Zamfirova R, Todorov S
Institute of Physiology, Bulgarian Academy of Sciences, Sofia.
Methods Find Exp Clin Pharmacol. 1988 Nov;10(11):683-6.
The effects of substance P (SP) on smooth-muscle contractions induced by noradrenaline (NA) or by high- or low-frequency electrical stimulation (ES) were studied on isolated rat vas deferens and musculus anococcygeus. Neither the contractile effects of NA nor those of high-frequency ES were significantly changed by SP. The peptide in concentrations of 1 x 10(-7) M and 1 x 10(-6) M strongly potentiated (up to 70%) vas deferens contractions in response to low-frequency ES but slightly reduced those of musculus anococcygeus. Inhibition of the opiate receptors by 1 x 10(-6) M naloxone did not change the potentiating SP-effect on vas deferens contractions. Blockade of the prostaglandin (PG) receptors by polyphloretin phosphate (PPP), 5 micrograms/ml, or of the PGs synthesis by indomethacin, 5 x 10(-6) M, resulted in a slight increase of the SP-potentiating effect. The present results suggest that specific presynaptic SP-receptors (excitatory or inhibitory) play a major role in the mechanism of the potentiating action of substance P.
研究了P物质(SP)对去甲肾上腺素(NA)或高频或低频电刺激(ES)诱导的大鼠离体输精管和尾骨肌平滑肌收缩的影响。SP对NA的收缩作用以及高频ES的收缩作用均无显著改变。浓度为1×10⁻⁷ M和1×10⁻⁶ M的该肽可强烈增强(高达70%)输精管对低频ES的收缩反应,但对尾骨肌的收缩反应略有减弱。1×10⁻⁶ M纳洛酮对阿片受体的抑制并未改变SP对输精管收缩的增强作用。5微克/毫升的聚磷酸根皮苷(PPP)对前列腺素(PG)受体的阻断或5×10⁻⁶ M消炎痛对PG合成的阻断,导致SP增强作用略有增加。目前的结果表明,特定的突触前SP受体(兴奋性或抑制性)在P物质增强作用机制中起主要作用。