Takeda K, Torikai S, Asano Y, Imai M
Kidney Int. 1986 Apr;29(4):863-9. doi: 10.1038/ki.1986.78.
In order to know the role of cytosolic calcium in the modulation of the hormone action on sodium chloride transport across the thick ascending limbs of Henle's loop, we examined whether verapamil, a blocker of cellular calcium entry, can modulate the effects of arginine vasopressin (AVP) or glucagon in stimulating transepithelial voltage (Vt) and cyclic AMP generation in the mouse medullary thick ascending limb (MAL). The pretreatment of the renal tubule with 5 X 10(-5)M verapamil reduced the Vt stimulated with 200 microU/mliter AVP from 1.7 +/- 0.3 mV to 0.4 +/- 0.4 mV (N = 7, P less than 0.05). The changes in Vt were well correlated with those of unidirectional Cl flux from the lumen to the bath. However, verapamil did not influence the Vt stimulated with 10(-3) M dibutyryl cyclic AMP. The pretreatment of the MAL with 10(-5) M verapamil also inhibited the cyclic AMP generation in the MAL from 72.1 +/- 17.9 to 50.6 +/- 13.6 fmoles/mm/7 min (N = 7, P less than 0.05) as well as in the medullary collecting tubule from 147.6 +/- 46.6 to 121.2 +/- 41.6 fmoles/mm/7 min (N = 4, P less than 0.05). The effect of verapamil in inhibiting the AVP-stimulated cAMP was dose-dependent: the cAMP generation was inhibited by 28.9 +/- 6.8 and 61.1 +/- 9.3% with 10(-5) M and 10(-4) M verapamil, respectively. When verapamil was added to the medium simultaneously with AVP, the generation of cyclic AMP was unaffected.(ABSTRACT TRUNCATED AT 250 WORDS)
为了了解胞质钙在激素对氯化钠经髓袢升支粗段转运作用调节中的作用,我们研究了细胞钙内流阻滞剂维拉帕米是否能调节精氨酸加压素(AVP)或胰高血糖素对小鼠髓质升支粗段(MAL)跨上皮电压(Vt)和环磷酸腺苷(cAMP)生成的刺激作用。用5×10⁻⁵M维拉帕米预处理肾小管,可使200微单位/毫升AVP刺激的Vt从1.7±0.3毫伏降至0.4±0.4毫伏(N = 7,P<0.05)。Vt的变化与从管腔到浴液的单向氯通量变化密切相关。然而,维拉帕米并不影响10⁻³M二丁酰环磷酸腺苷刺激的Vt。用10⁻⁵M维拉帕米预处理MAL,也可使MAL中的cAMP生成从72.1±