Min Jung Park

Dr. Min Jung Park


Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

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

Representative Publications

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22 April 2021 in Reproductive Biology and Endocrinology
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Journal Article
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HLHyun Joo Lee
Hyun Joo Lee
MPMin Jung Park
Min Jung Park
Bo Sun JooBo Sun Joo
Bo Sun Joo
JJJongkil Joo
Jongkil Joo
YKYeon Hee Kim
Yeon Hee Kim
KKKi Hyung Kim
Ki Hyung Kim
Background: Several studies have shown that coenzyme Q10 (CoQ10) can rescue ovarian aging and that ovarian surface epithelium (OSE)-derived ovarian stem cells (OSCs) are useful for treating infertility due to ovarian aging. However, few studies have examined the effect of CoQ10 on OSCs. This study was aimed to investigate whether CoQ10 activates OSCs and recovers ovarian function in a 4-vinylcyclohexene diepoxide (VCD)-induced mouse model of ovarian failure.Methods: Forty female C57BL/6 mice aged 6 weeks were randomly divided into four groups (n = 10/group): a control group administered saline orally, a CoQ10 group administered 150 mg/kg/day of CoQ10 orally in 1 mL of saline daily for 14 days, a VCD group administered 160 mg/kg/day of VCD i.p. in 2.5 mL of saline/kg for 5 days, and a VCD + CoQ10 group administered VCD i.p. for 5 days injection and CoQ10 (150 mg/kg/day) orally for 14 days. After treatment, follicle counts were evaluated by hematoxylin and eosin (H&E) staining, and ovarian mRNA expressions of Bmp-15, Gdf-9, and c-Kit were examined by quantitative real-time PCR. Serum FSH, AMH, and ROS levels were also measured. Oocyte-like structure counts and the expressions of Oct-4 and MVH were also evaluated after culturing OSE for 3 weeks. In a second experiment, 32 female mice were administered CoQ10 as described above, induced to superovulate using PMSG and hCG, and mated. Numbers of zygotes and embryo development rate were examined.Results: Postcultured OSE showed significant increases in the numbers of oocyte-like structure and that the expression of Oct-4 and MVH were higher in the VCD + CoQ10 group than in the VCD group (p < 0.05). Numbers of surviving follicles from primordial to antral follicles, numbers of zygotes retrieved and embryo development rate to blastocyst were significantly greater in the VCD + CoQ10 group than in the VCD group (p < 0.01). Serum AMH level and ovarian expressions of Bmp-15, Gdf-9 and c-Kit were also significantly greater in the VCD + CoQ10 group than in the VCD group (p < 0.05). In contrast, serum ROS level was significantly lower in the VCD + CoQ10 group than in the VCD group (p < 0.05).Conclusion: This study shows that CoQ10 stimulates the differentiation of OSE-derived OSCs and confirms that CoQ10 can reduce ROS levels and improve ovarian function and oocyte quality in mice with VCD-induced ovarian failure.

1 January 2023 in The World Journal of Men's Health
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Journal Article
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KKKyung Hwan Kim
Kyung Hwan Kim
MPMin Jung Park
Min Jung Park
NPNam Cheol Park
Nam Cheol Park
HPHyun Jun Park
Hyun Jun Park
Kim KH, et al. World J Mens Health. 2023 Jan;41:e1. https://doi.org/10.5534/wjmh.220100

1 January 2017 in The World Journal of Men's Health
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HPHyun Jun Park
Hyun Jun Park
SKSUKJIN KIM
SUKJIN KIM
MPMin Jung Park
Min Jung Park
YHYoon Kyung Hwang
Yoon Kyung Hwang
SHSung Yeoun Hwang
Sung Yeoun Hwang
NPNam Cheol Park
Nam Cheol Park
Park HJ, et al. World J Mens Health. 2017 Sep;35:e12. https://doi.org/10.5534/wjmh.17031

1 January 2020 in Animal Reproduction
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Journal Article
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MPMin Jung Park
Min Jung Park
SHSi-Eun Han
Si-Eun Han
HKHyeon Jeong Kim
Hyeon Jeong Kim
JHJeong Doo Heo
Jeong Doo Heo
HCHee-Jung Choi
Hee-Jung Choi
Bo Sun JooBo Sun Joo
Bo Sun Joo
Although ovarian aging is a key cause of decreased ovarian function and oocyte quality, it remains a problem in infertility treatment. Therefore, this study is aimed to investigate whether Paeonia lactiflora (PL), a herb improves ovarian function and oocyte quality using aged female mice. C57BL/6 female mice aged 8 months were treated orally every day with PL of 26.5 mg/kg (n=7) and 53 mg/kg (n=7) of body weight for 4 weeks using an oral zoned needle. The control group (n=7) was treated with normal saline. Ovaries and serum were collected for the H&E stain and the evaluation of reactive oxygen species (ROS) levels, respectively. In the second experiment, female mice were orally administered with PL (26.5 mg/kg: n=12, 53 mg/kg: n=12, control: n=12) and then superovulated with PMSG and hCG, and mated with male mice. Zygotes were retrieved and cultured for 4 days. Ovaries were provided for examination of expressions of genes associated with angiogenesis (VEGF and visfatin), anti-aging (Sirt1 and Sirt2), and follicular development (c-Kit, BMP-15, and GDF-9). PL significantly increased numbers of surviving follicles (primordial, primary, secondary, and antral), numbers of zygotes retrieved, embryo development rate, and ovarian expression of VEGF, visfatin, c-Kit, BMP-15, and GDF-9 at both doses. However, ovarian expression of Sirt1 and Sirt2 was increased at 53.0 mg/kg of PL. ROS levels were not affected by PL. These results suggest that PL may possess beneficial effects regarding ovarian function and oocyte quality, possibly by activation of ovarian angiogenesis and follicular development.

29 December 2012 in Reproductive Biology and Endocrinology
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Journal Article
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SPSeung S Park
Seung S Park
MPMin Jung Park
Min Jung Park
BJBo S Joo
Bo S Joo
JJJongkil Joo
Jongkil Joo
JSJung B Son
Jung B Son
SYSooseong You
Sooseong You
Background: Advancing female age remains a difficult problem in infertility treatment. Ovarian angiogenesis plays an important role in follicular development and the activation of ovarian angiogenesis has been emerged as a new strategy for the improvement of age-related decline of oocyte quality. BMP-6 affect gonadotropin signals in granulosa cells and it promotes normal fertility by enabling appropriate response to LH and normal oocyte quality. BMP-6 has a potential role in regulation of angiogenesis and regulates the expression of inhibitor of DNA-binding proteins (Ids). Ids involved in the control and timing of follicle selection and granulosa cells differentiation. Especially, Id-1 is well-characterized target of BMP-6 signaling. Therefore, this study investigated whether co-administration of BMP-6 during superovulation process improves ovarian response, oocyte quality and expression of Id-1 and vascular endothelial growth factor (VEGF) in the ovary of aged female using a mouse model. Methods: Aged C57BL/6 female mice (26–31 weeks old) were superovulated by injection with 0.1 mL of 5 IU equine chorionic gonadotropin (eCG) containing recombinant mouse BMP-6 at various doses (0, 0.01, 0.1, 1, and 10 ng), followed by injection with 5 IU human chorionic gonadotropin (hCG) 48 h later. Then, the mice were immediately paired with an individual male. The aged control group was superovulated without BMP-6. Young mice of 6–9 weeks old were superovulated without BMP-6 as a positive control for superovulation and in vitro culture of embryos. Eighteen hours after hCG injection, zygotes were retrieved and cultured for 4 days. Both ovaries of each mouse were provided in the examination of ovarian expression of Id-1 and VEGF by reverse transcriptase-polymerase chain reaction, western blot, and immunohistochemistry. Results: Administration of 0.1 ng BMP-6 significantly increased the number and blastocyst formation rate of oocytes ovulated and ovarian expression of Id-1 and VEGF compared to aged control mice. These increased levels were comparable to those of young control mice. Conclusions: This result suggests that BMP-6 during ovulation induction plays an important role in improvement of oocyte quality and ovarian response of aged female, possibly by regulating of ovarian Id-1 and VEGF expression.

1 January 2019 in The World Journal of Men's Health
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Journal Article
Open access
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MPMin Jung Park
Min Jung Park
HPHyun Jun Park
Hyun Jun Park
WCWon Hee Cheon
Won Hee Cheon
JPJih Hoon Park
Jih Hoon Park
BSByung-Cheul Shin
Byung-Cheul Shin
NPNam Cheol Park
Nam Cheol Park
Park MJ, et al. World J Mens Health. 2019 Jan;37:e53. https://doi.org/10.5534/wjmh.190091