Prestifilippo Juan Pablo, Fernández-Solari Javier, de la Cal Carolina, Iribarne María, Suburo Angela M, Rettori Valeria, McCann Samuel M, Elverdin Juan Carlos
Centro de Estudios Farmacológicos y Botánicos (CEFYBO-CONICET) (ex CIBIER), Paraguay 2155, piso 16, Ciudad de Buenos Aires, Buenos Aires 1121, Argentina.
Exp Biol Med (Maywood). 2006 Sep;231(8):1421-9. doi: 10.1177/153537020623100816.
It is known that marijuana use decreases saliva secretion. Therefore, we hypothesized that cannabinoid receptors (CBs) are located in salivary glands to mediate that effect. In these experiments, we used the submandibular gland (SMG) of male rats, which is one of the major salivary glands. Mammalian tissues contain at least two types of CBs, CB1 and CB2, mainly located in the nervous system and peripheral tissues, respectively. Both receptors are coupled to Gi protein and respond by inhibiting the activity of adenylyl cyclase. We demonstrated that both CB1 and CB2 are present in the SMG, each showing specific localizations. The best-known endocannabinoid is anandamide (AEA), which binds with high affinity to CB1 and CB2. We showed that AEA markedly reduced forskolin-induced increase of cAMP content in vitro. This effect was blocked by AM251 and AM630 (CB1 and CB2 antagonists, respectively), indicating that both receptors are implicated in SMG physiology. In addition, we showed that AEA injected intraglandularly to anesthetized rats inhibited norepinephrine (NE)- and methacholine (MC)-stimulated saliva secretion in vivo and that both AM251 or AM630 prevented the inhibitory action of AEA. Also, the intraglandular injection of AM251 increased saliva secretion induced by lower doses of NE or MC. This increase was synergized after coinjection with AM630. Therefore, we concluded that AEA decreases saliva secretion in the SMG acting through CB1 and CB2 receptors.
已知使用大麻会减少唾液分泌。因此,我们推测大麻素受体(CBs)位于唾液腺中以介导这种效应。在这些实验中,我们使用了雄性大鼠的下颌下腺(SMG),它是主要的唾液腺之一。哺乳动物组织至少含有两种类型的CBs,即CB1和CB2,分别主要位于神经系统和外周组织中。两种受体都与Gi蛋白偶联,并通过抑制腺苷酸环化酶的活性作出反应。我们证明CB1和CB2都存在于SMG中,各自表现出特定的定位。最著名的内源性大麻素是花生四烯乙醇胺(AEA),它与CB1和CB2具有高亲和力结合。我们表明,AEA在体外显著降低了福斯可林诱导的cAMP含量增加。这种效应被AM251和AM630(分别为CB1和CB2拮抗剂)阻断,表明两种受体都参与了SMG的生理功能。此外,我们表明,向麻醉大鼠腺内注射AEA在体内抑制了去甲肾上腺素(NE)和乙酰甲胆碱(MC)刺激的唾液分泌,并且AM251或AM630都能阻止AEA的抑制作用。同样,腺内注射AM251增加了低剂量NE或MC诱导的唾液分泌。与AM630联合注射后,这种增加产生了协同作用。因此,我们得出结论,AEA通过CB1和CB2受体作用降低SMG中的唾液分泌。