1.Lipofundin(R) MCT/LCT 20% increase left ventricular systolic pressure in an ex vivo rat heart model via increase of intracellular calcium level.
Jiyoung PARK ; Yeon A KIM ; Jeong Yeol HAN ; Sangkyu JIN ; Seong Ho OK ; Ju Tae SOHN ; Heon Keun LEE ; Young Kyun CHUNG ; Il Woo SHIN
Korean Journal of Anesthesiology 2016;69(1):57-62
BACKGROUND: Lipid emulsions have been used to treat various drug toxicities and for total parenteral nutrition therapy. Their usefulness has also been confirmed in patients with local anesthetic-induced cardiac toxicity. The purpose of this study was to measure the hemodynamic and composition effects of lipid emulsions and to elucidate the mechanism associated with changes in intracellular calcium levels in myocardiocytes. METHODS: We measured hemodynamic effects using a digital analysis system after Intralipid(R) and Lipofundin(R) MCT/LCT were infused into hearts hanging in a Langendorff perfusion system. We measured the effects of the lipid emulsions on intracellular calcium levels in H9c2 cells by confocal microscopy. RESULTS: Infusion of Lipofundin(R) MCT/LCT 20% (1 ml/kg) resulted in a significant increase in left ventricular systolic pressure compared to that after infusing modified Krebs-Henseleit solution (1 ml/kg) (P = 0.003, 95% confidence interval [CI], 2.4-12.5). Lipofundin(R) MCT/LCT 20% had a more positive inotropic effect than that of Intralipid(R) 20% (P = 0.009, 95% CI, 1.4-11.6). Both lipid emulsion treatments increased intracellular calcium levels. Lipofundin(R) MCT/LCT (0.01%) increased intracellular calcium level more than that of 0.01% Intralipid(R) (P < 0.05, 95% CI, 0.0-1.9). CONCLUSIONS: These two lipid emulsions had different inotropic effects depending on their triglyceride component. The inotropic effect of lipid emulsions could be related with intracellular calcium level.
Animals
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Blood Pressure*
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Calcium*
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Drug-Related Side Effects and Adverse Reactions
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Emulsions
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Heart*
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Hemodynamics
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Humans
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Microscopy, Confocal
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Myocardial Contraction
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Parenteral Nutrition, Total
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Perfusion
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Rats*
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Triglycerides
2.New Recorded Species in Three Genera of the Sordariomycetes in Korea.
Sangkyu PARK ; Leonid TEN ; Seung Yeol LEE ; Chang Gi BACK ; Jae Jin LEE ; Hyang Burm LEE ; Hee Young JUNG
Mycobiology 2017;45(2):64-72
In an ongoing survey of Korean indigenous fungi, three fungal strains belonging to the Sordariomycetes were isolated from soil samples. These strains were designated KNU16-001, KNU16-002, and KNU16-009, and identified as Ambrosiella grosmanniae, Acremonium sclerotigenum, and Trichocladium asperum, respectively, based on morphological characterization and phylogenetic analysis using internal transcribed spacer region sequences of ribosomal DNA. This is the first report of these species in Korea.
Acremonium
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DNA, Ribosomal
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Fungi
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Korea*
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Soil
3.Protective effect of butylated hydroxylanisole against hydrogen peroxide-induced apoptosis in primary cultured mouse hepatocytes.
Geun Hye HWANG ; Yu Jin JEON ; Ho Jae HAN ; Soo Hyun PARK ; Kyoung Min BAEK ; Woochul CHANG ; Joong Sun KIM ; Lark Kyun KIM ; You Mie LEE ; Sangkyu LEE ; Jong Sup BAE ; Jun Goo JEE ; Min Young LEE
Journal of Veterinary Science 2015;16(1):17-23
Butylated hydroxyanisole (BHA) is a synthetic phenolic compound consisting of a mixture of two isomeric organic compounds: 2-tert-butyl-4-hydroxyanisole and 3-tert-butyl-4-hydroxyanisole. We examined the effect of BHA against hydrogen peroxide (H2O2)-induced apoptosis in primary cultured mouse hepatocytes. Cell viability was significantly decreased by H2O2 in a dose-dependent manner. Additionally, H2O2 treatment increased Bax, decreased Bcl-2, and promoted PARP-1 cleavage in a dose-dependent manner. Pretreatment with BHA before exposure to H2O2 significantly attenuated the H2O2-induced decrease of cell viability. H2O2 exposure resulted in an increase of intracellular reactive oxygen species (ROS) generation that was significantly inhibited by pretreatment with BHA or N-acetyl-cysteine (NAC, an ROS scavenger). H2O2-induced decrease of cell viability was also attenuated by pretreatment with BHA and NAC. Furthermore, H2O2-induced increase of Bax, decrease of Bcl-2, and PARP-1 cleavage was also inhibited by BHA. Taken together, results of this investigation demonstrated that BHA protects primary cultured mouse hepatocytes against H2O2-induced apoptosis by inhibiting ROS generation.
Animals
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Apoptosis/*drug effects
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Butylated Hydroxyanisole/chemistry/*pharmacology
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Cell Survival/drug effects
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Cells, Cultured
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Hepatocytes/*drug effects
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Hydrogen Peroxide/*toxicity
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Male
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Mice
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Mice, Inbred ICR
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Molecular Structure