Details

Autor(en) / Beteiligte

• Hiraoka, Yasuko
• Taniguchi, Takanobu
• Oshita, Masafumi
• Muramatsu, Ikunobu

Titel

Pharmacological Analysis of Neurogenic, Sympathetic Responses Mediated through Alpha-1-, Alpha-2-Adrenergic and Purinergic Receptors in the Dog Saphenous Vein

Ist Teil von

• Pharmacology, 2000-05, Vol.60 (4), p.188-194

Ort / Verlag

Basel, Switzerland: S. Karger AG

Erscheinungsjahr

2000

Link zum Volltext

Quelle

MEDLINE

Beschreibungen/Notizen

• Electrical transmural stimulation evoked a sympathetic contraction in the isolated dog saphenous vein. This contraction consisted of three components (α1-adrenergic, α2-adrenergic and purinergic), which were separately observed under combined treatments either with yohimbine (blockade of α2-adrenoceptor) and α,β-methylene ATP (desensitization of P2X-purinoceptors), with prazosin (blockade of α1-adrenoceptor) and α,β-methylene ATP, or with prazosin and yohimbine, respectively. The α1-adrenergic and purinergic contractions immediately developed after the start of stimulation and reached a peak rapidly. In contrast, the α2-adrenergic contraction developed slowly, thus the time to peak contraction was longer than the other two components. The relationship between the peak amplitudes of contraction and stimulus frequencies were similar between α1- and α2-adrenergic components, but the purinergic contraction was smaller than the other components at all frequencies (0.1–30 Hz). Cocaine, a neuronal uptake inhibitor of noradrenaline, significantly potentiated α1- and α2-adrenergic components and prolonged their duration with a relatively greater effect on the α2-adrenergic component. In contrast, the purinergic component was not affected by cocaine. Exogenous noradrenaline produced concentration-dependent contraction, which was inhibited more effectively after combined treatment with combination of prazosin and yohimbine than either blocker given alone. Cocaine potentiated the attenuated contractile response to noradrenaline in the presence of prazosin, resulting in the recovery of response to the control level. Exogenous ATP produced a transient contraction, which was abolished under conditions where postjunctional P2X-purinoceptors were desensitized with α,β-methylene ATP. Cocaine did not affect the ATP-induced contraction. These results suggest that sympathetic contraction of the dog saphenous vein is caused through three distinct routes (α1- and α2-adrenoceptors and P2X-purinoceptors).