Green Coffea arabica Extract Ameliorates Testicular Injury in High-Fat Diet/Streptozotocin-Induced Diabetes in Rats

J Diabetes Res. 2020 Jun 12:2020:6762709. doi: 10.1155/2020/6762709. eCollection 2020.

Abstract

Diabetes mellitus (DM) is a chronic endocrine disease characterized by persistent hyperglycemia. Oxidative damage, inflammatory cytokines, and apoptotic cell death play a major role in the induction and progression of male testicular damage. Plant-derived phytochemicals such as green coffee (Coffea arabica) can possess antidiabetic effects with little toxicity. The current study is aimed at investigating the therapeutic roles of green coffee in diabetic testicular injury stimulated by high-fat diet/streptozotocin administration. Diabetes mellitus was induced by a high-fat diet and a single dose of streptozotocin (STZ) (35 mg kg-1) in male albino rats. Diabetic animals were orally given two different concentrations of green coffee (50 mg kg-1 and 100 mg kg-1) for 28 days. The levels of testosterone, luteinizing hormone, and follicle-stimulating hormone and parameters of oxidative stress, inflammation, and apoptosis were measured. mRNAs and protein levels were detected quantitatively by real-time PCR and ELISA, respectively. In the diabetic group, the levels of testosterone, luteinizing hormone, and follicle-stimulating hormone showed a significant reduction while they increased significantly after green coffee treatment. A significant increase of antioxidant markers glutathione, superoxide dismutase, catalase, glutathione peroxidase, and glutathione reductase along with decreased levels of lipid peroxides and nitric oxide was observed after green coffee treatment in the diabetic group. Finally, the levels of IL-1β, TNF-α, Bax, and caspase-3 were also decreased in both treated groups (metformin and green coffee) when compared to the diabetic group. We conclude that testicular oxidative impairment induced by a high-fat diet (HFD) and STZ can be reversed by green coffee. Administration of green coffee could represent a promising therapeutic agent which can help the treatment of type 2 DM-induced testicular dysfunction.

MeSH terms

  • Animals
  • Apoptosis / drug effects*
  • Caspase 3 / drug effects
  • Caspase 3 / metabolism
  • Catalase / drug effects
  • Catalase / metabolism
  • Coffea*
  • Diabetes Complications / metabolism*
  • Diabetes Mellitus, Experimental / metabolism*
  • Diet, High-Fat
  • Enzyme-Linked Immunosorbent Assay
  • Follicle Stimulating Hormone / metabolism
  • Glutathione / drug effects
  • Glutathione / metabolism
  • Glutathione Peroxidase / drug effects
  • Glutathione Peroxidase / metabolism
  • Glutathione Reductase / drug effects
  • Glutathione Reductase / metabolism
  • Hypoglycemic Agents / pharmacology
  • Inflammation / metabolism
  • Interleukin-1beta / drug effects
  • Interleukin-1beta / metabolism
  • Lipid Peroxidation / drug effects
  • Luteinizing Hormone / drug effects
  • Luteinizing Hormone / metabolism
  • Male
  • Metformin / pharmacology
  • Nitric Oxide / metabolism
  • Oxidative Stress / drug effects*
  • Plant Extracts / pharmacology*
  • RNA, Messenger
  • Rats
  • Real-Time Polymerase Chain Reaction
  • Streptozocin / toxicity
  • Superoxide Dismutase / drug effects
  • Superoxide Dismutase / metabolism
  • Testicular Diseases / metabolism*
  • Testis / drug effects*
  • Testis / metabolism
  • Testosterone / metabolism
  • Tumor Necrosis Factor-alpha / drug effects
  • Tumor Necrosis Factor-alpha / metabolism
  • bcl-2-Associated X Protein / drug effects
  • bcl-2-Associated X Protein / metabolism

Substances

  • Bax protein, rat
  • Hypoglycemic Agents
  • IL1B protein, rat
  • Interleukin-1beta
  • Plant Extracts
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha
  • bcl-2-Associated X Protein
  • Nitric Oxide
  • Testosterone
  • Streptozocin
  • Luteinizing Hormone
  • Follicle Stimulating Hormone
  • Metformin
  • Catalase
  • Glutathione Peroxidase
  • Superoxide Dismutase
  • Glutathione Reductase
  • Casp3 protein, rat
  • Caspase 3
  • Glutathione