کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1982568 | 1539510 | 2009 | 6 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Comparative pharmacology of two D1-like dopamine receptors cloned from the silkworm Bombyx mori Comparative pharmacology of two D1-like dopamine receptors cloned from the silkworm Bombyx mori](/preview/png/1982568.png)
Dopamine (DA) is a physiologically important biogenic amine in insect peripheral and nervous tissues. We recently cloned two DA receptors (BmDopR1 and BmDopR2) from the silkworm Bombyx mori and identified them as D1-like receptors, which activate adenylate cyclase to increase intracellular cAMP levels. In this study, these two receptors were stably expressed in HEK-293 cells, and the dose-responsiveness to DA and their pharmacological properties were examined using cAMP assays. BmDopR1 showed a dose-dependent increase in cAMP levels at DA concentrations up to 10−7 M with EC50 of 3.30 nM, while BmDopR2 required 10−6 M DA for activation. In BmDopR1-expressing cells, DA at 10−6–10−4 M induced 30–50% lower cAMP production than 10−7 M DA. BmDopR2-expressing cells showed a standard sigmoidal dose–response, with maximum cAMP levels attained with 10−5–10−4 M DA and EC50 of 1.30 μM. Both receptors had similar agonist profiles, and the typical vertebrate D1-like receptor agonist SKF-38393 was ineffective. Experiments with antagonists revealed that BmDopR1 exhibits D1-like features. However, the pharmacology of BmDopR2 was distinct from D1-like receptors; the typical vertebrate D1-like receptor antagonist SCH-23390 was less potent than the nonselective antagonist flupenthixol and the D2-like receptor antagonist chlorpromazine. The rank order of activities of several antagonists for BmDopR1 and BmDopR2 was more similar to that of Drosophila melanogaster DA receptors than Apis mellifera DA receptors. These data suggest that DA receptors could be potential targets for specific insecticides or insectistatics.
Journal: Insect Biochemistry and Molecular Biology - Volume 39, Issues 5–6, May–June 2009, Pages 342–347