Effects of Ganoderma Lucidum shell-broken spore on oxidative stress of the rabbit urinary bladder using an in vivo

Robert M Levin1,2, Li Xia3, Wu Wei3

  • 1Stratton VA Medical Center, Albany, NY, 12208, USA. Robert.levin2@va.gov.

Insights

Ganoderma Lucidum (GL) effectively protected rabbit bladder function against oxidative stress from ischemia/reperfusion (I/R) injury. This study provides evidence for GL

Area of Science:

  • Pharmacology
  • Oxidative Stress Research
  • Urology

Background:

  • Oxidative stress is implicated in aging and disease pathophysiology.
  • Herbal remedies have historically been used for health, but lack modern scientific validation.
  • Benign prostatic hyperplasia (BPH) causes urinary bladder dysfunction in aging men, linked to oxidative stress.

Purpose of the Study:

  • To evaluate the protective effects of Ganoderma Lucidum (GL) against in vivo ischemia/reperfusion (I/R) induced oxidative stress.
  • To investigate GL's ability to preserve bladder function under I/R conditions.
  • To provide scientific evidence for the antioxidant and protective properties of GL.

Main Methods:

  • Utilized an established rabbit model of ischemia/reperfusion (I/R) injury.
  • Administered Ganoderma Lucidum (GL) as a pretreatment to rabbits.
  • Assessed bladder compliance and contractile responses following I/R insult.

Main Results:

  • Ischemia/reperfusion (I/R) significantly reduced bladder compliance and contractile function.
  • Pretreatment with Ganoderma Lucidum (GL) completely prevented the detrimental effects of I/R on bladder function.
  • GL demonstrated significant protection against oxidative stress-induced damage.

Conclusions:

  • Ganoderma Lucidum (GL) offers substantial protection to bladder function against ischemia/reperfusion (I/R) mediated oxidative stress.
  • GL's antioxidant properties are effective in mitigating I/R-induced damage in a relevant animal model.
  • These findings support the use of Ganoderma Lucidum for preventing oxidative stress-related bladder dysfunction.

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