Ji-Yoon Kim

Ji-Yoon Kim


Research Focus & Metrics

Academic Career Length

9Years (2018-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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20 September 2018 in Cells
Verified
Journal Article
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RSRaghavendra Baregundi Subbarao
Raghavendra Baregundi Subbarao
SOSeong-ho Ok
Seong-ho Ok
SLSoo Hee Lee
Soo Hee Lee
Dawon KangDawon Kang
Dawon Kang
EKEun-Jin Kim
Eun-Jin Kim
JSJu-Tae Sohn
Ju-Tae Sohn
This study aimed to examine the effect of lipid emulsion on the cardiotoxicity induced by doxorubicin in H9c2 rat cardiomyoblasts and elucidates the associated cellular mechanism. The effects of lipid emulsion on cell viability, Bax, cleaved caspase-8, cleaved capase-3, Bcl-XL, apoptosis, reactive oxygen species (ROS), malondialdehyde, superoxide dismutase (SOD), catalase and mitochondrial membrane potential induced by doxorubicin were examined. Treatment with doxorubicin decreased cell viability, whereas pretreatment with lipid emulsion reduced the effect of doxorubicin by increasing cell viability. Lipid emulsion also suppressed the increased expression of cleaved caspase-3, cleaved caspase-8, and Bax induced by doxorubicin. Moreover, pretreatment with lipid emulsion decreased the increased Bax/Bcl-XL ratio induced by doxorubicin. Doxorubicin-induced late apoptosis was reduced by treatment with lipid emulsion. In addition, pretreatment with lipid emulsion prior to doxorubicin enhanced glycogen synthase kinase-3β phosphorylation. The increased malondialdehyde and ROS levels by doxorubicin were reduced by lipid emulsion pretreatment. Furthermore, lipid emulsion attenuated the reduced SOD and catalase activity and the decreased mitochondrial membrane potential induced by doxorubicin. Taken together, these results suggest that lipid emulsion attenuates doxorubicin-induced late apoptosis, which appears to be associated with the inhibition of oxidative stress induced by doxorubicin.

1 November 2020 in Journal of Korean Neurosurgical Society
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Journal Article
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JKJi-Yoon Kim
Ji-Yoon Kim
IPIn Sung Park
In Sung Park
DKDong-Ho Kang
Dong-Ho Kang
YLYoung-seok Lee
Young-seok Lee
KKKyoung-Tae Kim
Kyoung-Tae Kim
SHSung Jin Hong
Sung Jin Hong
Objective : Spine surgery is associated with higher morbidity and mortality rates in elderly patients. The modified Frailty Index (mFI) is an evaluation tool to determine the frailty of an individual and how preoperative status may impact postoperative survival and outcomes. This study aimed to determine the usefulness of mFI in predicting postoperative complications in patients aged >= 75 years undergoing surgery with instrumentation. Methods : We retrospectively reviewed the perioperative course of 137 patients who underwent thoracolumbar-instrumentation spine surgery between 2011 and 2016. The preoperative risk factors were the 11 variables of the mFI, as well as body mass index (kg/cm(2)), preoperative hemoglobin, platelet, albumin, creatinine, anesthesia time, operation time, estimated blood loss, and transfusion amount. The 60-day occurrences of complication rates were used for outcome assessment. Results : Major complications after spinal instrumentation surgery occurred in 34 of 138 patients (24.6%). The mean mFI score was 0.18 +/- 0.12. When we divided patients into a pre-frail group (mFI, 0.09-0.18; n=94) and a frail group (mFI >= 0.27; n=44), only the rate of sepsis was statistically higher in the frail group than in the pre-frail group. There were significantly more major complications in patients with low albumin levels or in patients with infection or who had experienced trauma. The mFI was a more useful predictor of postoperative complications than the American Society of Anesthesiologists physical status score. Conclusion : The mFI can successfully predict postoperative morbidity and mortality in patients aged >= 75 years undergoing spine surgery. The mFI improves perioperative risk stratification that provides important information to assist in the preoperative counselling of patients and their families.

1 January 2021 in Korean Journal of Neurotrauma
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Journal Article
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TATae Yong An
Tae Yong An
JKJi-Yoon Kim
Ji-Yoon Kim
YLYoung-seok Lee
Young-seok Lee
An TY, et al. Korean J Neurotrauma. 2021 Sep;17:e23. https://doi.org/10.13004/kjnt.2021.17.e23

1 January 2019 in Korean Journal of Neurotrauma
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JKJonggil Kim
Jonggil Kim
JKJi-Yoon Kim
Ji-Yoon Kim
JLJa Myoung Lee
Ja Myoung Lee
DKDong Ho Kang
Dong Ho Kang
CLChul-Hee HEE Lee
Chul-Hee HEE Lee
YLYoung-seok Lee
Young-seok Lee
Kim J, et al. Korean J Neurotrauma. 2019 Jul;15:e24. https://doi.org/10.13004/kjnt.2019.15.e24

1 November 2021 in Archives of Plastic Surgery
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Journal Article
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YKYun Hyun Kim
Yun Hyun Kim
JRJeong Yeop Ryu
Jeong Yeop Ryu
JLJoon Seok Lee
Joon Seok Lee
SLSeok Jong Lee
Seok Jong Lee
JLJong Min Lee
Jong Min Lee
HCHo Yun Chung
Ho Yun Chung
Background Venous malformations (VMs) are the most common type of vascular malformations. Intramuscular venous malformations (IMVMs) are lesions involving the muscles, excluding intramuscular hemangiomas. The purpose of this study was to compare clinical outcomes between patients with IMVMs who were treated with sclerotherapy and those who were treated with surgical excision. Methods Of 492 patients with VMs treated between July 2011 and August 2020 at a single medical center for vascular anomalies, 63 patients diagnosed with IMVM were retrospectively reviewed. Pain, movement limitations, swelling, and quality of life (QOL) were evaluated subjectively, while radiological outcomes were assessed by qualified radiologists at the center. Complication rates were also evaluated, and radiological and clinical examinations were used to determine which treatment group (sclerotherapy or surgical excision) exhibited greater improvement. Results Although there were no significant differences in pain (P=0.471), swelling (P=0.322), or the occurrence of complications (P=0.206) between the two treatment groups, the surgical treatment group exhibited significantly better outcomes with regard to movement limitations (P=0.010), QOL (P=0.013), and radiological outcomes (P=0.017). Moreover, both duplex ultrasonography and magnetic resonance imaging showed greater improvements in clinical outcomes in the surgical excision group than in the sclerotherapy group. Conclusions Although several studies have examined IMVM treatment methods, no clear guidelines for treatment selection have been developed. Based on the results of this study, surgical excision is strongly encouraged for the treatment of IMVMs.

Verified
Journal Article
Open access
PDF file
SLSoo Hee Lee
Soo Hee Lee
Dawon KangDawon Kang
Dawon Kang
SOSeong-ho Ok
Seong-ho Ok
SKSeong-Chun Kwon
Seong-Chun Kwon
HKHyun-Jin Kim
Hyun-Jin Kim
JSJu-Tae Sohn
Ju-Tae Sohn
The goal of this study was to investigate the effect of lipid emulsion on a toxic dose of local anesthetic-mediated reduction of vasodilation evoked by the ATP-sensitive potassium (KATP) channel agonist levcromakalim. The effect of lipid emulsion (LE) and linoleic acid on the local anesthetic-mediated reduction of vasodilation and membrane hyperpolarization evoked by levcromakalim was assessed in isolated endothelium-denuded vessels (rat aorta and mesenteric artery) and aortic vascular smooth muscle cells. The effect of LE and linoleic acid on KATP channel activity in transfected HEK-293 cells was investigated, as was the effect of LE on bupivacaine concentration. The efficacy of LE in attenuating the local anesthetic-mediated reduction of vasodilation evoked by levcromakalim was correlated with the lipid solubility of the local anesthetic. Linoleic acid attenuated the bupivacaine-mediated reduction of vasodilation evoked by levcromakalim. LE decreased the bupivacaine-mediated reduction of membrane hyperpolarization evoked by levcromakalim but did not significantly alter the mepivacaine-mediated reduction. LE and linoleic acid both reversed the bupivacaine-mediated decrease of KATP activity and enhanced KATP activity. LE decreased the bupivacaine concentration. Linoleic acid may be the major contributor to LE-induced attenuation of bupivacaine-mediated reduction of vasodilation evoked by levcromakalim via the direct activation of KATP channels and indirect effects.