Gosha-Jinki-Gan Improved Erectile Dysfunction Caused by Anti-Cancer Agent Oxaliplatin by Decreasing Transcriptional Expression of Phosphodiesterase-5 in Rats

Abstract

Background: A platinum-containing anti-cancer agent, oxaliplatin (L-OHP), is known to induce peripheral neuropathy, including erectile dysfunction (ED) as a side effect, while Gosha-jinki-gan (GJG) is a traditional Japanese herbal medicine mainly used for peripheral neuropathy. Aim: To investigate the effect of GJG on L-OHP-induced ED in rats. Methods: Twelve-week-old male Wister/ST rats were categorized into the following groups: Sham, Sham+GJG, L-OHP, and L-OHP+GJG (each n = 10). The L-OHP and L-OHP+GJG groups were injected intravenously with L-OHP (4 mg/ kg) for 2 consecutive days in the first week. Statistical significance was determined using Bonferroni's multiple comparison test. Outcomes: At the end of the study period, erectile function was evaluated by measuring intracavernosal pressure (ICP) and mean arterial pressure (MAP) after cavernous nerve stimulation. Western blot analysis was used to assess the neuronal nitric oxide synthase (nNOS) and endothelial nitric oxide synthase (eNOS) levels, and quantitative polymerase chain reaction was used to assess the expression of phosphodiesterase-5 (PDE-5) and nicotinamide adenine dinucleotide phosphate (NADPH) oxidase-1. Results: The ICP/MAP ratio of L-OHP rats (0.34 § 0.06) was significantly lower than that of Sham rats (0.67 § 0.03, P < .01), however, the ICP/MAP ratio of L-OHP+GJG rats (0.55 § 0.01) was significantly higher than that of L-OHP rats (P < .01). There were no significant differences in the nNOS and eNOS protein expression between both groups (P > .05). GJG administration significantly decreased PDE-5 and NADPH oxidase-1 messenger RNA expressions in the L-OHP+GJG group. Clinical Translation: This animal model study suggests that GJG might be effective for erectile function in cancer survivors.Strengths & limitations: Our study identified that GJG had no notable side effects in the treated group. Further investigation of the cavernous nerve would also help elucidate the mechanism of GJG effect, which is a limitation of this study. Conclusion: We found that GJG administration improved L-OHP-induced ED by improving transcriptional

Exploring the application of sildenafil for high-fat diet-induced erectile dysfunction based on interleukin-18-mediated NLRP3/Caspase-1 signaling pathway

“…The measurement of mean artery pressure (MAP) and intracavernous pressure (ICP) was used to evaluate erectile function. 21 , 22 Rats’ exposed left carotid arteries were cannulated with a PE-50 tube filled with 250 IU/mL heparinized saline and connected to a pressure channel to continuously measure MAP. A lower midline abdominal incision in rats exposed both the penile crus and cavernous nerve.…”

Establishment of mouse line showing inducible priapism‐like phenotypes

“…Intracavernous pressure (ICP) elicited by electrical stimulation was previously described. 34 In brief, mice are anesthetizedby 4% isoflurane for induction, and 1.5–2.0% isoflurane for maintenance using an inhalationanesthesia apparatus (Nakazawa Seisaku‐sho, Funabashi, Japan). The left crus of the corpuscavernosum (CC) was cannulated using a 23‐G needle for continuous ICP monitoring.…”