Busch Lucila, Sterin-Borda Leonor, Borda Enri
School of Dentistry, University of Buenos Aires and Argentine National Research Council (CONICET), Buenos Aires, Argentina.
Clin Exp Pharmacol Physiol. 2006 Mar;33(3):258-63. doi: 10.1111/j.1440-1681.2006.04355.x.
In the present study, we examined whether cannabinoid receptor expression and the effects of receptor stimulation vary as a function of gonadal status in a peripheral tissue, namely the male rat parotid gland. Four groups of male rats were studied: gonadal intact, castrated, castrated testosterone (1 mg/100 g bodyweight) treated and gonadal intact testosterone treated. 2. The results showed that the density of CB(1) receptors decreased after castration and that receptor density was restored to control values after testosterone treatment. This decrement was associated with a decrease of anandamide (10(-10) to 10(-5) mol/L)-induced cAMP accumulation and amylase release without changes in the anandamide-induced inhibition of Na(+)/K(+)-ATPase activity. 3. Castration did not modify either the subtype of cannabinoid receptor involved in the actions of anandamide or drug affinity for the receptor. 4. The mechanism underlying anandamide-induced cAMP accumulation, amylase release and inhibition of Na(+)/K(+)-ATPase activity, namely through the activation of adenylyl cyclase, was the same in control and castrated rats. 5. Basal cAMP accumulation, amylase release and Na(+)/K(+)-ATPase activity were not altered by castration. 6. Castration had no effect on the concentration of total protein. 7. It can be concluded that CB(1) cannabinoid receptor expression is regulated by testosterone in male rat parotid gland and this has functional implications for cAMP accumulation and amylase release.
在本研究中,我们检测了大麻素受体表达以及受体刺激效应是否会随着性腺状态的变化而在一种外周组织(即雄性大鼠腮腺)中发生改变。我们研究了四组雄性大鼠:性腺完整组、去势组、去势后用睾酮(1毫克/100克体重)处理组以及性腺完整并用睾酮处理组。2. 结果显示,去势后CB(1)受体密度降低,而睾酮处理后受体密度恢复至对照值。这种降低与花生四烯酸乙醇胺(10^(-10)至10^(-5)摩尔/升)诱导的环磷酸腺苷(cAMP)积累及淀粉酶释放减少相关,而花生四烯酸乙醇胺诱导的钠钾ATP酶活性抑制未发生变化。3. 去势并未改变参与花生四烯酸乙醇胺作用的大麻素受体亚型,也未改变药物对该受体的亲和力。4. 在对照大鼠和去势大鼠中,花生四烯酸乙醇胺诱导cAMP积累、淀粉酶释放及抑制钠钾ATP酶活性的机制相同,即通过激活腺苷酸环化酶。5. 基础cAMP积累、淀粉酶释放及钠钾ATP酶活性不受去势影响。6. 去势对总蛋白浓度无影响。7. 可以得出结论,在雄性大鼠腮腺中,CB(1)大麻素受体表达受睾酮调节,这对cAMP积累和淀粉酶释放具有功能意义。