Lycium chinense Mill improves hypogonadism via anti-oxidative stress and anti-apoptotic effect in old aged rat model

Hyun Cheol Jeong, Seung Hwan Jeon, Zhu Guan Qun, Fahad Bashraheel, Sae Woong Choi, Su Jin Kim, Woong Jin Bae, Hyuk Jin Cho, U. Syn Ha, Sung Hoo Hong, Ji Youl Lee, Seong Bin Hong, Sae Woong Kim

Research output: Contribution to journalArticlepeer-review

16 Scopus citations

Abstract

Purpose: To evaluate the pharmacological effects of goji berry (Lycium chinense P. Mill) in an animal model of late-onset hypogonadism (LOH). Materials and methods: Thirty 18-month-old male Sprague–Dawley (SD) rats were used as the LOH aged rat model. Rats were divided into five groups: a control group (n = 6), low concentration goji berry extract group (150 mg/kg/day) (n = 6), high concentration goji berry extract group (300 mg/kg/day) (n = 6), low concentration goji berry complex extract group (150 mg/kg/day) (n = 6), and high goji berry complex concentration extract group (300 mg/kg/day) (n = 6). After six weeks of treatment, sperm counts and motility, serum testosterone level, androgen receptor (AR) expression, oxidative stress marker, and apoptotic factors were examined. Results: Goji berry extracts increased testosterone level to 2.07 ± 0.06 pmol/L in the goji berry 150 mg/kg group, 2.39 ± 0.08 pmol/L in the goji berry 300 mg/kg group, 2.97 ± 0.03 pmol/L in the goji berry complex 150 mg/kg group, and 3.34 ± 0.04 pmol/L in the goji berry complex 300 mg/kg group compared to 1.86 ± 0.03 pmol/L in the control group, respectively (p <.05). AR expressions were increased in testis tissue significantly but were not significant in prostate tissue. Conclusions: Goji berry might improve LOH by reversing testicular dysfunction via an anti-oxidative stress mechanism without inducing prostate disease.

Original languageEnglish
Pages (from-to)287-296
Number of pages10
JournalAging Male
Volume23
Issue number4
DOIs
StatePublished - 2020

Bibliographical note

Funding Information:
This work was supported by the Technological Innovation R&D Program [S2198495] funded by the Small and Medium Business Administration (SMBA, Korea). This research was supported by the Bio & Medical Technology Development Program of the National Research Foundation (NRF) funded by the Ministry of Science & ICT [NRF-2018M3A9E8020861].

Publisher Copyright:
© 2018 Informa UK Limited, trading as Taylor & Francis Group.

Keywords

  • animal model
  • Antioxidant
  • goji berry
  • late-onset hypogonadism
  • testosterone

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