Methylhonokiol attenuates neuroinflammation: a role for cannabinoid receptors?
- 19k Downloads
The cannabinoid type-2 G protein-coupled (CB2) receptor is an emerging therapeutic target for pain management and immune system modulation. In a mouse model of Alzheimer’s disease (AD) the orally administered natural product 4′-O-methylhonokiol (MH) has been shown to prevent amyloidogenesis and progression of AD by inhibiting neuroinflammation. In this commentary we discuss an intriguing link between the recently found CB2 receptor-mediated molecular mechanisms of MH and its anti-inflammatory and protective effects in AD animal models. We argue that the novel cannabimimetic MH may exert its beneficial effects via modulation of CB2 receptors expressed in microglial cells and astrocytes. The recent findings provide further evidence for a potential role of CB2 receptors in the pathophysiology of AD, spurring target validation and drug discovery.
KeywordsAlzheimer’s disease Cannabinoids CB2 receptors Endocannabinoid System Magnolia grandiflora Medicinal plant Methylhonokiol
Cannabinoid type-1 receptor
Cannabinoid type-2 G protein-coupled receptor
Central nervous system
Mitogen-activated protein kinases
Nuclear factor kappa B
Tumor necrosis factor alpha.
In a recent study published in Journal of Neuroinflammation Lee and colleagues report that the natural product 4′-O-methylhonokiol (MH) from Magnolia grandiflora L. potently inhibits lipopolysaccharide (LPS)-induced amyloidogenesis via anti-inflammatory mechanisms . They have shown that chronic oral administration of 1 mg/kg of MH in mice strongly ameliorates LPS-induced memory impairment via inhibition of nuclear factor kappa B (NF-κB) and the gene expression of inducible nitric oxide synthase and cyclooxygenase-2. MH also inhibited the activation of astrocytes in the brain. The same group recently reported that MH attenuates the development of Alzheimer’s disease (AD) in Tg2576 mice , and inhibits different signaling cascades related to oxidative stress and mitogen-activated protein (MAP) kinases [3, 4, 5]. In the European patent application EP2327402A2 by Bioland Ltd. the authors report the invention of a method for treating or preventing amyloid-related diseases comprising administering a pharmaceutically effective dosage of MH or pharmaceutically acceptable salt thereof . In this patent it is mentioned that MH inhibits acetylcholinesterase (AChE) and in a subsequent study it was shown that MH inhibits AChE activity at nM concentrations in vitro. In yet another study by the same group, MH was shown to inhibit hydrogen peroxide and Aβ(1-42)-induced neurotoxicity in cultured neurons, as well as PC12 cells, by prevention of the reactive oxygen species generation and directly inhibited β-secretase activity and Aβ fibrilization in vitro. Thus, MH could be a useful agent to prevent the neuroinflammation-associated pathogenesis or the progression of AD. However, beyond the AChE inhibition, none of the studies describe any molecular interaction of MH and its anti-inflammatory mechanism of action therefore remains elusive. In their article, Lee et al. suggested that inhibition of NF-κB and MAP kinases or the general antioxidative properties of MH are potential mechanisms by which this biphenyl natural product inhibits inflammation and amyloidogenesis . However, from the data presented it is not clear whether the inhibition of signaling is a primary or secondary event, for example to receptor modulation. Moreover, some signaling effects were only observed at high nM or even μM concentrations in vitro which do not necessarily reflect the physiological concentrations in the brain. We therefore comment on a recently discovered molecular mechanism of action of MH that could well explain some of the anti-inflammatory effects observed.
MH is a novel modulator of CB2 receptors and inflammation
In a previous study we have shown that MH is a potent and selective cannabinoid type-2 G protein-coupled (CB2) receptor ligand (hCB2Ki = 44 nM), triggering a novel type of heteroactive signaling (EC50 ~ 10 nM) . In an in vitro profiling comprising more than 40 receptors MH was highly specific towards cannabinoid CB2 receptors at nM concentrations. Furthermore, MH did not interact with cannabinoid type-1 (CB1) receptors, which in the brain are predominantly expressed in neurons, and found in presynaptic sites of GABAergic and glutamatergic synapses where they in a retrograde manner inhibit the release of these neurotransmitters [10, 11, 12]. Whereas CB1 receptors mainly mediate the central side effects of cannabinoids, CB2 receptors are primarily associated with a broad range of inflammatory processes [13, 14, 15, 16]. CB2 receptors are largely absent in the central nervous system (CNS) under normal conditions, but are upregulated in microglial cells and astrocytes under neuroinflammatory stimulation as it occurs in AD [17, 18]. Indeed, CB2 receptors appear to mediate many of the anti-inflammatory actions of endocannabinoids, the arachidonic acid-derived lipids which non-specifically target cannabinoid receptors [19, 20]. There is an overall agreement that endocannabinoids are released during oxidative and inflammatory stress and counterbalance inflammation by inducing a TH1-TH2 cytokine shift, although the exact mechanisms are not understood [14, 21, 22]. In our study we have shown that MH potently inhibits LPS-stimulated TNF-α expression and chemotaxis in macrophages in an apparently CB2 receptor-dependent manner, exerting anti-inflammatory and anti-osteoclastogenic effects .
A role for CB2 receptors in the pathophysiology of AD
The endocannabinoid system and neuroinflammation
Although AD is currently treated with cholinergic and glutamatergic therapies, which provide symptomatic benefit, the pathophysiology of AD is also widely associated with inflammation and aberrations of innate immunity . Inflammation is not only involved in acute CNS conditions, such as stroke and traumatic injury, but it is also a central factor in chronic and neurodegenerative conditions such as AD, Parkinson’s disease and multiple sclerosis . Nevertheless, the inflammation hypothesis of AD, as attractive as it appears, has not yet been corroborated in clinical trials. Recent attempts to treat AD with non-steroidal anti-inflammatory drugs and the TNF-α blocker entanercept were not successful [38, 39], most probably due to the fundamental biochemical differences between neuroinflammation and peripheral inflammation . However, novel pleiotropic anti-inflammatory mechanisms based on modulation of innate immunity, including the modulation of the endocannabinoid system, may be exploited. Because the CB2 receptor mediates different anti-inflammatory effects via multiple signaling pathways  it was previously suggested to be a drug target to treat neurodegenerative diseases [17, 31]. However, to date only few preclinical studies have explored the pharmacological effects of the distinctly different CB2 receptor ligands (full agonists, partial agonists, inverse agonists, silent antagonists and protean agonists) in models of neuroinflammation and AD.
CB2 receptor modulation by MH to target AD?
The promising preclinical results obtained with the novel CB2 receptor ligand MH may spur further research on the role of CB2 receptors in neuroinflammation in general and AD in particular. The findings reported by Lee et al.  are intriguing because they clearly indicate that MH is orally bioavailable to the CNS in mice, as well as active at relatively low doses. This is unexpected given the likely detoxification and phase II biotransformation of the biphenyl scaffold of this neolignan . Thus, until the pharmacokinetics and metabolism of MH are studied it cannot be excluded that MH may potentially also act as a prodrug. Alternatively, MH crosses the blood–brain barrier and reaches the nM concentrations necessary to inhibit AChE and to modulate CB2 receptors, thus exerting a polypharmacological action on acetylcholine levels and inflammation. In addition to downregulating cyclooxygenase-2 gene expression , MH also directly inhibits COX1/2 , which may further contribute to its in vivo efficacy. MH is a relatively rare natural product of plant origin which is mainly found in the seeds of M. grandiflora, a tree native to Northern Mexico and the USA [43, 44]. Its long use in traditional medicine and its mention in the United States Pharmacopoia as antimalarial and diaphoretic [44, 45] suggest a lack of acute toxicity of MH, a major secondary metabolite in this medicinal plant.
Because of the promising preclinical studies reported in the past, further studies are indicated to explore the therapeutic potential of CB2 receptor modulators such as MH and its CB2 receptor active derivatives  for AD drug discovery.
JG is a professor and research PI at the Institute of Biochemistry and Molecular Medicine (IBMM), National Centre of Competence in Research NCCR TransCure, University of Bern, Switzerland. His research interests focus on the endocannabinoid system, molecular pharmacology and chemical biology, with an interest in natural products and drug discovery. SAG is a senior researcher and lecturer at the Departments of Behavioral Sciences and Molecular Biology, Ariel University Centre of Samaria, Israel. Her current research interests focus on the role of the endocannabinoid system in behavior and molecular pharmacology.
We thank Stefanie Hofer-Reyes for proofreading the manuscript.
- 1.Lee YJ, Choi DY, Choi IS, Kim KH, Kim YH, Kim HM, Lee K, Cho WG, Jung JK, Han SB, Han JY, Nam SY, Yun YW, Jeong JH, Oh KW, Hong JT: Inhibitory effect of 4-O-methylhonokiol on lipopolysaccharide-induced neuroinflammation, amyloidogenesis and memory impairment via inhibition of nuclear factor-kappaB in vitro and in vivo models. J Neuroinflammation 2012, 9:35.CrossRefPubMedPubMedCentralGoogle Scholar
- 2.Lee YJ, Choi DY, Lee YK, Lee YM, Han SB, Kim YH, Kim KH, Nam SY, Lee BJ, Kang JK, Yun YW, Oh KW, Hong JT: 4-O-methylhonokiol prevents memory impairment in the Tg2576 Transgenic Mice Model of Alzheimer’s disease via regulation of β-Secretase activity. J Alzheimers Dis 2012, 29:677–690.PubMedGoogle Scholar
- 3.Choi IS, Lee YJ, Choi DY, Lee YK, Lee YH, Kim KH, Kim YH, Jeon YH, Kim EH, Han SB, Jung JK, Yun YP, Oh KW, Hwang DY, Hong JT: 4-O-methylhonokiol attenuated memory impairment through modulation of oxidative damage of enzymes involving amyloid-β generation and accumulation in a mouse model of Alzheimer’s disease. J Alzheimers Dis 2011, 27:127–141.PubMedGoogle Scholar
- 4.Lee YJ, Choi IS, Park MH, Lee YM, Song JK, Kim YH, Kim KH, Hwang DY, Jeong JH, Yun YP, Oh KW, Jung JK, Han SB, Hong JT: 4-O-Methylhonokiol attenuates memory impairment in presenilin 2 mutant mice through reduction of oxidative damage and inactivation of astrocytes and the ERK pathway. Free Radic Biol Med 2011, 50:66–77.CrossRefPubMedGoogle Scholar
- 7.Lee YK, Yuk DY, Kim TI, Kim YH, Kim KT, Kim KH, Lee BJ, Nam SY, Hong JT: Protective effect of the ethanol extract of Magnolia officinalis and 4-O-methylhonokiol on scopolamine-induced memory impairment and the inhibition of acetylcholinesterase activity. J Nat Med 2009, 63:274–282.CrossRefPubMedPubMedCentralGoogle Scholar
- 15.Pertwee RG, Howlett AC, Abood ME, Alexander SP, Di Marzo V, Elphick MR, Greasley PJ, Hansen HS, Kunos G, Mackie K, Mechoulam R, Ross RA: International Union of Basic and Clinical Pharmacology. LXXIX. Cannabinoid receptors and their ligands: beyond CB1 and CB2. Pharmacol Rev 2010, 62:588–631.CrossRefPubMedPubMedCentralGoogle Scholar
- 23.Palazuelos J, Davoust N, Julien B, Hatterer E, Aguado T, Mechoulam R, Benito C, Romero J, Silva A, Guzmán M, Nataf S, Galve-Roperh I: The CB(2) cannabinoid receptor controls myeloid progenitor trafficking: involvement in the pathogenesis of an animal model of multiple sclerosis. J Biol Chem 2008, 283:13320–13329.CrossRefPubMedGoogle Scholar
- 32.Benito C, Tolón RM, Castillo AI, Ruiz-Valdepeñas L, Martínez-Orgado JA, Fernández-Sánchez FJ, Vázquez C, Cravatt BF, Romero J: Beta amyloid exacerbates inflammation in astrocytes lacking fatty acid amide hydrolase through a mechanism involving Ppar-α, Ppar-γ and Trpv1, but not Cb(1) or Cb(2) Receptors. Br J Pharmacol 2012, 166:1474–1489.CrossRefPubMedPubMedCentralGoogle Scholar
- 35.Chao LK, Liao PC, Ho CL, Wang EI, Chuang CC, Chiu HW, Hung LB, Hua KF: Anti-inflammatory bioactivities of honokiol through inhibition of protein kinase C, mitogen- activated protein kinase, and the NF-kappaB pathway to reduce LPS-induced TNFalpha and NO expression. J Agric Food Chem 2010, 58:3472–3478.CrossRefPubMedGoogle Scholar
- 37.Eikelenboom P, Veerhuis R, van Exel E, Hoozemans JJ, Rozemuller AJ, van Gool WA: The early involvement of the innate immunity in the pathogenesis of late-onset Alzheimer’s disease: neuropathological, epidemiological and genetic evidence. Curr Alzheimer Res 2011, 8:142–50.CrossRefPubMedGoogle Scholar
- 42.Schühly W, Hüfner A, Pferschy-Wenzig EM, Prettner E, Adams M, Bodensieck A, Kunert O, Oluwemimo A, Haslinger E, Bauer R: Design and synthesis of ten biphenyl-neolignan derivatives and their in vitro inhibitory potency against cyclooxygenase-1/2 activity and 5-lipoxygenase-mediated LTB4-formation. Bioorg Med Chem 2009, 17:4459–4465.CrossRefPubMedGoogle Scholar
- 43.Martinez M: Las plantas medicinales de Mexico. 4th edition. Editorial Botas, Mexico City; 1959:343–347.Google Scholar
- 44.Ahmed SM, Abdelaleil AM: Antifungal activity of extracts and sesquiterpene lactones from Magnolia grandiflora L, (Magnoliaceae). Int J Agric Biol 2005, 7:638–642.Google Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.