Nanoparticles of Antroquinonol-Rich Extract from Solid-State-Cultured Antrodia cinnamomea Improve Reproductive Function in Diabetic Male Rats

Int J Nanomedicine. 2020 Jun 15:15:4191-4203. doi: 10.2147/IJN.S252885. eCollection 2020.

Abstract

Purpose: To characterize the nanoparticle of antroquinonol from A. cinnamomea and its ameliorative effects on the reproductive dysfunction in the diabetic male rat.

Material and methods: The chitosan-silicate nanoparticle was used as the carrier for the delivery of antroquinonol from solid-state-cultured A. cinnamomea extract (AC). The rats were fed with a high-fat diet and intraperitoneally injected with streptozotocin to induce diabetes. The rats were daily oral gavage by water [Diabetes (DM) and Control groups], three different doses of chitosan-silicate nanoparticle of antroquinonol from solid-state-cultured A. cinnamomea (nano-SAC, NAC): (DM+NAC1x, 4 mg/kg of body weight; DM+NAC2x, 8 mg/kg; and DM+NAC5x, 20 mg/kg), solid-state-cultured AC (DM+AC5x, 20 mg/kg), or metformin (DM+Met, 200 mg/kg) for 7 weeks.

Results: The nano-SAC size was 37.68±5.91 nm, the zeta potential was 4.13±0.49 mV, encapsulation efficiency was 79.29±0.77%, and loading capacity was 32.45±0.02%. The nano-SAC can improve diabetes-induced reproductive dysfunction by regulating glucose, insulin, and oxidative enzyme and by increasing the level of testosterone, follicle-stimulating hormone, luteinizing hormone, and sperm count as well as sperm mobility. In testicular histopathology, the seminiferous tubules of A. cinnamomea-supplemented diabetic rats showed similar morphology with the control group.

Conclusion: The nanoparticle of antroquinonol from Antrodia cinnamomea can be used as an effective strategy to improve diabetes-induced testicular dysfunction.

Keywords: Antrodia cinnamomea; antroquinonol; diabetes; male reproduction; nanoparticles.

MeSH terms

  • Animals
  • Antrodia / chemistry*
  • Blood Glucose / metabolism
  • Diabetes Mellitus, Experimental / blood
  • Diabetes Mellitus, Experimental / drug therapy*
  • Diabetes Mellitus, Experimental / pathology
  • Disease Models, Animal
  • Fasting / blood
  • Glutathione Peroxidase / metabolism
  • Humans
  • Insulin / adverse effects
  • Insulin / blood
  • Kidney / drug effects
  • Kidney / physiopathology
  • Liver / drug effects
  • Liver / physiopathology
  • Male
  • Malondialdehyde / metabolism
  • Nanoparticles / chemistry*
  • Oxidative Stress / drug effects
  • Rats, Sprague-Dawley
  • Reproduction*
  • Sperm Count
  • Sperm Motility / drug effects
  • Streptozocin
  • Superoxide Dismutase / metabolism
  • Testis / drug effects
  • Testis / pathology
  • Ubiquinone / analogs & derivatives*
  • Ubiquinone / pharmacology
  • Ubiquinone / therapeutic use

Substances

  • Blood Glucose
  • Insulin
  • Ubiquinone
  • Malondialdehyde
  • Streptozocin
  • antroquinonol
  • Glutathione Peroxidase
  • Superoxide Dismutase