Bitar K N, Hillemeier C, Biancani P
Division of Pediatric Gastroenterology, University of Michigan Medical Center, Ann Arbor 48109-0658.
Life Sci. 1990;47(26):2429-34. doi: 10.1016/0024-3205(90)90487-c.
Substance P and bombesin induce contraction of isolated IAS smooth muscle cells by different intracellular mechanisms. The cells contracted in a dose dependent manner to both peptides. The kinetics of contraction were different. Substance P induced contraction peaked at 30 seconds and declined in a time dependent manner while bombesin induced contraction peaked at 30 seconds and was maintained for up to 8 minutes. The absence of extracellular calcium in the medium (0 calcium and 2 mM EGTA) had no affect on substance P induced contraction while it blocked bombesin induced contraction. Substance P induced contraction was blocked by the calmodulin antagonist W7 (10(-9)M) and was not affected by the PKC antagonist H7 (10(-6)M). Bombesin induced contraction was blocked by the PKC antagonist H7 and was not affected by the calmodulin antagonist W7. Our data indicate that substance P induces a transient contraction utilizing intracellular calcium and a calmodulin dependent pathway, while bombesin induces a sustained contraction utilizing calcium from extracellular sources and a calmodulin independent pathway.
P物质和蛙皮素通过不同的细胞内机制诱导离体的内括约肌平滑肌细胞收缩。细胞对这两种肽均呈剂量依赖性收缩。收缩动力学不同。P物质诱导的收缩在30秒时达到峰值,并呈时间依赖性下降,而蛙皮素诱导的收缩在30秒时达到峰值,并持续长达8分钟。培养基中无细胞外钙(0钙和2 mM乙二醇双四乙酸)对P物质诱导的收缩无影响,而阻断了蛙皮素诱导的收缩。P物质诱导的收缩被钙调蛋白拮抗剂W7(10⁻⁹M)阻断,且不受蛋白激酶C拮抗剂H7(10⁻⁶M)影响。蛙皮素诱导的收缩被蛋白激酶C拮抗剂H7阻断,且不受钙调蛋白拮抗剂W7影响。我们的数据表明,P物质利用细胞内钙和钙调蛋白依赖性途径诱导瞬时收缩,而蛙皮素利用细胞外来源的钙和钙调蛋白非依赖性途径诱导持续收缩。