Luo Ya-Li, Zeng Jun-Wei, Yu Mei, Wei Yu-Ling, Qu Song-Yi, Li Wei, Zheng Tian-Zhen
Department of Physiology, Lanzhou Medical College, Lanzhou 730000, Gansu Province, China.
World J Gastroenterol. 2005 Feb 14;11(6):863-6. doi: 10.3748/wjg.v11.i6.863.
To investigate the effect of rhubarb on contractile response of isolated gallbladder muscle strips from guinea pigs and its mechanism.
Guinea pigs were killed to remove the whole gallbladder. Two or three smooth muscle strips (8 mm x 3 mm) were cut along the longitudinal direction. The mucosa on each strip was carefully removed. Each longitudinal muscle strip was suspended in a tissue chamber containing 5 mL Krebs solution (37 degrees), bubbled continuously with 950 mL/L O(2) and 50 mL/L CO(2). The resting tension (g), mean contractile amplitude (mm), and contractile frequency (waves/min) were simultaneously recorded on recorders. After 2-h equilibration, rhubarb (10, 20, 70, 200, 700, 1,000 g/L) was added cumulatively to the tissue chamber in turns every 2 min to observe their effects on gallbladder. Antagonists were given 3 min before administration of rhubarb to investigate the possible mechanism.
Rhubarb increased the resting tension (from 0 to 0.40+/-0.02, P<0.001), and decreased the mean contractile amplitude (from 5.22+/-0.71 to 2.73+/-0.41, P<0.001). It also increased the contractile frequency of the gallbladder muscle strips in guinea pigs (from 4.09+/-0.46 to 6.08+/-0.35, P<0.001). The stimulation of rhubarb on the resting tension decreased from 3.98+/-0.22 to 1.58+/-0.12 by atropine (P<0.001), from 3.98+/-0.22 to 2.09+/-0.19 by verapamil (P<0.001) and from 3.98+/-0.22 to 2.67+/-0.43 by phentolamine (P<0.005). But the effect was not inhibited by hexamethonium (P>0.05). In addition, the action of mean amplitude and frequency was not inhibited by the above antagonists.
Rhubarb can stimulate the motility of isolated gallbladder muscle strips from guinea pigs. The stimulation of rhubarb might be relevant with M receptor, Ca(2+) channel and alpha receptor partly.
研究大黄对豚鼠离体胆囊肌条收缩反应的影响及其机制。
处死豚鼠,取出完整胆囊。沿纵向切取两三条平滑肌条(8mm×3mm)。仔细去除每条肌条上的黏膜。将每条纵行肌条悬挂于含5mL Krebs液(37℃)的组织浴槽中,持续通入950mL/L O₂和50mL/L CO₂。在记录仪上同步记录静息张力(g)、平均收缩幅度(mm)和收缩频率(次/分钟)。平衡2小时后,每隔2分钟依次向组织浴槽中累积加入大黄(10、20、70、200、700、1000g/L),观察其对胆囊的作用。在给予大黄前3分钟给予拮抗剂,以研究可能的机制。
大黄增加了静息张力(从0增至0.40±0.02,P<0.001),降低了平均收缩幅度(从5.22±0.71降至2.73±0.41,P<0.001)。它还增加了豚鼠胆囊肌条的收缩频率(从4.09±0.46增至6.08±0.35,P<0.001)。大黄对静息张力的刺激作用经阿托品后从3.98±0.22降至1.58±0.12(P<0.001),经维拉帕米后从3.98±0.22降至2.09±0.19(P<0.001),经酚妥拉明后从3.98±0.22降至2.67±0.43(P<0.005)。但六甲铵对此作用无抑制作用(P>0.05)。此外,上述拮抗剂对平均幅度和频率的作用无抑制作用。
大黄可刺激豚鼠离体胆囊肌条的运动。大黄的刺激作用可能部分与M受体、Ca²⁺通道和α受体有关。