Department of Pharmacology, Faculty of Medicine, Saga University, Nabeshima, Saga, Japan; Department of Cell Physiology, Nagoya City University Medical School, Mizuho-ku, Nagoya, Japan; and
Department of Cell Physiology, Nagoya City University Medical School, Mizuho-ku, Nagoya, Japan; and.
Am J Physiol Gastrointest Liver Physiol. 2015 Mar 1;308(5):G378-88. doi: 10.1152/ajpgi.00308.2014. Epub 2014 Dec 24.
Slow waves (slow wavesICC) were recorded from myenteric interstitial cells of Cajal (ICC-MY) in situ in the rabbit small intestine, and their properties were compared with those of mouse small intestine. Rabbit slow wavesICC consisted of an upstroke depolarization followed by a distinct plateau component. Ni(2+) and nominally Ca(2+)-free solutions reduced the rate-of-rise and amplitude of the upstroke depolarization. Replacement of Ca(2+) with Sr(2+) enhanced the upstroke component but decreased the plateau component of rabbit slow wavesICC. In contrast, replacing Ca(2+) with Sr(2+) decreased both components of mouse slow wavesICC. The plateau component of rabbit slow wavesICC was inhibited in low-extracellular-Cl(-)-concentration (low-[Cl(-)]o) solutions and by 4,4'-diisothiocyanostilbene-2,2'-disulfonic acid (DIDS), an inhibitor of Cl(-) channels, cyclopiazonic acid (CPA), an inhibitor of internal Ca(2+) pumps, or bumetanide, an inhibitor of Na(+)-K(+)-2Cl(-) cotransporter (NKCC1). Bumetanide also inhibited the plateau component of mouse slow wavesICC. NKCC1-like immunoreactivity was observed mainly in ICC-MY in the rabbit small intestine. Membrane depolarization with a high-K(+) solution reduced the upstroke component of rabbit slow wavesICC. In cells depolarized with elevated external K(+), DIDS, CPA, and bumetanide blocked slow wavesICC. These results suggest that the upstroke component of rabbit slow wavesICC is partially mediated by voltage-dependent Ca(2+) influx, whereas the plateau component is dependent on Ca(2+)-activated Cl(-) efflux. NKCC1 is likely to be responsible for Cl(-) accumulation in ICC-MY. The results also suggest that the mechanism of the upstroke component differs in rabbit and mouse slow wavesICC in the small intestine.
从兔小肠的肠肌间神经丛 Cajal 间质细胞(ICC-MY)原位记录到慢波(慢波 ICC),并将其特性与小鼠小肠的慢波进行比较。兔慢波 ICC 由上升去极化 followed 一个明显的平台组成。Ni(2+)和名义上的无钙溶液减少了上升去极化的上升速率和幅度。用 Sr(2+)代替 Ca(2+)增强了兔慢波 ICC 的上升成分,但降低了平台成分。相比之下,用 Sr(2+)代替 Ca(2+)降低了小鼠慢波 ICC 的两个成分。低细胞外 Cl(-)浓度(低-[Cl(-)]o)溶液和 4,4'-二异硫氰基二苯乙烯-2,2'-二磺酸(DIDS),一种 Cl(-)通道抑制剂,环匹阿尼酸(CPA),一种内部 Ca(2+)泵抑制剂,或布美他尼,一种 Na(+)-K(+)-2Cl(-)共转运体(NKCC1)抑制剂,抑制兔慢波 ICC 的平台成分。布美他尼也抑制了小鼠慢波 ICC 的平台成分。NKCC1 样免疫反应性主要在兔小肠的 ICC-MY 中观察到。高钾溶液引起的膜去极化降低了兔慢波 ICC 的上升成分。在高钾溶液去极化的细胞中,DIDS、CPA 和布美他尼阻断了慢波 ICC。这些结果表明,兔慢波 ICC 的上升成分部分由电压依赖性 Ca(2+)内流介导,而平台成分依赖于 Ca(2+)激活的 Cl(-)外排。NKCC1 可能负责 ICC-MY 中的 Cl(-)积累。这些结果还表明,在小肠中,兔和小鼠慢波 ICC 的上升成分机制不同。