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首页> 外文期刊>Clinical and experimental pharmacology & physiology >Effects of castration on cannabinoid cb receptor expression and on the biological actions of cannabinoid in the parotid gland.
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Effects of castration on cannabinoid cb receptor expression and on the biological actions of cannabinoid in the parotid gland.

机译:去势对大麻素cb受体表达和大麻素在腮腺中的生物学作用的影响。

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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.
机译:在本研究中,我们检查了大麻素受体的表达和受体刺激的作用是否根据性腺状态在周围组织即雄性大鼠腮腺中的变化而变化。研究了四组雄性大鼠:完整的性腺,去势的,去势的睾丸激素(1 mg / 100 g体重)和处理过的性腺完整的睾丸激素。 2.结果表明去势后CB(1)受体的密度降低,睾丸激素治疗后CB(1)受体的密度恢复到控制值。这种减少与anandamide(10(-10)到10(-5)mol / L)诱导的cAMP积累和淀粉酶释放相关,而anandamide诱导的Na(+)/ K(+)抑制作用没有改变-ATP酶活性。 3.去势没有改变参与anandamide作用的大麻素受体的亚型或对该受体的药物亲和力。 4.腺嘌呤诱导的cAMP积累,淀粉酶释放和Na(+)/ K(+)-ATPase活性抑制(即通过腺苷酸环化酶的激活)的潜在机制在对照和去势大鼠中相同。 5. cast割未改变基础cAMP积累,淀粉酶释放和Na(+)/ K(+)-ATPase活性。 6.去势对总蛋白浓度没有影响。 7.可以得出结论,雄性大鼠腮腺中的睾丸激素可调节CB(1)大麻素受体的表达,这对cAMP的积累和淀粉酶的释放具有功能意义。

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