Skip Navigation
Skip to contents

대한신장학회


간행물 검색

현재 페이지 경로
  • HOME
  • 간행물
  • 간행물 검색
논문분류 춘계학술대회 초록집
제목 The role of L-type Calcium Channels in ureter smooth muscle action potential and its modulation by Nifedipine
저자 Chitaranjan Mahapatra, Rohit Manchanda
출판정보 2019; 2019(1):
키워드 Ureter Smooth Muscle | Action Potential | L -type calcium channel | Nifedipine
초록 Adequate abnormalities to kidney and upper urinary tract are strongly associated with renal failure. Abnormal peristaltic contraction of the ureter smooth muscle (USM) causes pathophysiological condition to the urinary system. It is demonstrated that the USM contractions are discretely initiated by the USM cell action potentials (APs). L- type calcium channels (LTCCs) are prevalent in different systems and hold immense importance for maintaining/performing selective functions.  The present study investigates the role of LTCCs in modulating the USM cell APs. The USM cell is described as an equivalent electrical circuit with a number of variable conductances representing two voltage-gated Ca2+ (T - type and L- type) channels, one voltage-gated fast potassium channels, one calcium-dependent large conductance potassium channels, and HCN channel. A drug model for the LTCC blocker nifedipine is simulated by multiplying the maximal conductance of LTCC with a scaling factor between 0 and 1 to mimic the drug concentration. The resting membrane potential (RMP) of the USM is set at ─52mV. The peak amplitude of the AP and total inward current are substantially reduced after adding nifedipine by 50% (black solid line) and 100% (blue solid line) of its control value (red solid line) in Figure 1.  The results show that LTCC plays important role in generating APs and it is the major contributor to the total inward current.  The experimental USM cell APs show a large variation in terms of AP duration. It is also observed that the inactivation time constant of the L –type Ca2+ channels regulate the repolarization phase and duration of the AP. The L-type Ca2+ channel blocker can be used as a new pharmacological target for abnormal ureter contraction. The other specific roles L-type Ca2+ channel in cellular signaling can also be investigated by future studies.
원문(PDF) PDF 원문보기
위로가기