2012
DOI: 10.1016/j.joen.2012.02.025
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Anandamide Induces Matrix Metalloproteinase-2 Production through Cannabinoid-1 Receptor and Transient Receptor Potential Vanilloid-1 in Human Dental Pulp Cells in Culture

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Cited by 24 publications
(21 citation statements)
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“…(ii) TRPV1 is co-localized with CB1 and CB2 in cerebromicrovascular endothelial cells [62] and with CB1 in endothelial cells from mesenteric arteries of cirrhotic rats [63,64]; (iii) TRPV1 is co-localized with both CB1 and CB2 in mouse bone-marrowderived dendritic cells [65], and in human skeletal muscle cells [66], myometrial smooth muscle cells [67], osteoclasts [68], proximal tubular (HK2) cells of the kidney [69], keratinocytes [70,71], melanocytes [72] and dental pulp cells [73]; (iv) TRPV1 is co-localized only with CB1 in human sperm cells [74], and only with CB2 in synoviocytes from rats after intraarticular injection of mono-iodo-acetate, a model of osteoarthritis [75]. In view of the previously reported cross-talk between TRPV1 and CB1 receptors at the level of down-stream signalling events [76,77], these many examples of co-expression between the channel and one or both cannabinoid receptor sub-types offer the opportunity of widening further the range of pharmacological effects that endogenous mediators capable of activating both types of receptors may have, and, hence, the extent of 'plasticity' that their action can produce in a large variety of biological systems.…”
Section: Co-expression Of Cb1 or Cb2 Receptors And Trpv1 Channels In mentioning
confidence: 99%
“…(ii) TRPV1 is co-localized with CB1 and CB2 in cerebromicrovascular endothelial cells [62] and with CB1 in endothelial cells from mesenteric arteries of cirrhotic rats [63,64]; (iii) TRPV1 is co-localized with both CB1 and CB2 in mouse bone-marrowderived dendritic cells [65], and in human skeletal muscle cells [66], myometrial smooth muscle cells [67], osteoclasts [68], proximal tubular (HK2) cells of the kidney [69], keratinocytes [70,71], melanocytes [72] and dental pulp cells [73]; (iv) TRPV1 is co-localized only with CB1 in human sperm cells [74], and only with CB2 in synoviocytes from rats after intraarticular injection of mono-iodo-acetate, a model of osteoarthritis [75]. In view of the previously reported cross-talk between TRPV1 and CB1 receptors at the level of down-stream signalling events [76,77], these many examples of co-expression between the channel and one or both cannabinoid receptor sub-types offer the opportunity of widening further the range of pharmacological effects that endogenous mediators capable of activating both types of receptors may have, and, hence, the extent of 'plasticity' that their action can produce in a large variety of biological systems.…”
Section: Co-expression Of Cb1 or Cb2 Receptors And Trpv1 Channels In mentioning
confidence: 99%
“…For example, SR141716 (also known as rimonabant) has been shown to act both as a CB1R antagonist and as an inverse agonist (Table 1) (15,72). Notably, endocannabinoids can also mediate some of their biological effects through alternative molecular targets such as the orphan G proteincoupled receptor GPR55 or the transient receptor potential cation channel (TRPV1) (90,127).…”
mentioning
confidence: 99%
“…CB1 is also reportedly expressed in human odontoblasts (Que et al, 2017). It can accelerate the formation of "reparative dentin" in rat odontoblasts by modulating extracellular Ca 2+ entry (Tsumura et al, 2012) and may be involved in dental pulp tissue repair by regulating matrix metalloproteinase-2 in dental pulp cells (Miyashita, Oyama, Sakuta, Tokuda, & Torii, 2012). The role of cannabinoid regulation of pulp pain and dentin repair/regeneration needs further investigation.…”
Section: Pulp Tissuementioning
confidence: 99%