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Rho激酶和蛋白激酶C参与β-七叶皂苷处理的大鼠和豚鼠膀胱中卡巴胆碱诱导的钙敏化作用。

Involvement of Rho kinase and protein kinase C in carbachol-induced calcium sensitization in beta-escin skinned rat and guinea-pig bladders.

作者信息

Durlu-Kandilci N Tugba, Brading Alison F

机构信息

Hacettepe University, Faculty of Pharmacy, Department of Pharmacology, 06100, Sihhiye, Ankara, Turkey.

出版信息

Br J Pharmacol. 2006 Jun;148(3):376-84. doi: 10.1038/sj.bjp.0706723.

Abstract
  1. The signal transduction pathways involved in carbachol (CCh)-induced calcium sensitization in beta-escin permeabilized rat and guinea-pig bladder smooth muscles were investigated and the results were compared with guinea-pig taenia caecum. 2. Calcium contractions elicited cumulatively (pCa 7.5-5) in the presence of calmodulin were significantly increased in all three tissues when CCh (50 microM) was added to the medium. 3. Under constant [Ca2+]i conditions (pCa 6), calmodulin (1 microM) and then GTP (100 microM) initiated significant contractions. CCh (50 microM) added to the bath caused a further contraction in all three tissues - calcium sensitization. This sensitization was significantly inhibited by atropine (50 microM). 4. The incubation of the tissues with the IP3-receptor blocker 2-APB (30 microM) reduced the subsequent development of calcium sensitization by CCh in rat bladder but did not affect it in guinea-pig bladder and taenia ceacum. 5. The Rho kinase (ROK) inhibitor Y-27632 (5 microM) added in the presence of CCh reversed the calcium sensitization in rat bladder, whereas a transient contraction followed by a relaxation to a level not significantly different from the CCh contraction was seen in both guinea-pig bladder and taenia caecum. Y-27632 (1 microM) continuously present significantly inhibited the CCh-induced Ca2+ sensitization in rat bladder but not in guinea-pig bladder or taenia caecum. 6. In the presence of cyclopiazonic acid (CPA) (1 microM) and calmodulin (1 microM), Y-27632 (5 microM) did not change the calcium response curve (3 x 10(-7)-10(-5) M) in rat bladder but increased the contractile responses significantly in both guinea-pig bladder and taenia caecum. 7. The protein kinase C (PKC) inhibitor GF 109203X (5 microM) added in the presence of CCh inhibited the calcium sensitization induced by this muscarinic agonist in all three tissues in different ratios. 8. In conclusion, muscarinic receptor activation induces calcium sensitization in rat and guinea-pig detrusor smooth muscles but there are differences in their pathways.
摘要
  1. 研究了卡巴胆碱(CCh)诱导的β-七叶皂苷通透化大鼠和豚鼠膀胱平滑肌钙敏化所涉及的信号转导途径,并将结果与豚鼠盲肠带进行了比较。2. 在钙调蛋白存在的情况下,累积引发的钙收缩(pCa 7.5 - 5)在向培养基中添加CCh(50 μM)时,所有三种组织中均显著增加。3. 在恒定的[Ca2+]i条件下(pCa 6),钙调蛋白(1 μM)然后是GTP(100 μM)引发显著收缩。向浴槽中添加CCh(50 μM)在所有三种组织中引起进一步收缩——钙敏化。这种敏化被阿托品(50 μM)显著抑制。4. 用IP3受体阻滞剂2-APB(30 μM)孵育组织可降低CCh在大鼠膀胱中随后的钙敏化发展,但对豚鼠膀胱和盲肠带无影响。5. 在CCh存在下添加Rho激酶(ROK)抑制剂Y-27632(5 μM)可逆转大鼠膀胱中的钙敏化,而在豚鼠膀胱和盲肠带中均观察到短暂收缩后松弛至与CCh收缩无显著差异的水平。持续存在的Y-27632(1 μM)显著抑制大鼠膀胱中CCh诱导的Ca2+敏化,但对豚鼠膀胱或盲肠带无抑制作用。6. 在环匹阿尼酸(CPA)(1 μM)和钙调蛋白(1 μM)存在的情况下,Y-27632(5 μM)在大鼠膀胱中未改变钙反应曲线(3×10(-7)-10(-5) M),但在豚鼠膀胱和盲肠带中显著增加了收缩反应。7. 在CCh存在下添加蛋白激酶C(PKC)抑制剂GF 109203X(5 μM)以不同比例抑制了这种毒蕈碱激动剂在所有三种组织中诱导的钙敏化。8. 总之,毒蕈碱受体激活在大鼠和豚鼠逼尿肌平滑肌中诱导钙敏化,但它们的途径存在差异。

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