• 한국생물물리학회:학술대회논문집
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• 한국생물물리학회 1996년도 정기총회 및 학술발표회
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• pp.5-5
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• 1996

In sino-atrial node cells which act as the normal pacemaker of the heart, K conductance in resting state is minimal due to the absence of inward rectifier K channels K conductance only increases when the membrane is depolarized by the activation of the delayed rectifier K current I$\_$k/. In the present study, we investigated the gating mechanism of$\_$k/ using the whole cell patch clamp technique in isolated single sinoatrial cells of the rabbit. (omitted)

• 한국생물물리학회:학술대회논문집
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• 한국생물물리학회 1996년도 정기총회 및 학술발표회
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• pp.42-42
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• 1996

Adrenal chromaffin cells secrete catecholamine in response to acetylcholine. The secretory response has absolute requirement for extracellular calcium, indicating that $Ca^{2+}$ influx through voltage operated $Ca^{2+}$ channels (VOCC) is the primary trigger of the secretion cascade. Although the existence of various types of $Ca^{2+}$ channels has been explore using patch clamp techique in adrenal chromaffin cells, the contribution of different types of $Ca^{2+}$ channels to catecholamine secretion remains to be establised. (omitted)omitted)

• 대한전기학회:학술대회논문집
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• 대한전기학회 1996년도 하계학술대회 논문집 B
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• pp.841-843
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• 1996

This paper presents efficient protection countermeasure against lightning and surge for the control & instrumentation equipment using TVSS(transient voltage surge suppressor) and TEC(transient earth clamp). We propose the zone protection technique with TVSS and the use of TEC for clearing potential difference between frame ground and signal ground.

• 대한전기학회:학술대회논문집
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• 대한전기학회 2005년도 제36회 하계학술대회 논문집 B
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• pp.1398-1400
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• 2005

In this paper, a modular dc-to-dc converter, in order to apply to the control board of train vehicles, is presented. Forward converter with active-clamp reset circuit and synchronous rectifier(SR) is employed to achieve high efficiency. To reduce the size and height of the converter, low profile magnetic components are used. The design and performance of the modular dc-to-dc converter with experiments on a 50W(5V/10A) prototype for the 60V$\sim$140V input voltage range are presented.

• 전력전자학회:학술대회논문집
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• 전력전자학회 2010년도 추계학술대회
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• pp.190-191
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• 2010

In this paper, an analysis for leakage inductance of transformer in active clamped flyback inverter is presented. In the active clamp circuit of flyback inverter, the leakage inductance influences on the voltage across the primary switch and the resonant capacitor. Therefore, it is essential to optimize the leakage inductance design. In order to verify the theoretical analysis for the leakage inductance, PSIM simulation is used.

• 한국생물물리학회:학술대회논문집
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• 한국생물물리학회 1997년도 학술발표회
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• pp.26-26
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• 1997

In the present study, we recorded CCh-activated nonselective cation (NSC) current in guinea-pig gastric smooth muscle cells and investigated the characteristics of the current. In whole-cell voltage-clamp mode, CCh activated NSC current. The same NSC current could be activated by internal dialysis of GTP${\gamma}$S.(omitted)

• 전력전자학회:학술대회논문집
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• 전력전자학회 2018년도 추계학술대회
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• pp.223-224
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• 2018

본 논문에서는 전기자동차용 저전압 배터리 충전기(Low-voltage DC-DC Converter, LDC)에 적합한 입력 직렬-출력 병렬 구조의 능동 클램프 포워드 컨버터의 모델링 및 제어기 설계를 제안한다. 제안하는 컨버터는 모든 스위치에서 소프트 스위칭을 성취하기 때문에 높은 효율을 달성할 수 있다. 또한 누설 인덕턴스의 영향을 포함한 컨버터의 정확한 소신호 모델을 통하여 모델링 기반의 제어기 설계를 제시한다. 제어기의 시뮬레이션 및 3.2kW급 시작품의 실험을 통하여 제안하는 컨버터의 성능을 검증하였다.

• 대한약학회:학술대회논문집
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• 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2-2
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• pp.178.3-178.3
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• 2003

P2X receptors are ligand gated cation channels activated by the binding of extracellular adenosine 5'-triphosphate (ATP) and classified into 7 subtype families. $P2X_1$ receptors are abundantly expressed in smooth muscle mediates blood vessel and mediate constriction upon binding of neuronal ATP. The activation of $P2X_3$ receptor by ATP has been known to initiate the pain signaling in the peripheral nervous system, which is involved in chronic inflammatory nociception and neuropathic pain by nerve injury. (omitted)

• The Korean Journal of Physiology
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• 제27권2호
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• pp.139-150
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• 1993

We have reported that dopamine potentiates spontaneous contractions dose-dependently in guinea-pig antral circular muscle strips (Hwang et al, 1991). To clarify the underlying excitatory mechanism of dopamine on the gastric smooth muscle, the effects of dopamine on voltage-dependent $Ca^{2+}\;currents\;and\;Ca^{2+}\;-dependent\;K^+\;currents$ were observed in enzymatically dispersed guinea-pig gastric myocytes using the whole-cell voltage-clamp technique. Experiments were also done using isometric tension recording and conventional intracellular microelectrode techniques. 1) The effect of dopamine on the spontaneous contraction of antral circular muscle strips of the guinea-pig was excitatory in a dose-dependent manner, and was blocked by phentolamine, an ${\alpha}-adrenoceptor$ blocker. 2) The slow waves were not changed by dopamine. 3) The voltage-operated inward $Ca^{2+}$ current was not influenced by dopamine. 4) The $Ca^{2+}\;-dependent\;K^+$ outward current, which might reflect the changes of intracellular calcium concentration, was enhanced by dopamine. This effect was abolished by phentolamine. 5) The enhancing effect of dopamine on the $Ca^{2+}\;-dependent\;K^+$ current disappeared with heparin which is known to block the action of $InsP_3$. From these results, it is suggested that dopamine acts via $InsP_3-mediated\;Ca^{2+}$ mobilization from intracellular stores and such action potentiates the spontaneous contraction of guinea-pig gastric smooth muscle.

• The Korean Journal of Physiology and Pharmacology
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• 제21권2호
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• pp.225-232
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• 2017

We demonstrated the effect of nortriptyline, a tricyclic antidepressant drug and serotonin reuptake inhibitor, on voltage-dependent $K^+$ (Kv) channels in freshly isolated rabbit coronary arterial smooth muscle cells using a whole-cell patch clamp technique. Nortriptyline inhibited Kv currents in a concentration-dependent manner, with an apparent $IC_{50}$ value of $2.86{\pm}0.52{\mu}M$ and a Hill coefficient of $0.77{\pm}0.1$. Although application of nortriptyline did not change the activation curve, nortriptyline shifted the inactivation current toward a more negative potential. Application of train pulses (1 or 2 Hz) did not change the nortriptyline-induced Kv channel inhibition, suggesting that the effects of nortiprtyline were not use-dependent. Preincubation with the Kv1.5 and Kv2.1/2.2 inhibitors, DPO-1 and guangxitoxin did not affect nortriptyline inhibition of Kv channels. From these results, we concluded that nortriptyline inhibited Kv channels in a concentration-dependent and state-independent manner independently of serotonin reuptake.