Jin-Ok Ahn

Dr. Jin-Ok Ahn

orcid

Research Focus & Metrics

Academic Career Length

7Years (2020-Present)

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

Representative Publications

View All Publications
1 January 2021 in Journal of Veterinary Science
Verified
Journal Article
Open access
PDF file
SPSeol-Gi Park
Seol-Gi Park
JAJu-Hyun An
Ju-Hyun An
QLQIANG LI
QIANG LI
HCHyung-Kyu Chae
Hyung-Kyu Chae
SPSu-Min Park
Su-Min Park
HYHwa-Young Youn
Hwa-Young Youn
Park SG, et al. J Vet Sci. 2021 Feb;22(2):e16. https://doi.org/10.4142/jvs.2021.22.e16

Verified
Journal Article
Open access
PDF file
SLSeokwoo Lee
Seokwoo Lee
NLNa Yeon Lim
Na Yeon Lim
MKMin Soo Kang
Min Soo Kang
YJYunho Jeong
Yunho Jeong
JAJin-Ok Ahn
Jin-Ok Ahn
JCJin-Young Chung
Jin-Young Chung
Atopic dermatitis (AD) is a common chronic inflammatory skin disease. Interleukin 31 (IL-31), a novel cytokine in AD, causes pruritus, typically characteristic of AD patients. The transient receptor potential vanilloid type 1 (TRPV1) is a cation channel activated by diverse noxious stimuli that has been studied in a variety of pruritic skin diseases. In this study, the AD animal model was generated by administering the hapten, trinitrochlorobenzene (TNCB), to Nc/Nga mice, and the degree of expression of the IL-31 receptor alpha (IL-31RA) and TRPV1 in the skin of these atopic models was evaluated. The Nc/Nga mice were divided into 3 groups: control, TNCB 2-weeks treated, and TNCB 8-weeks treated. After inducing AD, the skin lesions in each group were scored and compared, and the histology of the skin lesions and the IL-31RA and TRPV1 expression for each group were evaluated by analyzing immunohistochemistry. The results show a significant difference in the skin lesion scores between the groups. The immunohistochemistry evaluation highlighted the remarkable expression of IL-31RA and TRPV1 in the nerve fibers of the TNCB 8-weeks-treated group. We thus confirmed that the long-term application of TNCB induced chronic atopic-like dermatitis and that IL-31RA and TRPV1 were overexpressed in the peripheral nerve fibers in this AD model.

26 March 2021 in Nutrients
Verified
Journal Article
Open access
PDF file
YKYoonhwan Kim
Yoonhwan Kim
MKMin Soo Kang
Min Soo Kang
TKTae Hyeong Kim
Tae Hyeong Kim
YJYunho Jeong
Yunho Jeong
JAJin-Ok Ahn
Jin-Ok Ahn
JCJin-Young Chung
Jin-Young Chung
Many trials have been conducted to treat atopic dermatitis (AD), but these therapies are generally unsuccessful because of their insufficiency or side effects. This study examined the efficacy of β-glucan derived from oats with fermented probiotics (called Synbio-glucan) on an AD-induced mouse model. For the experiment, Nc/Nga mice were exposed to a house dust mite extract (HDM) to induce AD. The mice were placed in one of four groups: positive control group, Synbio-glucan topical treatment group, Synbio-glucan dietary treatment group, and Synbio-glucan topical + dietary treatment group. The experiment revealed no significant difference in the serum IgE concentration among the groups. Serum cytokine antibody arrays showed that genes related to the immune response were enriched. A significant difference in the skin lesion scores was observed between the groups. Compared to the control group tissue, skin lesions were alleviated in the Synbio-glucan topical treatment group and Synbio-glucan dietary treatment group. Interestingly, almost normal structures were observed within the skin lesions in the Synbio-glucan topical + dietary treatment group. Overall, the β-glucan extracted from oats and fermented probiotic mixture is effective in treating atopic dermatitis.

1 January 2020 in Journal of Veterinary Science
Verified
Journal Article
Open access
YKYoonhwan Kim
Yoonhwan Kim
TKTae Hyeong Kim
Tae Hyeong Kim
MKMin Soo Kang
Min Soo Kang
JAJin-Ok Ahn
Jin-Ok Ahn
JCJung Hoon Choi
Jung Hoon Choi
JCJin-Young Chung
Jin-Young Chung
Kim YH, et al. J Vet Sci. 2019 Oct;21:e59. https://doi.org/10.4142/jvs.2020.21.e59

18 March 2021 in Veterinary Sciences
Verified
Journal Article
Open access
PDF file
SCSoon-Won Choi
Soon-Won Choi
YKYoonhwan Kim
Yoonhwan Kim
MKMin Soo Kang
Min Soo Kang
YJYunho Jeong
Yunho Jeong
JAJin-Ok Ahn
Jin-Ok Ahn
JCJin-Young Chung
Jin-Young Chung
Acute pancreatitis is an acute inflammatory process in the pancreas that is common in dogs. This study was designed to compare cytokines between healthy dogs and dogs with suspected acute pancreatitis. For the canine cytokine antibody array, three healthy dogs and three dogs with suspected acute pancreatitis were included. Interleukin (IL)-2, IL-6, IL-10, GM-CSF, and TNF-α were not detected in either group based on the results. Conversely, IL-8 (p = 0.035), Monocyte Chemoattractant Protein-1 (MCP)-1 (p = 0.0138), Receptor for Advanced Glycation Endproducts (RAGE) (p = 0.0079), and stem cell factor (SCF) (p = 0.034) were significantly increased in dogs with suspected acute pancreatitis. However, vascular endothelial growth factor (VEGF) (p = 0.6971) did not differ significantly between groups. For the canine serum Enzyme-Linked Immunosorbent Assay (ELISA), eight healthy dogs and eight dogs with suspected acute pancreatitis were included. ELISA revealed that IL-8 (p < 0.0001), MCP-1 (p < 0.0001), RAGE (p = 0.006), and SCF (p = 0.0002) were all significantly upregulated in the experimental group. We confirmed multiple patterns of cytokines in suspected acute pancreatitis of dogs via canine cytokine antibody array using a small quantity of serum. After this procedure, we reevaluated the cytokines, which were significantly increased in dogs with suspected acute pancreatitis, by ELISA, with more samples. Through this study, we confirmed that MCP-1, RAGE, and SCF were newly suggested factors in dogs with suspected acute pancreatitis.

1 January 2024 in Journal of Veterinary Science
Verified
Journal Article
Open access
PDF file
EJEunji Jeong
Eunji Jeong
JCJin-Young Chung
Jin-Young Chung
JAJin-Ok Ahn
Jin-Ok Ahn
HCHojung Choi
Hojung Choi
YLYoungwon Lee
Youngwon Lee
SCSooyoung Choi
Sooyoung Choi
Jeong E, et al. J Vet Sci. 2024 May;25(3):e37. https://doi.org/10.4142/jvs.24038