Erectile dysfunction (ED) as a common problem in the field of urology and andrology has huge negative effects on patients’ quality of life (1,2). Although multi-etiological factors have been found to be involved in the progression of ED (3), nerve damage and recovery have been proven to be a vital component in the development and management of ED (4). This has been proven in clinical scenarios as organic ED is found to be more frequent among the aging population, patients after pelvic surgery, patients with cardiovascular disease, and patients with diabetes, most of which involve nerve injury or degeneration. Meanwhile, ED patients with nerve damage usually respond poorly to conventional ED treatments (5,6), such as phosphodiesterase 5 inhibitors (PDE5is), the widely prescribed medications for the “symptomatic treatment” of ED (7,8). Owing to the fact that none of the current ED interventions could fully “reverse” the pathological changes, especially the nerve damage in ED (9), the pursue to find curable treatment has been carried forward enthusiastically.
A complete neural network is the initiating and maintaining factor for normal erection, but nerve regeneration after injury is known for its slow speed and high uncertainty (4,10). Meanwhile, cavernous nerve regeneration has its unique characteristics. After local nerve injury, sympathetic nerve fibers regrow more fast resulting in hyperinnervation, but parasympathetic nerve fibers which are key components to initiate and maintain nitric oxide (NO) production and erection status regrow much slower resulting in “autonomic imbalance” (11). In our previous animal experiments of nerve injury-related ED (3,11), some of the novel interventions we investigated such as the low energy shock wave therapy (3,12) and stem cells products (5,13) has been shown to facilitate the local secretion of various neurotrophic factors (NTFs). We speculate that one or more NTFs might be the underlying mechanisms for accelerating nerve regeneration and erectile function recovery in these interventions. However, due to the lack of research of “multicomponent” NTFs, we haven’t found any specific relationships that targeted the erection related nerve regeneration (10).
Glial cell derived neurotrophic factor (GDNF) was one of the up-regulated NTFs associated with these interventions as mentioned above. Tremendous works of literature have shown the vital role of GDNF superfamily in the differentiation, regeneration, and maintaining of pelvic parasympathetic neural networks, especially through the GDNF-GDNF receptor (GFR) α1-Ret pathway and neurturin (NTN)-GFRα2-Ret pathway (14-18). Meanwhile, the nerve growth factor (NGF)-neurotrophic receptor tyrosine kinase type 1 (Ntrk1) pathway has been shown to mainly promote sympathetic regeneration (19). Based on these findings, we hypothesized that GDNF might be beneficial for nerve regeneration especially for parasympathetic nerve regeneration and “correction” of “autonomic imbalance” after cavernous nerve injury. In this project, we tried to test this hypothesis using a specially designed GDNF administration system in an animal model of bilateral cavernous nerve injury (BCNI). In order to create a more stable long-term GDNF enrich local environment, different levels of GDNF were administered locally using an osmotic pump which could deliver GDNF solution continuously and accurately for up to 4 weeks without the need for external connections or frequent handling of animals. Sexual behavior tests and erectile function tests were conducted after treatment. Expression of NTF receptors including GFRs and Ntrk1 were examined and parasympathetic nerve regeneration was investigated. This experiment would give us a preliminary answer of whether precise GDNF enrich local environment is beneficial for the recovery of “autonomic balance” and sexual function after BCNI. We present the following article in accordance with the ARRIVE reporting checklist (available at http://dx.doi.org/10.21037/tau-20-1110).
Experiments were performed under a project license (No.: 201875) granted by institutional ethics board of animal care and use committee of Peking university first hospital, in compliance with national guidelines for the care and use of animals. A total of fifty 8-week-old sexually mature male Sprague-Dawley rats and fifty 12-week-old female Sprague-Dawley rats were used for this study. Rats were kept in 12 h light/12 h dark lighting cycle with food and water freely available. Male rats were randomly grouped into 5 (n=10 each): Sham surgery (Sham), BCNI and placebo treatment, BCNI and 0.1 µg/100 µL GDNF treatment (BCNI+GDNF 0.1), BCNI and 1 µg/100 µL GDNF treatment (BCNI+GDNF 1), BCNI and 10 µg/100 µL GDNF treatment (BCNI+GDNF 10). After 4 weeks of local continuous GDNF release treatment, all male rats underwent unpaced sexual behavior test with female rats and erectile function measurement. The male rats were sacrificed and the blood, serum, peritoneal lavage fluid (PLF), major pelvic ganglion (MPG), urethral tissue, and penile tissue were collected for histology (immunofluorescence staining), laboratory test (ELISA, White blood cell, or WBC count) and molecular studies (Western blot, real time-PCR).
Animal surgery and osmotic pump implantation
To produce BCNI, the rats were weighed and anesthetized with an intraperitoneal injection of pentobarbital sodium. The bladder and prostate were exposed via a midline abdominal incision, and the MPGs and cavernous nerves were identified posterolateral to the prostate. Cavernous nerves were crushed by applying hemostatic forceps (RS-7116, Roboz, Gaithersburg, Germany) for 2 min. The cavernous nerve injury point was 5 mm distal to the MPG. The sham surgery was performed in exactly the same way except no nerves were crushed. Before closing the abdominal wall, an osmotic pump (Alzet micro-osmotic pump, model 1004) filling with specific dose of GDNF (Merck, G1777) was implanted close to the prostate in the pelvic cavity (Figure 1A). GDNF was dissolved in normal saline and was pre-injected in the pump at doses of 0 µg/100 µL, 0.1 µg/100 µL, 1 µg/100 µL, 10 µg/100 µL for rats in groups of BCNI, BCNI+GDNF 0.1, BCNI+GDNF 1, BCNI+GDNF 10 respectively. The osmotic pump should release the GDNF solution locally at a rate around 0.11 µL/hour for up to 28 days.
Unpaced sexual behavior tests
Tests were conducted during the light-on period to provide a behaviorally sluggish baseline condition. Female rats were purchased when the sexual behavior tests were going to be done and they were brought to sexual receptivity via intraperitoneal injection of estradiol benzoate (50 mg/animal) at 48 h and progesterone (0.5 mg/animal) at 10 h before sexual behavior test. Females were kept in the same room and fed with the same food and water as the males. All 10 male rats in each group were put into separate cages (27 cm * 50 cm) 5 min before the start of the test to let them explore the arena before the female was introduced. Each female rat was then randomly paired with a male rat in the same cage. In this unpaced laboratory setting, male rats largely controlled sexual activities because female rats were unable to escape in such a small enclosure, which differed from wild or paced conditions. For each group, the test started at 11.00 AM and ended at 3.00 PM. During the 4 h test, a camera was placed in front of the 10 cages and all activities of the 10 pairs were recorded. The videotapes were viewed and recorded by double-blinded researchers. Four activity types were recorded: chasing, mounting, intromission, and ejaculation. The definitions of sexual behaviors were as follows: Chasing: Pursuit to catch the female, trying to make contact to get the female interested; Mounting: Mounting with pelvic thrusting, but without vaginal penetration; Intromission: Mounting with vaginal penetration, genital licking or grooming after pelvic thrusting; Ejaculation: Presence of repeated deep forward thrust (T+ or T-) after vaginal penetration and/or presence of copulatory plug (P+ or P-) the second day. Ejaculation was judged based on the following rules. T-P-: No repeated deep forward thrust was recorded and no copulatory plug was found (indicating no ejaculation happened); T+P-: Repeated deep forward thrust was recorded but no copulatory plug was found (indicating ejaculation might have happened); T+P+: Repeated deep forward thrust was recorded and copulatory plug was found (indicating ejaculation did happen); T-P+: No repeated deep forward thrust was recorded but copulatory plug was found (indicating early ejaculation might have happened).
Erectile function evaluation
Under anesthesia, the MPG and cavernous nerves of the rat were exposed via a midline laparotomy. The corpora cavernosum of the penis was cannulated with a 25-gauge butterfly needle filled with heparin (250 U/mL) via insertion at the crura. The cannula was connected to a pressure transducer (Biopac 16, CA, USA) for continuous assessment and recording of intracavernous pressure (ICP). Mean arterial pressure (MAP) was recorded continuously as previously described (3,11). The left carotid artery was exposed and separated. A 25-gauge butterfly needle filled with heparin (250 U/mL) was inserted into the carotid artery. The needle was connected to the pressure transducer through a PE-50 tube. The stimulus parameters for cavernous nerve were 1.5 mA, 20 Hz, pulse width 0.2 ms, and duration of 50 s. The maximum increase in ICP for three stimuli per side for each animal was selected for statistical analysis. The rats without successful ICP recording due to technique issues were not involved in the statistical analysis.
Laboratory test of WBC count and GDNF concentration
Blood samples were collected in EDTA prewashed EP tubes for WBC count and regular EP tubes for serum collection. PLF was collected just before the laparotomy procedure during ICP recording as following steps: cut the outer skin of the peritoneum and gently pull it back to expose the inner skin lining the peritoneal cavity; inject 2 mL of normal saline into the peritoneal cavity using a 27-gauge needle; gently massage the peritoneum, insert a 25-gauge needle, bevel up, attached to a 5 mL syringe in the peritoneum and collect the fluid while moving the tip of the needle gently to avoid clogging by the fat tissue or other organs. WBC count in blood and PLF was calculated using an automatic blood analyzer (sysmex XE-2100). GDNF quantification in serum and PLF was measured using enzyme-linked immunosorbent assay (ELISA) kits according to the manufacturer’s protocol (ab213901, Abcam).
Urethral and penile tissue was freshly harvested and fixed and immunofluorescence staining was performed as previously described (3). The primary antibodies included anti-neurofilament (NF; 1:500; ab8135, Abcam), anti-tyrosine hydroxylase (TH; 1:200; AB152, Millipore, Bedford, MA, USA), anti-vesicular acetylcholine transporter (VAChT; 1:200, ABN100, Millipore, Bedford, MA, USA). Secondary antibodies used included Alexa-488– and Alexa-594–conjugated antibodies (1:500; Invitrogen). Smooth muscle in urethral tissue was stained by Alexa-488 conjugated phalloidin (1:400; Invitrogen). Nuclei were stained with 40,6-diamidino-2-phenylindole (DAPI; Invitrogen). Image analysis was performed by computerized densitometry (K pixel number of integrated optical density) using Image-Pro Plus 5.1 (Media Cybernetics, Silver Spring, MD, USA).
Real-time quantitative reverse transcription-PCR
Fresh MPG tissue was immediately homogenized in TRIzol reagent followed by isolation of total RNA. cDNA was synthesized from the RNA using a Super Script III cDNA synthesis kit with random hexamer primers. Expression of the following NTF receptors genes was analyzed: Ntrk1 (GTCTGGTGGGTCAGGGACTA CACACATCACTCTCGGTGCT), GFRα1 (AGCTGCAGCACCAAGTACCGC GCTTGGCCGGAACCTTGTCGAAG), GFRα2 (GCTGTGTGCGGCTGAATCCAAC TATACTCGCTGGGCACACGGTC) and GAPDH (AGGTCGGTGTGAACGGATTTGTGTAGACCATGTAGTTGAGGTCA). Quantitative PCR was performed using the SYBR Green PCR Master kit with an ABI Prism 7500 Sequence Detection System (Applied Biosystems, Foster City, CA, USA).
Protein isolation and Western blot were conducted as previously reported (11). A total of 20 mg protein was loaded for each sample. The primary antibodies used in Western blot were anti-tyrosine hydroxylase (TH, 1:500, AB152, Millipore, Bedford, MA, USA), anti-vesicular acetylcholine transporter (VAChT, 1:500, ABN100, Millipore, Bedford, MA, USA) and β-actin (1:1,000, ab8227; Abcam). After incubation with the secondary antibody, the resulting images were analyzed with ChemiImager 4000 (Alpha Innotech Corp., San Leandro, CA, USA) to determine the integrated density value of each protein band.
Results were analyzed using Prism 5 (GraphPad Software, San Diego, CA, USA) and are expressed as mean ± standard deviations (SD). Multiple groups were compared by using one-way analysis of variance followed by the Tukey Kramer test for post-hoc comparisons (five variables). Statistical significance was set at P<0.05. Numbers analyzed in each group: ejaculation percentage: 10/10; ICP: rats without successful ICP recording were not involved, Sham (8/10), BCNI (7/10), BCNI+GDNF 0.1 (7/10), BCNI+GDNF 1 (8/10), BCNI+GDNF 10 (8/10); Western blot: 6 repeated tests with each sample randomly chosen from the corresponding group; all the other data: 8/10 (randomly chosen from corresponding group).
Influence of local continuous GDNF release on sexual behavior
All rats were healthy and active and no adverse events were recorded. Chasing was the most frequent sexual behavior, especially in the initial stage after the presentation of a female, followed by mounting, intromission, ejaculation in descending order. The average numbers of chasing and mounting were around similar levels among groups (P>0.05) indicating that the libido of male rats was not significantly affected by BCNI or GDNF administration (Figure 1B,C). Intromission was judged according to the duration and observation of genital licking after thrusting. BCNI caused a decrease in the average number of intromissions from 8 times per rat to 4 times per rat (P=0.0064). Local continuous GDNF release treatment increased the average number of intromissions in a dosage dependent manner and significant change happened at the dosage of 10 µg/100 µL with an average number of intromissions recorded at 6.6 times per rat (P=0.029) indicating partial recovery of penile erectile function (Figure 1D). The percentage of rats with confirmed ejaculation (T+P+ and T-P+) was 60% in Sham group. After BCNI, this percentage was 40% with 3/4 of them might be early ejaculation (T-P+). The percentage of confirmed ejaculation (T+P+ and T-P+) in GDNF treated groups are 40–50%, but with lower rates of early ejaculation (T-P+, 10–20%, Figure 1E).
Local continuous GDNF release treatment improves erectile function after BCNI
To further investigate the effect of GDNG on erectile function recovery, erectile hardness was measured by ICP and MAP recording with cavernous nerve stimulation under anesthesia. The sham group exhibited normal ICP curves and high ICP/MAP ratios (0.96±0.19). BCNI consistently resulted in ED with ICP/MAP ratios of 0.47±0.16 (P=0.0002). Recovery of erectile function to varying degrees was observed in the BCNI+GDNF 0.1 (0.49±0.15, P=0.87), BCNI+GDNF 1 (0.63±0.16, P=0.08), BCNI+GDNF 10 (0.78±0.14, P=0.002) groups as reflected by higher ICP/MAP ratios in response to cavernous nerve electrical stimulus compared to the BCNI group (Figure 2, Figure S1).
Osmotic pump implantation induced increased local GDNF concentration and WBC count
In order to investigate the distribution of the administered GDNF. The concentrations of GDNF in serum and PLF were measured (Figure 3A,B). There was no significant difference of GDNF concentration in serum among groups (P>0.05, Figure 3B). The concentrations of GDNF in PLF were significantly higher in BCNI+GDNF 0.1 (8.45±2.88 pg/mL, P=0.02), BCNI+GDNF 1 (9.85±3.53 pg/mL, P=0.01), BCNI+GDNF 10 (12.97±2.59 pg/mL, P=0.0001) groups compared to the Sham group (4.33±0.83 pg/mL). The difference of GDNF concentration in PLF between the BCNI group and the Sham group was not significant (Figure 3A). These results indicated that administered GDNF mainly played its role locally in the peritoneal/pelvic cavity. Any foreign body implantations may cause local or systemic infection or inflammation. Although none of the rats illustrated behavior or gross pathological evidence of infection, we still examined the WBC count locally and systemically. Osmotic pump implantation induced slightly increased WBC counts in PLF about 22–27% compared to the Sham group (P>0.05, Figure 3C) indicating mild local inflammatory response might have happened. The WBC counts in blood were not significantly varied among groups (P>0.05, Figure 3D).
Changes of neurotrophic receptor in MPG influenced by GDNF administration
To explore the influence of GDNF release treatment on the local expression of neurotrophic receptors that are related to the regeneration of the autonomic nervous system, we examined the gene expression level of Ntrk1, GFRα1 and GFRα2 related to GAPDH in MPG using Real-time quantitative reverse transcription-PCR. The expression of Ntrk1 slightly increased after BCNI indicating potential sympathetic over-growth. The administration of GDNF didn’t alter the expression of Ntrk1 significantly (Figure 4A). After BCNI, the gene expression of GFRα1 and GFRα2 are decreased (P<0.05). GDNF administration increased the gene expression of GFRα1 and GFRα2 which suggesting the regeneration of parasympathetic nerve fibers (Figure 4B,C). The expression of GFRα1 was more promoted by GDNF at the BCNI+GDNF 1 group (P=0.0002 compared to BCNI group). Higher level of GDNF (BCNI+GDNF 10) didn’t induce more expression of GFRα1 possibly indicating negative feedback between NTF and receptor. The increased expressions of GFRα2 promoted by GDNF administration however, were in a dose dependent manner (P=0.01 and 0.005 respectively in BCNI+GDNF 1 and BCNI+GDNF 10 groups compared to BCNI group) simply reflecting the increased total amount of parasympathetic nerve fibers in MPG.
Nerve regeneration along the urethra
Cavernous nerve fibers are believed to travel from MPG along the external surface of urethra and join with the internal pudendal nerve at the crus penis to form the dorsal nerve of penis (DNP). In order to examine the nerve rehabilitation of cavernous nerve fibers, urethral tissue was harvested and nerve fibers stained by neurofilament (NF) were examined and compared at different levels (upper 1/3 of urethra and lower 1/3 urethra, Figure 5A,B). The amount changes of NF+ nerve fibers in the upper 1/3 urethra were not significant among groups indicating animals do have some intrinsic nerve regeneration ability. Nerve fibers in lower 1/3 urethra were more influenced by BCNI or GDNF administration indicating various regeneration ability over the longer regrowth route (Figure 5B,C). Nerve injury decreased NF+ nerve fibers, especially at the lower 1/3 urethra (P=0.01). The amount of NF+ nerve fibers at lower 1/3 urethra increased in a dose dependent manner after GDNF administration (P=0.02 in BCNI+GDNF 10 groups compared to the BCNI group).
Regrowth of parasympathetic nerve was promoted by GDNF administration
To investigate the balance of parasympathetic and sympathetic nerve fibers in penile tissue, DNP was examined by the staining of either TH a sympathetic nerve marker or VAChT a parasympathetic nerve marker (Figure 6A). After BCNI, overgrowth of sympathetic nerve or TH+ nerve fibers was robust as previously reported (11). BCNI caused a significant damage to the parasympathetic nerves or VAChT+ nerve fibers that are not fully recovered until 4 weeks later. Local GDNF release treatment promoted the regeneration of parasympathetic nerve fibers in a dose dependent manner. Increased VAChT expression in the treatment groups was further confirmed with Western blot using the protein lysates from penile tissue. The ratio of VAChT expression to TH expression was increased to about 2–3 times in the BCNI+GDNF 1 and BCNI+GDNF 10 groups compared to the BCNI group (P=0.0003 for both, Figure 6B,C). All these data supported the idea that GDNF administration promotes nerve regeneration from MPG, along the urethra, and finally leads to increased nerve fibers especially the parasympathetic nerve fibers in DNP and cavernosum.
In this project, we showed that local continuous GDNF administration was beneficial for the functional and histological recovery of cavernous nerve injury-induced ED. In fact, the whole male sexual response which includes sexual arousal, erection, emission, and ejaculation is precisely orchestrated by multiple levels of neurons (20,21). Sexual arousal is usually stimulated by local tactile sensation or special senses. The complex conversation among cerebral cortex, limbic system, and hypothalamus finally converts into an integrated output that transmits through the spinal cord and parasympathetic nerve fibers to induce NO production and smooth muscle cell relaxation in cavernosum which finally leads to penile erection (Figure 5C) (22,23). Emission and ejaculation which usually follow erection are however mainly controlled by the activity of sympathetic and motor nerves (24). In this project, BCNI animal model was used to mimic the post-prostatectomy nerve injury which usually involves damage to both parasympathetic and sympathetic nerve fibers. Both BCNI and GDNF administration showed no influence on sexual arousal in this sexually mature animal model as the chasing and mounting were comparable among different groups. Analysis of intromission which is an indicator of erectile function however displayed that BCNI significantly impaired erectile function and GDNF administration improved it. This was also confirmed by the results of ICP recording test. Changes in ejaculation showed similar trends as with intromission. The higher percentage of rats with T-P+ (might indicate early ejaculation) in BCNI group however, indirectly reflected the potentially “over-active” sympathetic tone in these rats.
Based on the present results and results from our previous studies (11), parasympathetic nerve fibers regrowth much slower than sympathetic nerve fibers. The latter own robust regeneration ability themselves even without any interventions which often results in sympathetic overgrowth and autonomic imbalance. According to the histological studies, complete or even more sympathetic (TH+) nerve fibers regrowth in DNP could be found 4 weeks after BCNI compared to Sham group. The regeneration of parasympathetic (VAChT+) nerve fibers was significantly impaired after BCNI if no interventions were applied. GDNF as a neurotrophic factor (NTF) was introduced in this study with the expectation to promote autonomic balance recovery during the nerve regeneration process. More MPG originated cavernous nerve fibers nourished by GDNF administration could be found along the urethral tissue. In DNP, the ratio of parasympathetic tone to sympathetic tone was partially recovered by GDNF treatment in a dose dependent manner.
NTF has neural differentiation and neuroprotective effects (25). They themselves hold great therapeutic potential for diseases associated with nerve injury or degeneration (26). Meanwhile, other potential treatment modalities such as the low energy shock wave therapy (3,12) and stem cells products (5,13) have been shown to play their role at least partially through the paracrine of NTFs (5,8). Among all these NTFs, GDNF family consisting of GDNF, neurturin (NTN), artemin (ARTN), and persephin (PSPN) which mainly binds to different GDNF receptors (GFRα1-4) has already been proven to be vital for the differentiation, regeneration, and maintenance of pelvic parasympathetic system (27). In the newborn mice, GFRα1 is mainly expressed by the non-TH nerve fibers (mainly composed of parasympathetic neurons) (28); partially knockdown of GFRα2 has been shown to impair the parasympathetic innervation in the mice penile tissue, but the development of sympathetic network was not affected (14,29); GFR activation might be beneficial for penis-projecting parasympathetic neurons regeneration (30-32) and the expression of GFRα mRNA has been proven to be closely related to the expression of neuronal nitric oxide synthase (nNOS, a marker for a special kind of parasympathetic nerve, some researchers prefer to classify nNOS+ neuron to Non-adrenergic non-cholinergic neuron or NANC neuron, Figure 5C) following BCNI (33). In fact, there are profound changes within MPG after nerve injury. Sprouting axons occurs concurrently with structural or chemical changes raises the possibility of the formation of aberrant synaptic connections resulting in broader effects on the pelvic autonomic circuitry (14). These structural changes are usually accompanied by changes in NTF signaling, such as altered expression of GDNF or GFRs (34,35). In this project, we demonstrated the dynamic changes of Ntrk1, GFRα1, and GFRα2 associated with BCNI and GDNF treatment. The expression of GFRα1 which is the direct receptor for GDNF had a relatively higher expression level at GDNF concentration of 1 µg/100 µL. This could be explained by the overlying manifestation of more parasympathetic regrowth and negative feedback between GDNF and its receptor (less amount of receptor is needed when the NTF concentration is higher). But the precise “inflection point” should be investigated in the future as we only examined 4 different concentrations of GDNF in the present study. The amount of Ntrk1 and GFRα2 however directly reflected the regrowth status of sympathetic or parasympathetic nerves which was corresponding to our histological studies.
One of the obstacles that prevent the use of NTFs in clinical scenario is that rapidly degraded NTFs need to be frequently delivered (36). Although a single injection of NTFs might be able to improve neural survival, this effect did not last for a long time (34). Alternative options of NTFs delivery such as multiple injections (37), more stable dissolved solution (37), viral-mediated or cell-based mediated delivery (38-40) are being extensively studied. The concentration of NTFs is a vital parameter for therapeutic effects and should be calculated precisely (41). In the adult human brain, GDNF is expressed at very low levels (43–70 pg/mg protein at most) (42). The average concentrations of GDNF in cerebrospinal fluid (CSF) and serum are around 218.7 and 711.5 pg/mL respectively in healthy human beings (43). In a previous study by Kim et al. (44), GDNF was infused intracerebroventricularly continuously at a rate of 8.35 ng/0.5 microl/hour (200 ng/day) for 7 days in a rat model of traumatic brain injury, so the GDNF totally administrated was at least 1.4 µg/rat. In another study related to Intracerebroventricularly administration of GDNF, 1–5 µg of GDNF was injected one time into the right lateral cerebral ventricle in a rat model (45). Given the fact that the average volume of CSF in adult SD rats is around 90 µL (46), the administered GDNF concentration is 11.1–55.6 ng/µL in the above mentioned experiments. However, the continuous infusion technique might be superior than the one-time-shot technique due to the short half-life of GDNF. Although hard to measure, rats typically have at least 200 µL peritoneal fluid (47), so the total amount of GDNF administered in our study is around 0.018 to 1.8 pg/mL/d. The average concentrations of GDNF measured in PLF at the end of the experiment did show a dose dependent manner related to the total administrated GDNF amount, however, we did not see any significant differences of GDNF concentrations in serum among groups indicating little permeability of GDNF across bio-membranes under physiological conditions. We assumed that the administrated GDNF mainly played its role locally in the peritoneal or pelvic cavity (40). The continuously released GDNF from osmotic pump bound to the GFRα1 expressed in MPG and cavernous nerve to form a favorable local environment for parasympathetic regeneration for up to 4 weeks which finally resulted in improvements of autonomic balance, erectile function and sexual performance in rats.
Local continuous GDNF delivery technique promotes parasympathetic nerve fiber regeneration, autonomic balance rehabilitation and sexual function recovery in a rat model of BCNI induced ED. The overexpression of Ntrk1 after BCNI is not influenced by GDNF. The expression of GDNF family receptor α1 in MPG is partially promoted by GDNF administration.
Funding: This work was supported by the National Natural Science Foundation of China (No. 81701434).
Reporting Checklist: The authors have completed the ARRIVE reporting checklist. Available at http://dx.doi.org/10.21037/tau-20-1110
Data Sharing Statement: Available at http://dx.doi.org/10.21037/tau-20-1110
Peer Review File: Available at http://dx.doi.org/10.21037/tau-20-1110
Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/tau-20-1110). The authors have no conflicts of interest to declare.
Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved. Experiments were performed under a project license (No.: 201875) granted by institutional ethics board of animal care and use committee of Peking university first hospital, in compliance with national guidelines for the care and use of animals.
Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.
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