1.Development of S-Methylmethionine Sulfonium Derivatives and Their Skin-Protective Effect against Ultraviolet Exposure.
Won Serk KIM ; Wang Kyun KIM ; Nahyun CHOI ; Wonhee SUH ; Jinu LEE ; Dae Duk KIM ; Ikyon KIM ; Jong Hyuk SUNG
Biomolecules & Therapeutics 2018;26(3):306-312
In a previous study, we have demonstrated that S-methylmethionine sulfonium (SMMS) confers wound-healing and photoprotective effects on the skin, suggesting that SMMS can be used as a cosmetic raw material. However, it has an unpleasant odor. Therefore, in the present study, we synthesized odor-free SMMS derivatives by eliminating dimethyl sulfide, which is the cause of the unpleasant odor and identified two derivatives that exhibited skin-protective effects: one derivative comprised (2S,4S)- and (2R,4S)-2-phenylthiazolidine-4-carboxylic acid and the other comprised (2S,4R)-, (2S,4S)-, (2R,4R)-, and (2R,4S)-2-phenyl-1,3-thiazinane-4-carboxylic acid. We performed in vitro proliferation assays using human dermal fibroblasts (hDFs) and an immortalized human keratinocyte cell line (HaCaT). The two SMMS derivatives were shown to increase hDF and HaCaT cell proliferation as well as improve their survival by protecting against ultraviolet exposure. Moreover, the derivatives regulated the expression of collagen type I and MMP mRNAs against ultraviolet exposure in hDFs, suggesting that these derivatives can be developed as cosmetic raw materials.
Cell Line
;
Cell Proliferation
;
Collagen Type I
;
Fibroblasts
;
Humans
;
In Vitro Techniques
;
Keratinocytes
;
Odors
;
Reactive Oxygen Species
;
RNA, Messenger
;
Skin
;
Vitamin U*
2.Evaluation of clinical outcomes of implants placed into the maxillary sinus with a perforated sinus membrane: a retrospective study.
Gwang Seok KIM ; Jae Wang LEE ; Jong Hyon CHONG ; Jeong Joon HAN ; Seunggon JUNG ; Min Suk KOOK ; Hong Ju PARK ; Sun Youl RYU ; Hee Kyun OH
Maxillofacial Plastic and Reconstructive Surgery 2016;38(12):50-
BACKGROUND: The aim of this study was to evaluate the clinical outcomes of implants that were placed within the maxillary sinus that has a perforated sinus membrane by the lateral window approach. METHODS: We examined the medical records of the patients who had implants placed within the maxillary sinus that has a perforated sinus membrane by the lateral approach at the Department of Oral and Maxillofacial Surgery of Chonnam National University Dental Hospital from January 2009 to December 2015. There were 41 patients (male:female = 28:13). The mean age of patients was 57.2 ± 7.2 years at the time of operation (range, 20–76 years). The mean follow-up duration was 2.1 years (range, 0.5–5 years) after implant placement. Regarding the method of sinus elevation, only the lateral approach was included in this study. RESULTS: Ninety-nine implants were placed in 41 patients whose sinus membranes were perforated during lateral approach. The perforated sinus membranes were repaired with a resorbable collagen membrane. Simultaneous implant placements with sinus bone grafting were performed in 37 patients, whereas delayed placements were done in four patients. The average residual bone height was 3.4 ± 2.0 mm in cases of simultaneous implant placement and 0.6 ± 0.9 mm in cases of delayed placement. Maxillary bone graft with implant placement, performed on the patients with a perforated maxillary sinus membrane did not fail, and the cumulative implant survival rate was 100%. CONCLUSIONS: In patients with perforations of the sinus mucosa, sinus elevation and implant placement are possible regardless of the location and size of membrane perforation. Repair using resorbable collagen membrane is a predictable and reliable technique.
Bone Transplantation
;
Collagen
;
Follow-Up Studies
;
Humans
;
Jeollanam-do
;
Maxilla
;
Maxillary Sinus*
;
Medical Records
;
Membranes*
;
Methods
;
Mucous Membrane
;
Retrospective Studies*
;
Surgery, Oral
;
Survival Rate
;
Transplants
3.Retrospective clinical study of an implant with a sandblasted, large-grit, acid-etched surface and internal connection: analysis of short-term success rate and marginal bone loss.
Jae Wang LEE ; Jun Hyeong AN ; Sang Hoon PARK ; Jong Hyon CHONG ; Gwang Seok KIM ; JeongJoon HAN ; Seunggon JUNG ; Min Suk KOOK ; Hee Kyun OH ; Sun Youl RYU ; Hong Ju PARK
Maxillofacial Plastic and Reconstructive Surgery 2016;38(11):42-
BACKGROUND: The purpose of this retrospective study was to evaluate the clinical utility of an implant with a sandblasted, large-grit, acid-etched (SLA) surface and internal connection. METHODS: Six patients who received dental implants in the Department of Oral and Maxillofacial Surgery, Chonnam National University Dental Hospital, were analyzed by factors influencing the success rate and marginal bone loss. Factors included patient’s age, sex, implant installation site, whether bone graft was done, type of bone graft materials, approaching method if sinus lift was done, and the size of the fixture. In addition, the marginal bone loss was analyzed by using a radiograph. RESULTS: All implants were successful, and the cumulative survival rate was 100 %. Average marginal bone loss of 6 months after the installation was 0.52 mm and 20 months after the functional loading was 1.06 mm. Total marginal bone resorption was 1.58 mm on average. There was no statistically significant difference in mesial and distal marginal bone loss. CONCLUSIONS: The short-term clinical success rate of the implant with an SLA surface and internal connection was satisfactory. Moreover, the marginal bone loss was also consistent with the implant success criteria.
Bone Resorption
;
Clinical Study*
;
Dental Implants
;
Humans
;
Jeollanam-do
;
Methods
;
Retrospective Studies*
;
Surgery, Oral
;
Survival Rate
;
Transplants
4.Mitochondria-Targeted Vitamin E Protects Skin from UVB-Irradiation.
Won Serk KIM ; Ikyon KIM ; Wang Kyun KIM ; Ju Yeon CHOI ; Doo Yeong KIM ; Sung Guk MOON ; Hyung Keun MIN ; Min Kyu SONG ; Jong Hyuk SUNG
Biomolecules & Therapeutics 2016;24(3):305-311
Mitochondria-targeted vitamin E (MVE) is designed to accumulate within mitochondria and is applied to decrease mitochondrial oxidative damage. However, the protective effects of MVE in skin cells have not been identified. We investigated the protective effect of MVE against UVB in dermal fibroblasts and immortalized human keratinocyte cell line (HaCaT). In addition, we studied the wound-healing effect of MVE in animal models. We found that MVE increased the proliferation and survival of fibroblasts at low concentration (i.e., nM ranges). In addition, MVE increased collagen production and downregulated matrix metalloproteinase1. MVE also increased the proliferation and survival of HaCaT cells. UVB increased reactive oxygen species (ROS) production in fibroblasts and HaCaT cells, while MVE decreased ROS production at low concentration. In an animal experiment, MVE accelerated wound healing from laser-induced skin damage. These results collectively suggest that low dose MVE protects skin from UVB irradiation. Therefore, MVE can be developed as a cosmetic raw material.
Animal Experimentation
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Cell Line
;
Collagen
;
Fibroblasts
;
Humans
;
Keratinocytes
;
Mitochondria
;
Models, Animal
;
Reactive Oxygen Species
;
Skin*
;
Vitamin E*
;
Vitamins*
;
Wound Healing
5.The EC50 of remifentanil to minimize the cardiovascular changes during head holder pinning in neurosurgery.
Wang Seok DO ; Tae Kyun KIM ; Hae Kyu KIM ; Cheul Hong KIM
Korean Journal of Anesthesiology 2012;63(4):327-333
BACKGROUND: During neuroanesthesia, head holder pinning commonly results in sympathetic stimulation manifested by hemodynamic changes, such as increased heart rate and arterial blood pressure. Remifentanil has been used successfully to control acute autonomic responses during neurosurgical procedures. The objective of this study was to determine effect-site concentration of remifentanil for suppressing the hemodynamic response to head holder pinning with the probability of 50% (EC50). METHODS: Forty-one ASA physical status I or II patients, between the ages of 20-70, who were scheduled for neurosurgery were recruited into this study. After arrival in the operating room, standard monitoring was applied throughout the study, which included a bispectral index monitor. Both propofol and remifentanil were administered by Target-control infusion device. The Dixon "up-and-down" sequential allocation method was used to determine the EC50 of remifentanil. RESULTS: The EC50 of remifentanil was 2.19 +/- 0.76 ng/ml by the turning point estimate (TPE). In probit analysis, EC50 was 2.42 ng/ml (95% CI : -0.62-4.66) and EC95 was 5.70 ng/ml (95% CI : 4.02-67.53). The EC50 estimator comes from isotonic regression is 2.90 ng/ml (95% CI : 1.78-3.65). The EC95 estimator comes from isotonic regression is 4.28 ng/ml (95% CI : 3.85-4.41). CONCLUSIONS: This study showed that EC50 of remifentanil was 2.19 +/- 0.76 ng/ml by TPE. EC50 was 2.42 ng/ml (95% CI -0.62-4.66) in probit analysis, as back up analysis. The EC50 estimator comes from isotonic regression is 2.90 ng/ml (95% CI : 1.78-3.65).
Arterial Pressure
;
Consciousness Monitors
;
Head
;
Heart Rate
;
Hemodynamics
;
Humans
;
Neurosurgery
;
Neurosurgical Procedures
;
Operating Rooms
;
Organothiophosphorus Compounds
;
Piperidines
;
Propofol
6.The Anti-tumor Activity of Vitamin C via the Increase of Fas (CD95) and MHC I Expression on Human Stomach Cancer Cell Line, SNU1.
Yeonsil YU ; Seyeon BAE ; Hyemin KIM ; Yejin KIM ; Nag Bum CHU ; Nag Kyun CHU ; Jae Seung KANG ; Wang Jae LEE
Immune Network 2011;11(4):210-215
BACKGROUND: It is already known that high concentration of vitamin C induces apoptosis on tumor cells. However, there is no report regarding the function of vitamin C on the modulation of immune susceptibility of cancer. Therefore, we investigated whether vitamin C can modulate immune susceptibility of tumor cells, especially on the induction of Fas-mediated apoptosis. METHODS: First, the optimal concentration of vitamin C, which cannot induce damages on tumor cells for 36 hrs. We found that 2 mM of vitamin C did not show harmful effect. In addition, the optimal concentration of agonistic anti-Fas Abs for 18 hrs was examined. RESULTS: As a result, 400 ng/ml of agonistic anti-Fas Abs did not induce apoptosis on tumor cells. Next, we tried to find the effect of 2 mM of vitamin C on the modulation of the susceptibility to agonistic anti-Fas Abs. When tumor cells were cultured with 400 ng/ml of agonistic anti-Fas Abs for 18 hrs, after pre-treatment with 2 mM of vitamin C for 24 hrs, viability of cells was decreased. Interestingly, we found that the expression of Fas (CD95) and MHC class I was increased by the treatment of vitamin C. CONCLUSION: Taken together, vitamin C increases the susceptibility of tumor cells to anti-Fas Abs and the expression of Fas (CD95) and MHC class I on tumor cells.
Apoptosis
;
Ascorbic Acid
;
Cell Line
;
Humans
;
Stomach
;
Stomach Neoplasms
;
Vitamins
7.The Effect of Chlamydia pneumoniae on the Expression of Peroxisome Proliferator-Activated Receptor-gamma in Vascular Smooth Muscle Cells.
Yong Hwan KIM ; Si Young CHOI ; Jong Hui SUH ; Tae Kyun KIM ; Ki Bae SEUNG ; Young Pil WANG ; Kiyuk CHANG
Yonsei Medical Journal 2008;49(2):230-236
PURPOSE: This study was designed to investigate the change of peroxisome proliferator-activated receptor gamma (PPARgamma) after the infection of the human coronary artery smooth muscle cells (HCSMCs) with Chlamydia pneumoniae (C. pneumoniae) and the effect of PPARgamma agonist on the expression of PPARgamma of C. pneumoniae-infected HCSMCs. MATERIALS AND METHODS: To determine the effect of PPARgamma agonist on the proliferation of C. pneumoniae-infected HCSMCs, rosiglitazone at various concentrations was applied 1 hour before inoculation of HCSMCs. RESULTS: The expression of PPARgamma mRNA in HCSMCs increased from 3 hours after C. pneumoniae infection and reached that of noninfected HCSMCs at 24 hours (p < 0.05). The expression of PPARgamma protein in HCSMCs also increased from 3 hours after C. pneumoniae and persisted until 24 hours as compared with that of noninfected HCSMCs (p < 0.05). The pretreatment of HCSMCs with rosiglitazone followed by the infection with C. pneumoniae augmented the expression of PPARgamma mRNA and protein (p < 0.05) and decreased cell proliferation. CONCLUSION: Our results showed that the expression of PPARgamma increases in response to C. pneumoniae infection and rosiglitazone further augmented the expression of PPARgamma. It is suggested that rosiglitazone could ameliorate the chronic inflammation in the vessel wall induced by C. pneumoniae by augmenting PPARgamma expression.
Blotting, Western
;
Cell Line
;
Cell Proliferation/drug effects
;
Chlamydophila pneumoniae/growth & development/*physiology
;
Gene Expression Regulation/drug effects
;
Humans
;
Muscle, Smooth, Vascular/cytology/drug effects/metabolism
;
Myocytes, Smooth Muscle/drug effects/*metabolism/microbiology
;
PPAR gamma/genetics/*metabolism
;
RNA, Messenger/genetics/metabolism
;
Reverse Transcriptase Polymerase Chain Reaction
;
Thiazolidinediones/pharmacology
8.New Paradigm for Patients with Pulmonary Nodule Expecting Thoracoscopic Resection.
Min Sub JO ; Seok Whan MOON ; Sung Bo SIM ; Young Pil WANG ; Keon Hyeon JO ; Jong Hui SUH ; Moon Sub KWACK ; Sun Hee LEE ; Hak Hee KIM ; Young Kyun KIM
The Korean Journal of Thoracic and Cardiovascular Surgery 2003;36(10):748-753
BACKGROUND: The pulmonary nodules (PN), when indicated, need thoracoscopic resection, especially in cases of non-diagnostic or technically infeasible PCNA (percutaneous needle aspiration). In the difficult situations of small or deeply seated PN, several techniques facilitating thoracoscopy have been used for detecting them. Our new protocol for managing PN was developed and prospectively reviewed. MATERIAL AND METHOD: In the procedure of PCNA, we firstly placed the tip of the needle in the center of, or just in contact with PN under CT guidance, and loaded one or two segments of platinum radiomarker inside the needle after removing the stylet. Then, we forced the radiomarker to move to the tip of the needle by pushing the stylet. Finally, if the tip of the needle was not within PN, it was reoriented to the their center to obtain the sample for PCNA. RESULT: Between May 1999 and May 2000, radiomarkers were successfully placed in 28 PN of 26 patients, with the exception of one. In 18 (85%) of 21 nodules needing throacoscopy, intraoperative fluoroscopy was used to detect them or guide stapling resection during thoracoscopy. CONCLUSION: The advantages of this technique are that there is that there is no need for further localization for thoracoscopy even in cases of unsuccessful PCNA, and it was more effective in respect to both cost and time. Therefore, this strategy for PN expecting thoracoscopy will be helpful to patients and medical staff alike.
Fluoroscopy
;
Humans
;
Medical Staff
;
Needles
;
Platinum
;
Proliferating Cell Nuclear Antigen
;
Prospective Studies
;
Thoracoscopy
9.High levels of soluble herpes virus entry mediator in sera of patients with allergic and autoimmune diseases.
Hyo Won JUNG ; Su Jin LA ; Ji Young KIM ; Suk Kyeung HEO ; Ju Yang KIM ; Sa WANG ; Kack Kyun KIM ; Ki Man LEE ; Hong Rae CHO ; Hyeon Woo LEE ; Byungsuk KWON ; Byung Sam KIM ; Byoung Se KWON
Experimental & Molecular Medicine 2003;35(6):501-508
Herpes virus entry mediator (HVEM) is a newly discovered member of the tumor necrosis factor receptor (TNFR) superfamily that has a role in herpes simplex virus entry, in T cell activation and in tumor immunity. We generated mAb against HVEM and detected soluble HVEM (SHVEM) in the sera of patients with various autoimmune diseases. HVEM was constitutively expressed on CD4(+)and CD8(+)T cells, CD19(+)B cells, CD14(+)monocytes, neutrophils and dendritic cells. In three-way MLR, mAb 122 and 139 were agonists and mAb 108 had blocking activity. An ELISA was developed to detect sHVEM in patient sera. sHVEM levels were elevated in sera of patients with allergic asthma, atopic dermatitis and rheumatoid arthritis. The mAbs discussed here may be useful for studies of the role of HVEM in immune responses. Detection of soluble HVEM might have diagnostic and prognostic value in certain immunological disorders.
Animals
;
Antibodies, Monoclonal/immunology
;
Antibody Specificity
;
Arthritis, Rheumatoid/blood/immunology
;
Asthma/blood/immunology
;
Autoimmune Diseases/*blood/immunology
;
Cell Division
;
Cell Line
;
Dermatitis, Atopic/blood/immunology
;
Female
;
Flow Cytometry
;
Humans
;
Hypersensitivity/*blood/immunology
;
Lymphocyte Culture Test, Mixed
;
Mice
;
Mice, Inbred BALB C
;
Receptors, Tumor Necrosis Factor/*blood/immunology
;
Receptors, Tumor Necrosis Factor, Member 14
;
Receptors, Virus/*blood/immunology
;
Solubility
10.A Case of Fibrolipoma.
Young Tae KIM ; Wan Soo KIM ; Young Lip PARK ; Mun Kyun CHO ; Kyu Wang HWANG
Korean Journal of Dermatology 2003;41(7):939-941
Fibrolipoma is a rare variant of lipomas which shows distinct pathologic findings with both component of mature adipose cells and broad bands of dense fibrous connective tissue. A 52-year-old woman presented with 2X2cm sized, indurated, slightly elevated and slightly tender subcutaneous mass which slowly enlarged during the last four to five years accompanied by slight tenderness on the right upper back. The laboratory examination showed non-specific findings. Histopathologic findings revealed a well-defined mass composed of eosinophilic dense connective tissue bands with mature adipose cells scattered throughout the mass. The lesion was totally excised and she showed no evidence of recurrence after 6 months of follow-up.
Connective Tissue
;
Eosinophils
;
Female
;
Follow-Up Studies
;
Humans
;
Lipoma
;
Middle Aged
;
Recurrence

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