Chen Y F, Lin Y T, Tan T W, Tsai H Y
Department of Pharmacology and Institute of Pharmaceutical Sciences, China Medical College, Taichung, Taiwan, ROC.
Phytomedicine. 2002 May;9(4):296-301. doi: 10.1078/0944-7113-00122.
In this study, we attempted to identify the interactions and mechanisms between veratrine and paeoniflorin on isolated mouse vas deferens. Paeoniflorin had no effect on isolated mouse vas deferens. Veratrine (1 x 10(-5) approximately 1 x 10(-3) g/ml) could directly induce contraction of isolated rat and mouse vas deferens. The concentration induced by veratrine (1 x 10(-5) g/ml) was completely inhibited by Ca2+-free solution and verapamil (1 x 10(-5) M), in both the epididymal and the prostatic portions of isolated mouse vas deferens. Naloxone (1 x 10(-5) M) did not alter the contraction induced by veratrine (1 x 10(-5) g/ml) in either the epididymal or the prostatic portions of isolated mouse vas deferens. Paeoniflorin (4.8 x 10(-5) g/ml) inhibited the contraction induced by veratrine (1 x 10(-5) g/ml) in both the epididymal and the prostatic portions of isolated mouse vas deferens. Paeoniflorin (4.8 x 10(-5) g/ml) potentiated norepinephrine (1 x 10(-5) M)-induced phasic contraction in the epididymal portion, but decreased contractions in the prostatic portion. Paeoniflorin (4.8 x 10(-5) g/ml) increased KCI (56 mM)-induced phasic contraction in the epididymal portion, but decreased the tonic contraction in either the epididymal or the prostatic portion. Veratrine (1 x 10(-5) g/ml)-induced contractions could be decreased by pretreatment with ryanodine (1 x 10(-5) M) in both the epididymal and the prostatic portions. Pretreatment with the combination of paeoniflorin (4.8 x 10(-5) g/ml) and ryanodine (1 x 10(-5) M) did not potentiate the inhibition of paeoniflorin in the veratrine-induced contraction in both the epididymal and the prostatic portions of isolated mouse vas deferens.
在本研究中,我们试图确定藜芦碱和芍药苷对分离的小鼠输精管的相互作用及机制。芍药苷对分离的小鼠输精管无作用。藜芦碱(1×10⁻⁵~1×10⁻³g/ml)可直接诱导分离的大鼠和小鼠输精管收缩。在分离的小鼠输精管的附睾段和前列腺段,藜芦碱(1×10⁻⁵g/ml)诱导的收缩均被无钙溶液和维拉帕米(1×10⁻⁵M)完全抑制。纳洛酮(1×10⁻⁵M)对分离的小鼠输精管附睾段或前列腺段由藜芦碱(1×10⁻⁵g/ml)诱导的收缩均无影响。芍药苷(4.8×10⁻⁵g/ml)在分离的小鼠输精管附睾段和前列腺段均抑制藜芦碱(1×10⁻⁵g/ml)诱导的收缩。芍药苷(4.8×10⁻⁵g/ml)增强去甲肾上腺素(1×10⁻⁵M)诱导的附睾段的相性收缩,但减弱前列腺段的收缩。芍药苷(4.8×10⁻⁵g/ml)增加氯化钾(56mM)诱导的附睾段的相性收缩,但减弱附睾段或前列腺段的强直性收缩。在分离的小鼠输精管附睾段和前列腺段,用ryanodine(1×10⁻⁵M)预处理可减弱藜芦碱(1×10⁻⁵g/ml)诱导的收缩。用芍药苷(4.8×10⁻⁵g/ml)和ryanodine(1×10⁻⁵M)联合预处理在分离的小鼠输精管附睾段和前列腺段均未增强芍药苷对藜芦碱诱导收缩的抑制作用。