1.Effects of ATP on Pacemaker Activity of Interstitial Cells of Cajal from the Mouse Small Intestine
Il Koo PARK ; Jin Ho KIM ; Chan Guk PARK ; Man Yoo KIM ; Shankar Prasad PARAJULI ; Chan Sik HONG ; Seok CHOI ; Jae Yeoul JUN
Chonnam Medical Journal 2018;54(1):63-71
Purinergic receptors play an important role in regulating gastrointestinal (GI) motility. Interstitial cells of Cajal (ICCs) are pacemaker cells that regulate GI smooth muscle activity. We studied the functional roles of external adenosine 5′-triphosphate (ATP) on pacemaker activity in cultured ICCs from mouse small intestines by using the whole-cell patch clamp technique and intracellular Ca²⁺ ([Ca²⁺]ᵢ) imaging. External ATP dose-dependently depolarized the resting membrane and produced tonic inward pacemaker currents, and these effects were antagonized by suramin, a purinergic P2 receptor antagonist. ATP-induced effects on pacemaker currents were suppressed by an external Na⁺-free solution and inhibited by the nonselective cation channel blockers, flufenamic acid and niflumic acid. The removal of external Ca²⁺ or treatment with thapsigargin (inhibitor of Ca²⁺ uptake into endoplasmic reticulum) inhibited the ATP-induced effects on pacemaker currents. Spontaneous [Ca²⁺]ᵢ oscillations were enhanced by external ATP. These results suggest that external ATP modulates pacemaker activity by activating nonselective cation channels via external Ca²⁺ influx and [Ca²⁺]ᵢ release from the endoplasmic reticulum. Thus, it seems that activating the purinergic P2 receptor may modulate GI motility by acting on ICCs in the small intestine.
Adenosine
;
Adenosine Triphosphate
;
Animals
;
Endoplasmic Reticulum
;
Flufenamic Acid
;
Interstitial Cells of Cajal
;
Intestine, Small
;
Membranes
;
Mice
;
Muscle, Smooth
;
Niflumic Acid
;
Pacemaker, Artificial
;
Receptors, Purinergic
;
Receptors, Purinergic P2
;
Suramin
;
Thapsigargin
2.The mechanism of t-butylhydroperoxide-induced apoptosis in IMR-32 human neuroblastoma cells.
Jung Ae KIM ; Yong Soo LEE ; Keun HUH
The Korean Journal of Physiology and Pharmacology 1999;3(1):19-28
Apoptosis has been implicated in the pathophysiological mechanisms of various neurodegenerative diseases. In a variety of cell types, oxidative stress has been demonstrated to play an important role in the apoptotic cell death. However, the exact mechanism of oxidative stress-induced apoptosis in neuronal cells is not known. In this study, we induced oxidative stress in IMR-32 human neuroblastoma cells with tert-butylhydroperoxide (TBHP), which was confirmed by significantly reduced glutathione content and glutathione reductase activity, and increased glutathione peroxidase activity. TBHP induced decrease in cell viability and increase in DNA fragmentation, a hallmark of apoptosis, in a dose-dependent manner. TBHP also induced a sustained increase in intracellular Ca2+ concentration, which was completely prevented either by EGTA, an extracellular Ca2+ chelator or by flufenamic acid (FA), a non-selective cation channel (NSCC) blocker. These results indicate that the TBHP-induced intracellular Ca2+ increase may be due to Ca2+ influx through the activation of NSCCs. In addition, treatment with either an intracellular Ca2+ chelator (BAPTA/AM) or FA significantly suppressed the TBHP-induced apoptosis. Moreover, TBHP increased the expression of p53 gene but decreased c-myc gene expression. Taken together, these results suggest that the oxidative stress-induced apoptosis in neuronal cells may be mediated through the activation of intracellular Ca2+ signals and altered expression of p53 and c-myc.
Apoptosis*
;
Cell Death
;
Cell Survival
;
DNA Fragmentation
;
Egtazic Acid
;
Flufenamic Acid
;
Genes, myc
;
Genes, p53
;
Glutathione
;
Glutathione Peroxidase
;
Glutathione Reductase
;
Humans*
;
Neuroblastoma*
;
Neurodegenerative Diseases
;
Neurons
;
Oxidative Stress
;
tert-Butylhydroperoxide