies, and these data are summarized in Tables 1 and 2. Because of this, investigators are increasingly assessing potential roles for PPAR activation as the basis of the physiological effects of cannabinoids. This means that a clearer picture of the relevance of PPAR activation by some cannabinoids is now emerging. The aims of this review are to update the evidence for cannabinoids as agonists of PPARs and to review the effects of cannabinoids that might be mediated through PPARs. I will also review the effects of cannabinoids that have been shown to be PPAR independent.

Table 1. Current evidence for cannabinoid activation of PPARα

	Binding studies	Transcriptional activity	Blockade by selective antagonists	Use of knockouts/siRNA
Phytocannabinoids and their derivatives
THC	a	Takeda et al., 2014	Fishbein-Kaminietsky et al., 2014	–
CBD	–	–	–	–
AJA	a	a	–	–
Endocannabinoids and endocannabinoid-like compounds
AEA	Sun et al., 2007	Sun et al., 2007	Romano and Lograno, 2012	–
2-AG	–	Kozak et al., 2002	–	–
Endocannabinoid-like compounds
OEA	Fu et al., 2003; Sun et al., 2007	Fu et al., 2003; Sun et al., 2007; Kaczocha et al., 2012	Melis et al., 2008; Zhou et al., 2012; Hind et al., 2015	Fu et al., 2003; Guzman et al., 2004; Sun et al., 2007; Campolongo et al., 2009; Gaetani et al., 2010; Bilbao et al., 2013
PEA	–	LoVerme et al., 2005	Melis et al., 2008; Koch et al., 2011; Scuderi et al., 2011, 2012; De Novellis et al., 2012; Khasabova et al., 2012; Kumar et al., 2012; Romano and Lograno, 2012; Ambrosino et al., 2013; Citraro et al., 2013; Esposito et al., 2014; Borrelli et al., 2015; Hind et al., 2015	LoVerme et al., 2005, 2006; D'Agostino et al., 2012; Di Paola et al., 2012; Kumar et al., 2012; Sasso et al., 2012; Di Cesare Mannelli et al., 2013; Paterniti et al., 2013
Noladin ether	Sun et al., 2007	Sun et al., 2007	–	–
Virodhamine	Sun et al., 2007	Sun et al., 2007	–	–
Oleamide	Dionisi et al., 2012	Dionisi et al., 2012	–	–
Synthetic compounds
WIN55,212-2	Sun et al., 2007	Sun et al., 2007	Downer et al., 2012	–
ACEA			Palomba et al., 2015

^a Sun et al. (2007 found THC did not bind to PPARα; Liu et al. (2003) showed that AJA does not bind to or activate PPARα.
–, no known data; ACEA, arachidonyl-2′-chloroethylamide; AEA, anandamide.

Table 2. Current evidence for cannabinoid activation of PPARγ

	Binding studies	Transcriptional activity	Blockade by selective antagonists	Use of siRNA
Phytocannabinoids and their derivatives
THC	Granja et al., 2012	O'Sullivan et al., 2005	O'Sullivan et al., 2006, 2005; Carroll et al., 2012; Vara et al., 2013	Vara et al., 2013
THCV		a
CBD	O'Sullivan et al., 2009a; Granja et al., 2012	O'Sullivan et al., 2009a; Hegde, 2015	O'Sullivan et al., 2009a; Esposito et al., 2011; De Filippis et al., 2011; Ramer et al., 2013; Scuderi et al., 2014a; Hegde et al., 2015; Hind et al., 2016	Ramer et al., 2013
AbnCBD			Bosier et al., 2013
AJA	Liu et al., 2003; Ambrosio et al., 2007	Liu et al., 2003	Gonzalez et al., 2012	–
CBG	Granja et al., 2012	Granja et al., 2012	–	–
CBC	Granja et al., 2012	–	–
Cannabigerol quinone	Granja et al., 2012	Granja et al., 2012	–	–
Endocannabinoids
AEA	Bouaboula et al., 2005	Bouaboula et al., 2005; Ahn et al., 2015	Rockwell and Kaminski, 2004; Bouaboula et al., 2005; O'Sullivan et al., 2009b	–
2-AG	–	Rockwell et al., 2006; Zhang et al., 2014a	Rockwell et al., 2006; Du et al., 2011; Zhang et al., 2014	–
Endocannabinoid-like compounds
NADA	–	O'Sullivan et al., 2006a	O'Sullivan et al., 2009b	–
OEA	–	a	–	–
PEA	–	O'Sullivan et al., 2006a	Costa et al., 2008	–
Oleamide	Dionisi et al., 2012	Dionisi et al., 2012	–	–
Synthetic compounds
Methanandamide	–	–	Eichele et al., 2009	–
WIN55,212-2	–	O'Sullivan et al., 2006; Fakhfouri et al., 2012	Giuliano et al., 2009; Mestre et al., 2009; Fakhfouri et al., 2012; Hong et al., 2013; Payandemehr et al., 2015	–
CP55,940	–	O'Sullivan et al., 2006	–	–
HU331	Granja et al., 2012	–	–	–
JWH015	a	–	Vara et al., 2013	Vara et al., 2013

aTHCV (O'Sullivan et al. 2006); 2-AG (Kozak et al. 2002; Ahn et al. 2015), PEA (LoVerme et al., 2005) or NADA (Ahn et al. (2015 did not increase transcriptional activity of PPARγ; OEA did not bind to or activate PPARγ (Fu et al., 2003); JWH015 did not bind to PPARγ (Vara et al., 2013).
–, no known data; THCV, tetrahydrocannabivarin; AbnCBD, abnormal CBD; CBG, cannabigerol; CBC, cannabichrome; AEA, anandamide; NADA, N-arachidonoyl-dopamine.

Evidence of PPAR activation by cannabinoids

A summary of the current data supporting the activation of PPAR nuclear receptors by some cannabinoid compounds and their derivatives is provided in Table 1 for PPARα and Table 2 for PPARγ. These Tables do not include those studies where a role for endocannabinoid activation of PPARs has been proposed after administration of fatty acid amide hydrolase (FAAH) inhibitors (Jhaveri et al., 2008; Sagar et al., 2008; Mazzola et al., 2009; Luchicchi et al., 2010; Khasabova et al., 2012; Sasso et al., 2013; Justinova et al., 2015; Rock et al., 2015), monoacylglycerol lipase inhibitors (Zhang et al., 2014), N-acylethanolamine acid amidase inhibitors (Khasabova et al., 2012; Sasso et al., 2013), endocannabinoid uptake inhibitors (Roche et al., 2008; Loria et al., 2010; Reyes-Cabello et al., 2012) or fatty acid binding proteins (FABP) inhibitors (Kaczocha et al., 2014), and where the activating ligand was not specifically identified, but a role for PPAR activation was implied when endocannabinoid tone was increased.

Phytocannabinoids and their derivatives

Phytocannabinoids and their derivatives including Δ⁹-tetrahydrocannabinol (THC), cannabidiol (CBD), abnormal CBD, cannabigerol, cannabigerol quinine, cannabichrome and ajulemic acid (a synthetic analogue of a tetrahydrocannabinol metabolite, AJA) can all bind to, increase the transcriptional activity of and exert effects that are inhibited by selective antagonists of PPARγ (see Table 2 for references), suggesting that this is a property of many phytocannabinoid compounds. However, tetrahydrocannabivarin does not increase the transcriptional activity of PPARγ (O'Sullivan et al., 2006). By contrast, there are less data on the effects of phytocannabinoids at PPARα. Sun et al. (2007 found that THC does not bind to PPARα, but Takeda et al. (2014) recently showed that THC did increase the transcriptional activity of PPARα. AJA also does not bind to PPARα or δ (Liu et al., 2003).

Endocannabinoids and their derivatives

Strong evidence now exists that the endocannabinoid-like compounds oleoylethanolamide (OEA) and palmitoylethanolamide (PEA) activate PPARα, as shown through binding studies, reporter gene assays, the use of antagonists and also the absence of responses to these compounds in PPARα knockout mice (see Table 1 for references). Anandamide, 2-arachidonoyl-glycerol (2-AG), noladin ether, virodhamine and oleamide have also been shown to activate PPARα, although there is less evidence for this (Table 1). Several studies have shown that anandamide and 2-AG also activate PPARγ (Table 1), and although less investigated, there is evidence that N-arachidonoyl-dopamine, PEA and oleamide also activate PPARγ, although studies are contradictory in this area. In addition, studies have shown that some of the metabolites of endocannabinoid degradation are PPAR activators. Raman et al. (2011) showed that 2-AG-derived 15d-PGJ₂-glycerol ester activates PPARγ in a reporter gene assay, and Kozak et al. (2002) showed that 2-AG-derived 15-hydroxyeicosatetraenoic acid glyceryl ester increases the transcriptional activity of PPARα. Arachidonic acid derived from anandamide also activates PPARδ (Yu et al., 2014). Fu et al. (2003) also showed that OEA activates the transcriptional activity of PPARδ, Dionisi et al. (2012) showed that oleamide increases the transcriptional activity of and binds to PPARδ, Paterniti et al. (2013) showed that the neuroprotective and anti-inflammatory effects of PEA were inhibited by a PPARδ antagonist, and an indirect activation of PPARδ by anandamide (being degraded into arachidonic acid) is speculated to play a role in regulating cognitive function (Yu et al., 2014). However, 2-AG metabolites (Kozak et al., 2002) and PEA (LoVerme et al., 2005) do not activate PPARδ. Together, this suggests that activation of PPARs by endocannabinoids, endocannabinoid-like molecules and some of their metabolites is a common feature of these compounds.

Synthetic cannabinoids

Fewer studies have investigated the potential for synthetic cannabinoid compounds to activate PPARs. WIN55,212-2 binds to and activates the transcriptional activity of PPARα and PPARγ (Tables 1 and 2), and arachidonyl-2′-chloroethylamide, CP55940, HU331 and JWH015 activate PPARγ (Table 2).

Cannabinoids, fatty acid binding proteins (FABPs) and PPARs

In the 2007 review, I speculated on the potential mechanisms of cannabinoid/PPAR interactions, suggesting that cannabinoids could bind directly to PPARs and be converted into PPAR-active metabolites or that activation of cell surface cannabinoid receptors initiates intracellular signalling cascades that lead to the activation of PPARs indirectly. Another possibility that has recently come to light is that cannabinoids may be actively transported to the nucleus and PPARs by FABPs. FABPs are intracellular lipid binding proteins, and binding to FABPs by ligands promotes nuclear localisation and interaction with PPARα (Hughes et al., 2015). Kaczocha et al. first showed in 2009 that anandamide was transported by FABP5 and 7 from the plasma membrane to FAAH for hydrolysis (Kaczocha et al., 2009). They later showed that OEA is transported to the nucleus and to PPARα by FABP5 and that FABP inhibition reduced the ability of OEA to activate PPARα (Kaczocha et al., 2012). THC and CBD were also recently shown to be transported intracellularly by FABPs (Elmes et al., 2015), which may be the mechanism for their delivery to the nucleus for PPAR activation. Together, this suggests that FABPs can direct cannabinoids to enzymes for degradation or to the nucleus for PPAR activation. It is not yet clear what might be driving one pathway over another. FABP5 has also been shown to promote the cellular uptake and hydrolysis of anandamide, and that the metabolites derived from this are PPARδ activators (Yu et al., 2014), so activation of PPARs is still achieved despite anandamide degradation. On the other hand, inhibition of FABPs reduces inflammatory pain in mice, and this can be inhibited by CB₁ receptor or PPARα antagonists (Kaczocha et al., 2014), suggesting here that the FABP-direct degradation of endocannabinoids can also limit their ability to activate PPARα.

Physiological responses to cannabinoids mediated by PPARs

From the first indication that cannabinoids activate PPARs, an important task has been to establish which of the physiological effects of cannabinoids might be mediated, at least in part, through activation of these receptors. This is particularly important to establish because the affinity of cannabinoids for PPARs tends to be in the micromolar range (although this is not dissimilar to the affinity of other endogenous ligands for PPARs, Kliewer et al., 1997). Fortunately, many studies have now include tools to assess a role for PPAR activation (see Table 1 and 2 for references). Below is a summary of the evidence for PPAR activation as a mechanism of action (often in combination with some of the more traditional cannabinoid targets) for cannabinoids in some of the commonly recognized physiological effects of cannabinoids.

Neuroprotection

In terms of stroke models, a role for PPARα and γ activation has been postulated in the actions of several cannabinoids. OEA reduces infarct volume after cerebral artery occlusion in mice, which is absent in PPARα knockout mice (Sun et al., 2007). Similarly, Zhou et al. (2012 showed that OEA improves neurological dysfunction and reduces infarct size and brain oedema after cerebral artery occlusion, which was inhibited by PPARα antagonism. In an in vitro model of the blood–brain barrier (BBB), OEA increases monolayer resistance (i.e. reduces permeability) via PPARα activation, and both OEA and PEA are able to reduce the hyperpermeability response to oxygen–glucose deprivation, sensitive to PPARα antagonism (Hind et al., 2015). In the same model, CBD is protective against increased permeability of the BBB associated with oxygen–glucose deprivation; however, in this case, the effects of CBD were sensitive to PPARγ antagonism (Hind et al., 2016).

In models of Alzheimer's disease, PEA blunts the expression of pro-inflammatory molecules in astrocytes in response to β-amyloid in a PPARα-dependent, PPARγ-independent manner (Scuderi et al., 2011), and PEA decreases infiltrating astrocytes in hippocampal slices treated with β-amyloid, sensitive to PPARα, but not PPARγ, antagonism (Scuderi et al., 2012). Chronic PEA administration also protects against the memory deficits induced by β-amyloid, which was absent in PPARα-null mice (D'Agostino et al., 2012). PEA protects against excitotoxicity in hippocampal cultures, which is blocked by a PPARα but not PPARγ antagonist (Koch et al., 2011), and may be a mechanism by which PEA is protective in neurodegenerative disorders. This effect is not unique to PEA; 2-AG also inhibits β-amyloid formation by inhibiting the β-site amyloid precursor protein-cleaving enzyme, which was inhibited after PPARγ knockdown (Zhang et al., 2014). This study showed that inhibition of the degradation of 2-AG reduced inflammation and improved cognitive function in a mouse model of Alzheimer's disease, which was inhibited by a PPARγ antagonist. CBD also protects against β-amyloid neurotoxicity and inflammation in rats, reduced by PPARγ antagonism (Esposito et al., 2011). In human neuronal cells, CBD reduces β-amyloid expression and increases amyloid precursor protein (APP) ubiquitination, which was inhibited by PPARγ antagonism (Scuderi et al., 2014a). In vivo, WIN55,212-2 reduces β-amyloid-induced neuroinflammation and improved memory function in rats, which was inhibited by antagonists of CB₁ and CB₂ receptors and PPARγ (Fakhfouri et al., 2012). Together, this suggests that activation of both PPARα and PPARγ by a range of cannabinoids is protective in models of Alzheimer's disease.

In a model of multiple sclerosis, increasing local levels of endocannabinoids by inhibiting their uptake (using UCM707) had neuroprotective effects against excitotoxicity, which could be inhibited by CB₁ and CB₂ receptor and PPARγ antagonism (Loria et al., 2010). In another animal model of inflammatory-demyelinating disease, the protective effects of WIN55,212-2 were inhibited by a PPARα antagonist (Downer et al., 2012). In this study, it was identified that WIN55,212-2, through PPARα, activates the IFN-β promoter, which exerts a wide range of positive effects.

In models of epilepsy, anandamide and PEA decrease epileptic spike–wave discharge, which were inhibited by CB₁ receptor antagonism (both) and PPARα antagonism (PEA only) (Citraro et al., 2013). WIN55,212-2 has anti-convulsant effects on GABA antagonist-induced seizures that are inhibited by CB₁ receptor, PPARα and γ antagonists (Payandemehr et al., 2015). THC has neuroprotective effects in a cell culture model of Parkinson's disease that was not inhibited by CB₁ receptor blockade, but was inhibited by a PPARγ antagonist (Carroll et al., 2012). PPARγ activation after FAAH inhibition with URB597 also contributes to the anti-dyskinetic effects after chronic levodopa administration (Martinez et al., 2015).

Reward

Up-regulation of local endocannabinoids by FAAH inhibition, or administration of OEA and PEA, inhibits neuronal responses in the reward area of the brain to nicotine but not cocaine or morphine (Luchicchi et al., 2010), which was sensitive to both CB₁ receptor and PPARα antagonism (Melis et al., 2008; Luchicchi et al., 2010). Nicotine reward was also reduced by FAAH inhibition in primates and the effect of FAAH inhibition was reversed by PPARα antagonism (Justinova et al., 2015), suggesting that FAAH inhibitors might be useful smoking cessation tools. A similar effect on nicotine reward mediated by PPARα was seen in response to methyl OEA, a long-lasting form of OEA, or to PPARα agonists (Mascia et al., 2011).

Memory and cognition

Mazzola et al. (2009) showed that memory acquisition in rats is enhanced by the FAAH inhibitor URB597, which was sensitive to PPARα antagonism. Campolongo et al. (2009) showed that OEA administration also has a memory-enhancing effect that was absent in PPARα-null mice. In Alzheimer's disease models, PEA protects against memory deficits, which was absent in PPARα-null mice (D'Agostino et al., 2012), and WIN55,212-2 improves memory function, which was inhibited by a PPARγ antagonist (Fakhfouri et al., 2012). Low doses of THC (administered either before or after the insult) also protect against the cognitive damage (object recognition) induced by inflammation, and this effect was inhibited by a CB₁ receptor or PPARγ antagonist (but not by CB₂ receptor antagonism) (Fishbein-Kaminietsky et al., 2014).

Analgesia

Several studies have shown that PEA has analgesic effects in vivo in several models of pain behaviour that are inhibited by PPARα antagonists or are absent in PPARα knockout mice (LoVerme et al., 2005; de Novellis et al., 2012; Sasso et al., 2012; Di Cesare Mannelli et al., 2013). The PPARα-mediated analgesic effects of PEA have also been demonstrated in peripheral sensory nerve cells, which additionally involved the activation of TRPV1 channels, but not CB₁ or CB₂ receptors (Ambrosino et al., 2013). A PEA analogue, palmitoylallylamide, also reduces hypersensitivity in neuropathic pain that was inhibited by antagonists of CB₁ and CB₂ receptors and of PPARα (Wallace et al., 2007). By contrast, Costa et al. (2008) found that the analgesic effects of PEA in neuropathic pain involved CB₁ receptors, TRPV1 channels and PPARγ, but not PPARα or CB₂ receptors.

Up-regulation of local endocannabinoid levels by inhibition of FAAH with URB597 induces analgesia in an inflammatory pain model, and this was inhibited by a PPARα antagonist but not a CB₁ receptor antagonist (Sagar et al., 2008) or a PPARγ antagonist (Jhaveri et al., 2008). In the Jhaveri study, URB597 increased local levels of anandamide and 2-AG, so either ligand could be activating PPARα. Interestingly, Jhaveri et al. (2008) also showed that COX2 inhibition increased local PEA levels and caused analgesia that was inhibited by a PPARα antagonist. Another FAAH inhibitor, ST4070, also reduces neuropathy, increases anandamide and 2-AG levels and is sensitive to antagonists of CB₁, receptors, TRPV1 channels and PPARα antagonism (Caprioli et al., 2012). A similar effect was seen with an inhibitor of N-acylethanolamine acid amidase (ARN077), which was found to have anti-nociceptive effects in rodent models that were inhibited by a PPARα antagonist (but not CB₁ or CB₂ receptor antagonists) and absent in PPARα knockout mice, associated with an increase in OEA and PEA levels (Khasabova et al., 2012; Sasso et al., 2013). It has also been shown that inhibition of FABPs reduces inflammatory pain in mice, and this effect was inhibited by antagonists of CB₁ receptors or PPARα, which was associated with an up-regulation of anandamide (but not 2-AG, OEA or PEA), and anandamide was suggested as the activating ligand (Kaczocha et al., 2014).

Anti-tumour effects of cannabinoids

In many cancer cell lines, there is much evidence now to show that cannabinoids induce apoptosis via PPARγ. This has been shown for WIN55,212-2 in liver cancer cells (Giuliano et al., 2009; Hong et al., 2013), for methanandamide in cervical carcinoma cells and lung carcinoma cells (Eichele et al., 2009), for CBD in human lung cancer cells (Ramer et al., 2013) and for THC and JWH015 (a CB₂ receptor agonist) in liver cancer cells (Vara et al., 2013). The anti-tumour effect of THC in human breast cancer cells involved the activation of both PPARα and γ (Takeda et al., 2013, 2014). Collectively, this suggests that PPAR activation is involved in the anti-tumour effects of cannabinoids. In support of this, there is increasing evidence that the thiazolidinedione class of PPARγ ligands, normally used in the treatment of diabetes, may have a potential new role in the treatment of cancer (Joshi et al., 2014).

Cardiovascular system

THC causes time-dependent, PPARγ-dependent vasorelaxation in rat isolated arteries (the aorta and superior mesenteric artery) that is dependent on production of NO and hydrogen peroxide and on superoxide dismutase activity (O'Sullivan et al., 2005). THC also enhances vasodilator responses in isolated arteries, which could be inhibited by a PPARγ antagonist (O'Sullivan et al., 2006). A similar time-dependent and PPARγ-sensitive vasorelaxant response in the rat aorta was also observed in response to CBD (O'Sullivan et al., 2009a) and the endocannabinoids anandamide and N-arachidonoyl dopamine, but not PEA (O'Sullivan et al., 2009b). Romano & Lograno (2012) also showed a time-dependent vasorelaxant response to anandamide and PEA in the bovine ophthalmic artery, but this effect was inhibited by a PPARα, but not a PPARγ, antagonist. Kumar et al. (2012) showed that PEA increases aqueous humour outflow in porcine eyes, which is inhibited by PPARα antagonism or knockdown.

In a model of multiple sclerosis, WIN55,212-2 suppresses the increased intercellular adhesion molecule and vascular cell adhesion molecule (VCAM) in brain endothelium, sensitive to PPARγ, but not CB₁ or CB₂ receptor antagonists (Mestre et al., 2009). CBD also reduces VCAM in human brain microvascular endothelial cells via PPARγ (Hind et al., 2016). An analogue of OEA, (Z)-(S)-9-octadecenamide, N-(2-hydroxyethyl, 1-methyl), decreases the expression of VCAM and ICAM and monocyte adhesion in response to inflammation in HUVECs, which was antagonized by PPARα (Chen et al., 2011). A reduction in these markers of endothelial activation may be a result of the anti-inflammatory effects of PPAR activation.

Suppression of PPARα is postulated to mediate the cardioprotective effects of WIN55,212-2 in doxorubicin-induced cardiotoxicity (Rahmatollahi et al., 2015).

Regulation of satiety, feeding and metabolism

Fu et al. (2003, 2005) first showed that the anorectic and weight-reducing effects of OEA were absent in PPARα knockout mice, and OEA administered daily reduced serum cholesterol levels in rat and mouse models of obesity. Guzman et al. (2004) also showed that the lipolytic effect of OEA in vivo was absent in PPARα knockout mice. Analogues of OEA with a high affinity for PPARα cause similar reductions in food intake (Astarita et al., 2006). The anorexic effects of OEA are mediated centrally by oxytocin signalling, which was absent in PPARα knockout mice (Gaetani et al., 2010; Romano et al., 2013). A peripherally restricted anandamide uptake inhibitor, AM404, also reduced feeding through a PPARα-dependent mechanism (Reyes-Cabello et al., 2012). More recently, a potential role for PPARγ has been identified in the regulation of leptin activity by CB₁ receptors in hypothalamic neurons (Palomba et al., 2015).

The anti-nausea effects of FAAH inhibition are mediated by PPARα (Rock et al., 2015). Interesting, while the effects of PF3845 were inhibited by a PPARα antagonist but not a CB₁ antagonist, the effects of URB597 were inhibited by a CB₁ receptor but not a PPARα antagonist, suggesting that these FAAH inhibitors are potentially causing a differential effects on endocannabinoid tone (albeit with the same end point of reduced nausea). No studies have yet examined whether PPARα plays a role in the anti-nausea effects of other cannabinoids.

Anti-inflammatory effects

The PPAR-mediated anti-inflammatory effects of some cannabinoids in the brain have already been outlined above, and there are many further studies showing PPAR-mediated anti-inflammatory effects of cannabinoids. This was probably first demonstrated by Liu et al. (2003) who showed that AJA inhibits the promoter activity of IL-8, a pro-inflammatory cytokine, in a PPARγ-dependent manner. AJA also inhibits skin fibrosis in mice overexpressing transforming growth factor β, sensitive to PPARγ antagonism (Gonzalez et al., 2012). Rockwell and Kaminski (2004) found that anandamide inhibits the secretion of the pro-inflammatory cytokine, IL-2, in a CB₁/CB₂ receptor-independent manner that could be prevented by a PPARγ antagonist. 2-AG also inhibited IL-2 secretion through the suppression of pro-inflammatory transcription factors, sensitive to PPARγ antagonism (Rockwell et al., 2006). 2-AG also decreases the expression of COX2 in response to IL-1β or LPS, sensitive to PPARγ antagonism (Du et al., 2011). Furthermore, the 2-AG metabolite 15d-PGJ₂-glycerol ester has anti-inflammatory actions mediated by PPARγ (Raman et al., 2011). Up-regulation of local endocannabinoid levels by inhibition of FAAH or inhibition of the putative anandamide transporter significantly potentiated the circulating cytokine response to LPS in rats, and this effect was reduced by antagonism of CB₁ and CB₂ receptors, TRPV1 channels and PPARγ (Roche et al., 2008).

Other studies have also demonstrated a role for PPARα in mediating the anti-inflammatory effects of some cannabinoids. Both OEA and PEA are anti-inflammatory in chemically induced oedema, which were absent in PPARα knockout mice (LoVerme et al., 2005). PEA also reduces inflammation, neutrophil infiltration, pro-inflammatory cytokines and NO synthase activity after spinal cord trauma, and this effect was absent in PPARα knockout mice and reduced by antagonism of PPARα and δ (Paterniti et al., 2013). PEA also decreases intestinal inflammation induced by ischaemia/reperfusion injury, which was reduced in PPARα knockout mice (Di Paola et al., 2012), and decreases the pathology of colitis in two different mouse models, which could be inhibited by CB₂ receptors, GPR55 and PPARα antagonists (Borrelli et al., 2015; Esposito et al., 2014). In an in vitro model of intestinal permeability induced by inflammation, we found that OEA and PEA were able to positively affect the hyperpermeability, which could be inhibited by PPARα antagonism (Karwad et al., 2014). In addition to the anti-inflammatory role of PPARα activation in the gut, another study has shown that the anti-inflammatory effects of CBD in the gastrointestinal system in LPS-treated mice are PPARγ mediated (De Filippis et al., 2011). Similarly, Hegde et al. (2015) showed that the anti-inflammatory effects of CBD via the induction of myeloid-derived suppressor cells were inhibited by PPARγ antagonism.

Physiological responses to cannabinoids that are PPAR independent

While there is evidence for PPAR activation by cannabinoids to be involved in many aspects of cannabinoid responses, there are studies equally demonstrating that PPAR activation does not underpin the effects of cannabinoids in their particular experimental model, as summarized in Table 3. At this stage, it is unclear as to why some physiological responses are mediated by PPARs for some cannabinoids and not others, despite an apparent similar ability to activate PPARs (Tables 1 and 2). For example, the effects of CBD at the BBB are inhibited by PPARγ antagonism (Hind et al., 2016), but the effects of anandamide are not (Hind et al., 2016), despite the fact that anandamide is known to activate PPARγ. Similarly, the effects of OEA and PEA on intestinal permeability are mediated by PPARα (Karwad et al., 2014), although the effects of anandamide and 2-AG in the same cells are not, instead acting via CB₁ (Alhamoruni et al., 2010, 2012). There are many factors that could be influencing the interactions between cannabinoids and PPARs. These include whether they also activate cell surface or other receptors, their metabolism, binding to FABPs and their intracellular fate, which FABP they preferentially bind and the recruitment of PPAR co-activators or repressors. All these many confounding factors require further investigation.

Table 3. Physiological responses to cannabinoids that known to be PPAR-independent

	Physiological response	Isoform not involved	Reference
Endocannabinoids
AEA	Modulation of intestinal permeability	PPARα or γ	Alhamoruni et al., 2010, 2012
	Reaction time tasks	PPARα	Panlilio et al., 2009
	Antiepileptic effect	PPARα	Citraro et al., 2013
	Modulation of BBB permeability	PPARα or γ	Hind et al., 2015
	Time-dependent vasorelaxant	PPARγ	Romano and Lograno, 2012
Endocannabinoid-like compounds
2-AG	Modulation of intestinal permeability	PPARα or γ	Alhamoruni et al., 2010, 2012
OEA	Upper GI transit	PPARα	Cluny et al., 2009
	Gastric emptying	PPARα	Aviello et al., 2008
	Modulation of cocaine-induced behaviour	PPARα	Bilbao et al., 2013
PEA	Neuroprotection	PPARγ	Koch et al., 2011; Scuderi et al., 2011; Scuderi et al., 2012
	Analgesia in neuropathic pain	PPARα	Costa et al., 2008
	Time-dependent vasorelaxant in the bovine ophthalmic artery	PPARγ	Romano and Lograno, 2012
	Intestinal motility	PPARα	Capasso et al., 2014
	Decreased contact dermatitis	PPARα	Petrosino et al., 2010
Noladin ether	Anti-proliferative effect	PPARγ	Nithipatikom et al., 2011
Increasing local activity of the endocannabinoid system
AM404	Decreased food intake	PPARα	Reyes-Cabello et al., 2012
URB597	Analgesia in an inflammatory pain model	PPARγ	Jhaveri et al., 2008
URB597	Anti-nausea effects	PPARα	Rock et al., 2015
Phytocannabinoids
THC	Modulation of intestinal permeability	PPARα or γ	Alhamoruni et al., 2010, 2012
CBD	Modulation of intestinal permeability	PPARα or γ	Alhamoruni et al., 2010, 2012
	Enhancement of vasorelaxation in diabetic arteries	PPARγ	Wheal et al., 2014
	Vasorelaxation of human small mesenteric arteries	PPARγ	Stanley et al., 2015
Synthetic cannabinoids
Methanandamide	Suppressed nicotine-induced excitation	PPARα	Melis et al., 2008
AJA	Anti-inflammatory effects	PPARγ	Johnson et al., 2007; Parker et al., 2008

AEA, anandamide; GI, Gastrointestinal; ECS, endocannabinoid system.

Conclusion

The aims of this review were to update the evidence that cannabinoids have “gone nuclear” and to establish whether activation by cannabinoids of the PPARs, a major class of nuclear hormone receptors, plays a role in their physiological effects (O'Sullivan, 2007; O'Sullivan, 2013). Although our knowledge in this area has significantly increased, there are still many cannabinoids whose activity at PPARs remains unknown. For example, there is little known about the effects of phytocannabinoids on PPARα and the potential role for PPARδ activation by cannabinoids. We do now know that many of the well-recognized responses to cannabinoids such as neuroprotection and analgesia are at least partly mediated by the activation of PPARs, although this is better investigated for some cannabinoids, such as OEA and PEA, than others. Despite the fact that anandamide and 2-AG bind to both PPARα and PPARγ, few studies have probed this as a mechanism of action for these endocannabinoids, possibly because much of the characterisation of these compounds was carried out before PPARs were proposed as additional targets of cannabinoids. Finally, there are also many PPAR-independent effects of cannabinoids, and the many factors that could be influencing the interactions between cannabinoids and PPARs remain to be established.

Conflict of interest

The author declares no conflicts of interest.

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Citing Literature

Volume173, Issue12

June 2016

Pages 1899-1910

An update on PPAR activation by cannabinoids

Abstract

Abbreviations

Tables of Links

Introduction

Evidence of PPAR activation by cannabinoids

Phytocannabinoids and their derivatives

Endocannabinoids and their derivatives

Synthetic cannabinoids

Cannabinoids, fatty acid binding proteins (FABPs) and PPARs

Physiological responses to cannabinoids mediated by PPARs

Neuroprotection

Reward

Memory and cognition

Analgesia

Anti-tumour effects of cannabinoids

Cardiovascular system

Regulation of satiety, feeding and metabolism

Anti-inflammatory effects

Physiological responses to cannabinoids that are PPAR independent

Conclusion

Conflict of interest

References

Citing Literature

References

Information

About Wiley Online Library

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An update on PPAR activation by cannabinoids

Abstract

Abbreviations

Tables of Links

Introduction

Evidence of PPAR activation by cannabinoids

Phytocannabinoids and their derivatives

Endocannabinoids and their derivatives

Synthetic cannabinoids

Cannabinoids, fatty acid binding proteins (FABPs) and PPARs

Physiological responses to cannabinoids mediated by PPARs

Neuroprotection

Reward

Memory and cognition

Analgesia

Anti-tumour effects of cannabinoids

Cardiovascular system

Regulation of satiety, feeding and metabolism

Anti-inflammatory effects

Physiological responses to cannabinoids that are PPAR independent

Conclusion

Conflict of interest

References

Citing Literature

References

Related

Information