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Interactions of valerian extracts and a fixed valerian-hop extract combination with adenosine receptors.

机译:缬草提取物与固定的缬草蛇麻草提取物与腺苷受体的相互作用。

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摘要

Phytopharmaceuticals and dietary supplements containing valerian are used as mild sleep-inducing agents. An in vitro radioligand binding assay at A(1) and A(2A) adenosine receptors (ARs) was conducted with a fixed extract combination of valerian and hop (Ze 91019) to investigate a possible mechanism for the pharmacological activity of the extract. Component extracts of valerian and hop were also individually investigated. The fixed combination Ze 91019 as well as the valerian extracts therein exhibited selective affinity to A(1)ARs (K(i) = 0.15-0.37 mg/mL vs [3H]CCPA). The same extracts exhibited partial agonist activity at the A(1) adenosine receptor as indicated by a lower degree of stimulation of [35S]GTPgammaS binding in membrane preparations of CHO-hA(1) cells as compared to the full A(1) AR agonist N(6)-cyclopentyladenosine (CPA). In addition valerian extract inhibited cAMP accumulation in CHO-hA(1) cell membranes. The partial agonistic activity at A(1)ARs may thus play a role in the sleep inducing effect of Ze 91019 and the valerian extract therein.
机译:含有缬草的植物药物和膳食补充剂被用作轻度的睡眠诱导剂。用缬草和蛇麻草(Ze 91019)的固定提取物组合进行了A(1)和A(2A)腺苷受体(ARs)的体外放射性配体结合测定,以研究提取物的药理活性的可能机制。还分别研究了缬草和啤酒花的成分提取物。固定组合Ze 91019以及其中的缬草提取物表现出对A(1)ARs的选择性亲和力(相对于[3H] CCPA,K(i)= 0.15-0.37 mg / mL)。相同的提取物在A(1)腺苷受体上表现出部分激动剂活性,与完整A(1)AR相比,CHO-hA(1)细胞膜制剂中对[35S] GTPgammaS结合的刺激程度更低激动剂N(6)-环戊腺苷(CPA)。此外,缬草提取物抑制CHO-hA(1)细胞膜中的cAMP积累。因此,在A(1)ARs上的部分激动活性可能在Ze 91019和其中的缬草提取物的睡眠诱导作用中发挥作用。

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