中国药物与临床
中國藥物與臨床
중국약물여림상
CHINESE REMEDIES & CLINICS
2014年
8期
1009-1011
,共3页
秦小江%侯晓敏%梁泰刚
秦小江%侯曉敏%樑泰剛
진소강%후효민%량태강
钙通道,L型%肾动脉%大鼠%白杨素
鈣通道,L型%腎動脈%大鼠%白楊素
개통도,L형%신동맥%대서%백양소
Calcium channels,L-type%Renal artery%Rats%Chrysin
目的研究白杨素对大鼠离体肾动脉的舒张作用及其机制是否涉及抑制肾动脉血管平滑肌细胞L-型电压依赖性钙通道。方法利用微血管张力记录仪(DMT)观察白杨素对预收缩大鼠肾动脉血管环的肌源性反应;利用全细胞膜片钳电生理学实验方法,观察白杨素对大鼠离体肾动脉血管平滑肌细胞L-型电压依赖性钙电流的作用。结果①白杨素浓度依赖性的舒张60 mmol/L KCl或10-5 mol/L去氧肾上腺素(PE)预收缩的大鼠肾动脉血管环,其最大舒张幅度分别为88.99%和67.47%,RC50值分别为26.25μmol/L和51.68μmol/L。②白杨素(浓度为RC50值)可抑制大鼠肾动脉血管平滑肌细胞L-型电压依赖性钙电流,使其I-V曲线非平行上移;给予0 mV单电压刺激时,白杨素(浓度为RC50值)使大鼠肾动脉血管平滑肌细胞L-型电压依赖性钙电流值降低45.43%。结论①白杨素浓度依赖性舒张60 mmol/L KCl或10-5 mol/L PE预收缩的大鼠肾动脉血管环;②白杨素抑制大鼠肾动脉血管平滑肌细胞L-型电压依赖性钙电流,使其I-V曲线非平行上移。
目的研究白楊素對大鼠離體腎動脈的舒張作用及其機製是否涉及抑製腎動脈血管平滑肌細胞L-型電壓依賴性鈣通道。方法利用微血管張力記錄儀(DMT)觀察白楊素對預收縮大鼠腎動脈血管環的肌源性反應;利用全細胞膜片鉗電生理學實驗方法,觀察白楊素對大鼠離體腎動脈血管平滑肌細胞L-型電壓依賴性鈣電流的作用。結果①白楊素濃度依賴性的舒張60 mmol/L KCl或10-5 mol/L去氧腎上腺素(PE)預收縮的大鼠腎動脈血管環,其最大舒張幅度分彆為88.99%和67.47%,RC50值分彆為26.25μmol/L和51.68μmol/L。②白楊素(濃度為RC50值)可抑製大鼠腎動脈血管平滑肌細胞L-型電壓依賴性鈣電流,使其I-V麯線非平行上移;給予0 mV單電壓刺激時,白楊素(濃度為RC50值)使大鼠腎動脈血管平滑肌細胞L-型電壓依賴性鈣電流值降低45.43%。結論①白楊素濃度依賴性舒張60 mmol/L KCl或10-5 mol/L PE預收縮的大鼠腎動脈血管環;②白楊素抑製大鼠腎動脈血管平滑肌細胞L-型電壓依賴性鈣電流,使其I-V麯線非平行上移。
목적연구백양소대대서리체신동맥적서장작용급기궤제시부섭급억제신동맥혈관평활기세포L-형전압의뢰성개통도。방법이용미혈관장력기록의(DMT)관찰백양소대예수축대서신동맥혈관배적기원성반응;이용전세포막편겸전생이학실험방법,관찰백양소대대서리체신동맥혈관평활기세포L-형전압의뢰성개전류적작용。결과①백양소농도의뢰성적서장60 mmol/L KCl혹10-5 mol/L거양신상선소(PE)예수축적대서신동맥혈관배,기최대서장폭도분별위88.99%화67.47%,RC50치분별위26.25μmol/L화51.68μmol/L。②백양소(농도위RC50치)가억제대서신동맥혈관평활기세포L-형전압의뢰성개전류,사기I-V곡선비평행상이;급여0 mV단전압자격시,백양소(농도위RC50치)사대서신동맥혈관평활기세포L-형전압의뢰성개전류치강저45.43%。결론①백양소농도의뢰성서장60 mmol/L KCl혹10-5 mol/L PE예수축적대서신동맥혈관배;②백양소억제대서신동맥혈관평활기세포L-형전압의뢰성개전류,사기I-V곡선비평행상이。
Objective To investigate the vasodilatory effects of chrysin on ex-vivo rat renal artery and to deter-mine the association with L-type voltage-dependent calcium channel in the arterial smooth muscle cells. Methods By utilizing the DMT microvessle tension recorder, we assessed the muscular responses of rat renal arterial ring to chrysin. Whole-cell membrane clamp was employed to determine the electrophysiology properties of the arterial smooth muscle cells. This allowed the assessment of the effects of chrysin on arterial smooth muscle cell L-type volt-age-dependent calcium channel-mediate currents in rats in vitro. Results Chrysin dilated the renal arterial ring pre-treated with 60 mmol/L KCl or 10-5 mol/L PE in a concentration-dependent fashion. The maximal magnitude of dilation was 88.99%and 67.47%, corresponding to the RC50 of 26.25 μmol/L and 51.68 μmol/L. Chrysin administered at the concentration of the RC50 abolished the renal arterial smooth muscle cell L-type voltage-dependent calcium channel-mediated current and resulted in a non-linear up-shift of the I-V curve. When stimulated with electric voltage of 0 mV, there was a reduction of 45.43%in this current. Conclusion Chrysin dilates the renal arterial ring pre-treated with 60 mmol/L KCl or 10-5 mol/L PE in a concentration-dependent fashion. Chrysin, when administered at the con-centration of the RC50, abolishes the renal arterial smooth muscle cell L-type voltage-dependent calcium channel-me-diated current and results in a non-linear up-shift of the I-V curve.