Research Article - (2017) Volume 6, Issue 3
Chang Liu1, 2*, Hongtao Jin1, Baodong Yu2, Jinfeng Wei1 and Aiping Wang1
1 Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, PR China
2 Women’s and Children’s Hospital, Qingdao University, Qingdao, PR China
*Corresponding Author:
Chang Liu
Institute of Materia Medica, Chinese
Academy of Medical Sciences & Peking
Union Medical College, Beijing, PR China.
Tel: 86-18553263607
E-mail: lch1001@yeah.net
Received date: May 03, 2017; Accepted date: May 16, 2017; Published date: May 23, 2017
Citation: Liu C, Jin H, Yu B, et al. A 90- day Repeat-Dose Oral Toxicity Study of Yonkenafil Hydrochloride in Beagle Dogs. J Biomedical Sci. 2017, 6:3. doi:10.4172/2254-609X.100067
Yonkenafil hydrochloride, a novel synthetic phosphodiesterase type 5 inhibitor, is a promising drug for the treatment of erectile dysfunction. The repeated-dose toxicity of yonkenafil hydrochloride was assessed in male and female beagle dogs. Twenty-four dogs were randomly allocated to four groups and administered yonkenafil hydrochloride orally at dosages of 0, 7, 30 or 120 mg/kg/day for 90 days followed by a 28-day recovery period. During the test period, clinical signs, mortality, body weight, food consumption, ophthalmoscopy, electrocardiography, hematology, serum biochemistry, urinalysis, organ weights, gross findings and histopathology were examined. There were no abnormal changes in the clinical observations except that gastrointestinal intolerance was observed in the 120 mg/kg/day group. The laboratory and histopathological examinations revealed yonkenafil hydrochloride toxicity to various organs, including the thyroid gland, liver, prostate, uterus and breast; at the end of the recovery period, this damage was resolved. The level of yonkenafil hydrochloride that resulted in no observable adverse effects in beagle dogs was 7 mg/kg/day.
Keywords
Yonkenafil hydrochloride; Erectile dysfunction; Toxicity; Clinical signs
Introduction
According to the definition of the National Institutes of Health Consensus Development Conference on Impotence, erectile dysfunction (ED), which will affect the lives of approximately 300 million men worldwide by the year 2025, is the inability to achieve or maintain an erection sufficient for satisfactory sexual performance [1,2]. Pharmacotherapy is currently the mainstay treatment for ED. According to the suggestion of the American Urological Association (AUA) guideline on ED, the first-line treatment of ED should be phosphodiesterase type 5 (PDE5) inhibitors, which include sildenafil, tadalafil and vardenafil [3]. Treatment of ED with PDE5 inhibitors is generally well tolerated, although some side effects, such as headache, flushing, dyspepsia, nasal congestion and unusual visual disturbances, have been reported [4,5]. PDE5 inhibitors are structurally similar to cGMP and compete with cGMP at the catalytic site of PDE5. Inhibition of PDE5 in human corpus cavernosum increases intracellular cGMP levels in trabecular smooth muscle cells to achieve relaxation and increased blood flow to the penis [6-9]. Recent studies have shown that PDE5 inhibitors have remarkable therapeutic effects on many other diseases, such as benign prostatic hyperplasia, pulmonary hypertension, and Alzheimer’s disease [10-12].
With the widespread success and acceptance of these agents, major interest was generated in the potential of PDE5 inhibitors. Several new PDE5 inhibitors, such as avanafil, udenafil, SLx-2101 and mirodenafil, are candidates to enter the market in coming years [13]. Yonkenafil hydrochloride, a novel synthetic PDE5 inhibitor and analog of sildenafil, is a promising drug for the treatment of ED. Yonkenafil (IC50=2.0 nM) is pharmacologically more active than sildenafil (IC50=4.5 nM) and possesses fewer gastrointestinal side effects [14]. Previous research has also demonstrated that yonkenafil can efficiently reduce cerebral infarction, neurologic deficits, edema, and neuron damage in the infarct area [14,15], and suppress the microglial activation to promote neuronal survival [16,17]. Yonkenafil has been submitted to China Food Drug Administration (CFDA) for the approval as a new drug, and is now undergoing clinical trials in China [18].
However, the information regarding the toxicity of yonkenafil is very limited. An understanding of the safety profile of yonkenafil is imperative to fully anticipate its therapeutic potential. This study was designed to evaluate the repeated-dose toxicity of yonkenafil hydrochloride in beagle dogs, with the purpose of obtaining information on the safety of yonkenafil hydrochloride. The study was performed according to “the Guidelines for Longterm Toxicity Tests of Chemicals” provided by the China Food and Drug Administration (CFDA) under Good Laboratory Practice Regulations. This study was conducted in accordance with the principles and procedures outlined in the National Institutes of Health Guide for the Care and Use of Laboratory Animals. This protocol was approved by The Animal Care &Welfare Committee Institute of Materia Medica, CAMS&PUMC.
Materials and Methods
Test article
Yonkenafil hydrochloride (Figure 1) (purity 99.40%) is a watersoluble, odorless, yellow powder. The capsules (300-500 mg, 200-300 mg, 40-50 mg yonkenafil hydrochloride/capsule) were obtained from Tianjin Tasly Company Ltd. (Tianjin, P.R. China) and were used for oral administration in this study. The number of capsules for each dog was calculated every week based on the recent body weight.
Figure 1: The structure of yonkenafil hydrochloride. Yonkenafil hydrochloride (2-(2-ethoxy-5-(4- ethylpiperazin-1-yl sulfonyl) phenyl)-5-methyl-7-propyl-3H-pyrrolo[2, 3-d] pyrimidin -4(7H) -one- hydrochloride). Formula: C24H33N5O4S·HCl, MW: 523.67.
Animals and husbandry
Thirty-two healthy male and female Beagle dogs weighing 6-8 kg and aged 6-12 months were obtained from the Institute of Laboratory Animal Science, Peking Union Medical College & Chinese Academy of Medical Sciences (Beijing, China). All dogs were acclimatized in the experimental facilities for a period of 4 weeks before the onset of the experiment. The animals were housed individually in cages and maintained in an environmentally controlled animal room. The animal room was monitored and maintained under a 12 h light-dark cycle controlled via an automatic timer with a temperature of 23 ± 5°C and relative humidity between 40% and 60%. The ventilation frequency was 15 times h-1 throughout this study. The dogs were provided ad libitum access to Certified Expanded Diet (Laboratory Animal Science Center, Academy of Military Medical Sciences, Beijing, China). Municipal water, processed through a reverse osmosis membrane, was provided to the dogs ad libitum.
Study design and dose selection
Male and female dogs (n=4/sex/dose) were assigned randomly into four treatment groups (0, 7, 30 and 120 mg/kg/day yonkenafil hydrochloride). Two animals per sex per group were sacrificed under pentobarbital anesthesia at the end of the treatment period on Day 90, and the remaining two animals per sex per group were examined after a 28-day recovery period.
The selection of dosage levels in the current study was based on the results of an acute toxicity study of yonkenafil hydrochloride in mice and pharmacodynamic data from rats. In the acute study, the LD50 was 2000 mg/kg/day, and the 95% confidence interval was from 1610 to 2438 mg/kg/day. In the pharmacodynamic study, the minimal effective dose was 6 mg/kg/day and the maximal effective dose was 24 mg/kg/day. The optimal dose was 12 mg/kg/day. In the present study, 120 mg/kg/day was specified as the high-dose level, which was 33.3 times the optimal effective dosage. Lower doses of 30 mg/kg/day and 7 mg/kg/day were selected as mid- and low-dose levels, respectively.
Clinical observation
Mortality and clinical observations were recorded daily. The body weights and temperatures of all animals were measured twice during the quarantine period, and once every week during the administration and recovery periods. Food consumption was measured twice during the quarantine period and at weekly intervals during treatment and convalescence. The amounts of food (approximately 300 g) were recorded before they were supplied to each cage, and the remaining food was measured the next day to determine the differences, which were regarded as daily food consumption (g per 100 g bodyweight).
Ophthalmoscopic examinations were performed on each dog before the start of treatment (Day -14, Day -7, i.e., 14 and 7 days before treatment initiation, respectively), during the treatment period (Day 45), after the last dose (Day 90) and after recovery (Day 118) using a binocular indirect ophthalmoscope (Topcon, Japan). The observation areas included the cornea, conjunctiva, sclera, iris, lens and fundus. Electrocardiograms were conducted on Day-14, Day-7, Day 45, Day 90 and Day 118 to measure the heart rate, P-R interval, QRS interval and QT interval.
Laboratory testing parameters
Blood samples were collected from all animals on Day-14, Day- 7, Day 45, Day 90 and Day 118. Urine samples were collected from all animals on Day 90 and Day 118. All dogs were fasted for more than 12 h prior to the blood/urine sample obtained. Blood samples were drawn from a forelimb vein into evacuated blood collection tubes. Under anesthesia, urine was collected from the bladder onto a specimen test paper through a catheter. EDTA and sodium citrate were used as anticoagulants for the blood coagulation study.
Hematology and blood coagulation
The hematological parameters were assessed using a MEK- 6318K Automated Hematology Analyzer (Nihon-Kodhen Co., Tokyo, Japan) for erythrocyte counts (RBC), hemoglobin (Hb), hematocrit (HCT), mean corpuscular volume (MCV), mean corpuscular hemoglobin (MCH), mean corpuscular hemoglobin concentration (MCHC), red cell distribution width-variation coefficient (RDW-CV), platelet count (PL), mean platelet volume (MPV), platelet distribution width (PDW), plateletcrit (PCT), leukocyte counts (WBC) and differential cell count (DC). Blood smears were stained with Wright-Giemsa brilliant-cresyl-blue (Heath and Daland, 1931), and the reticulocyte count (Reti) was performed via light microscopy.
The coagulation parameters, including thrombin time (TT), prothrombin time (PT), activated partial thromboplastin time (APTT), and ? brinogen (Fbg), were evaluated with the DIAGNOSTICA STAGO STA-4 Coagmaster kit (Junior Instruments Co., Gennevilliers, France).
Serum biochemistry
The blood chemistry parameters were determined using a Vitalab Autoanalyzer (Vital Scienti?c, Dieren, the Netherlands) and an AVL-9181 Autoelectrolyte Analyzer (AVL Scienti?c Co., Roswell, Georgia, USA). The parameters measured were aspartate aminotransferase (AST), alanine aminotransferase (ALT), alkaline phosphatase (ALP), glucose (GLU), blood urea nitrogen (BUN), uric acid (UA), lactate dehydrogenase (LDH), total protein (TP), albumin (ALB), total bilirubin (T-BIL), total cholesterol (T-CHO), triglycerides (TG), creatinine (CRE), creatine kinase (CK), albumin– globulin ratio (A/G), and serum levels of calcium (Ca), sodium (Na), potassium (K), and chloride (Cl).
Urinalysis
Urinalysis was conducted using Multistrix® Strips (Bayer Corp., Bridgend, South Wales, UK) for parameters including glucose (GLU), bilirubin (BIL), ketones (KET), speci?c gravity (SG), occult blood (BLO), pH, protein (PRO), urobilinogen (URO), nitrites (NIT), leukocytes (LEU) and urinary sediment.
Necropsy and histopathologic examination
2 dogs/sex/group were sacrificed under ether anesthesia at the end of the treatment period, and the remaining two dogs/ sex/group were sacrificed at the end of the recovery period. A thorough necropsy was performed, and the following organs were excised and weighed: brain, lungs, heart, liver, spleen, thymus, kidneys, adrenal glands, prostate, testes, epididymitis, uterus and ovaries. The relative weight (weight per 100 g body weight) of each organ was calculated and recorded. The above organs and the thyroid gland, parathyroid glands, salivary glands, gall bladder, pancreas, sternum and bone marrow, spinal cord, pituitary gland, esophagus, stomach, intestines (duodenum, jejunum, ileum and colon), lymph nodes (mesenteric), urinary bladder, breast, trachea, sciatic nerve and optic nerve were ? xed in 10% buffered formalin solution. These samples were routinely processed, embedded in paraffin, sectioned at 5 μm, and stained with hematoxylin-eosin for histopathological examination.
Toxicokinetics
A concomitant toxicokinetics (TK) study was performed in the yonkenafil hydrochloride-treated groups. An Agilent 1100 series HPLC system (Agilent Technologies, Palo Alto, CA, USA) coupled to an Applied Biosystems Sciex Q-trap™ mass spectrometer (Concord, Ontario, Canada) via an electrospray ionization (ESI) source was used for analysis. Applied Biosystems Analyst software package version 1.3.2 was used to control the LC-MS/ MS system and for data acquisition and processing. Yonkenafil hydrochloride and the I.S. (internal standard) (diazepam 250 ng/ mL) were separated on a 5 μm Zorbax Extend C18 column (150 × 4.6 mm I.D. from Agilent Technologies) maintained at 30°C. The mobile phase consisted of 85% methanol and 15% 10 mM ammonium acetate buffer delivered at a flow rate of 1.0 mL/min. A two-phase switching valve was used to divert the pre-eluent from entering the ion source. An approximately 1:1 split of the column eluent was included so that only 0.5 mL/min entered the mass spectrometer. The mass spectrometer was operated in the positive ESI mode with multiple reaction monitoring (MRM) at unit resolution. Nitrogen was used as the nebulizer, heater, curtain gas and collision activation dissociation (CAD) gas. The precursorto- product ion transitions were monitored at m/z 488.4→ 99.2 and m/z 488.1→ 310.1 for yonkenafil hydrochloride and at m/z 285.2→m/z 193.2 for diazepam. The mass spectrometer instrumental parameters were tuned to maximize the generation of precursor and fragment ions by infusion of a solution of yonkenafil hydrochloride and I.S. into the ESI source at 10 μL/min. The optimum parameters were as follows: nebulizer (GS1), heater (GS2) and curtain gas flow rates: 55, 40 and 15 units, respectively; ion spray needle voltage: 1500 V; heater gas temperature: 450°C; collision gas: (N2) medium; declustering potential: 85 V; collision energies: 83 eV (m/z 488.4→ 99.2) and 39 eV (m/z 488.4→ 310.3) for yonkenafil and 44 eV for diazepam.
Blood samples were obtained on the 1st day (0.5, 1, 2, 3, 4, 5, 6, 7, 8, 24 h after dosing), 45th day (0.5, 5, 24 h after dosing), 90th day (0.5, 5, 24, 48, 72, 96 h after dosing) and 118th day for plasma yonkenafil hydrochloride level determinations. On each occasion, approximately 2.0 mL of blood was drawn from the foreleg vein of the dogs; the samples were collected in tubes containing heparin. The blood samples were centrifuged immediately, and the plasma samples were stored in a -20°C freezer until analysis. After thawing at room temperature, the plasma samples were vortexed and an aliquot (100 μL) was mixed with 100 μL I.S. (internal standard) (diazepam 250 ng/mL) and 100 μL methanol:water (50:50, v/v) and 50 μL NaOH (1 M) in a 10 mL capped tube. The mixture was vortexed for 10 s and was extracted with 3.0 mL diethylether:dichloromethane, 60:40, v/v).
After shaking for 10 min and centrifuging at 3500 × g for 5 min, the upper organic phase was carefully transferred to another tube and evaporated at 40°C under a gentle stream of nitrogen. The residue was reconstituted in 200 μL mobile phase, and 20 μL was injected into the LC-MS/MS system. TK determination was conducted at the College of Life Science of Jilin University (Changchun, China).
Statistical analysis
The experimental groups were compared against the control group in terms of body weight, food consumption, hematological parameters (except for the differential leukocyte count and reticulocyte count), blood chemistry values, and organ weights. If the data were homogenous according to Bartlett’s test, a oneway analysis of variance (ANOVA) was used. If the data were not homogeneous (and for the differential leukocyte count and reticulocyte count), Kruskal-Wallis’s test was employed. The parameters found to be significant in the one-way analysis of variance (ANOVA) were assessed by the Dunnett test. Percentage and ratio data from the urinalysis were evaluated by chi-square tests. Significance levels for pair-wise comparisons were reported at p<0.05 or p<0.01.
Results
Clinical observations
All beagle dogs survived until the scheduled necropsy. In 120 mg/kg/day group, emesis occurred 2-5 h after yonkenafil hydrochloride administration in three dogs (one male and two females) on Day 1. One male dog in the 120 mg/kg/day group became emaciated after Day 17, and penile erection was observed frequently. Polysialia and soft feces were observed in three dogs in the high-dose group after Day 20, and these symptoms disappeared a few days later. No other abnormal clinical signs were observed in other groups (Table 1).
| Findings | Males | Females | ||||||
| Control | Low | Medium | High | Control | Low | Medium | High | |
| (n=4) | (n=4) | (n=4) | (n=4) | (n=4) | (n=4) | (n=4) | (n=4) | |
| Emesis | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 2 |
| Emaciation | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 0 |
| Polysialia and soft feces | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 2 |
Table 1: Effect of yonkenafil hydrochloride on clinical symptoms in beagle dogs during the 90-day study.
Group mean body weight was statistically significantly decreased after 6 and 13 weeks of dosing in the male dogs in the high-dose group compared with the control group (decreases of 24% and 34%, respectively). However, these changes were not observed in female dogs. The weight changes are presented in Figures 2 and 3. The mean daily food consumption was comparable between the control and treatment groups in both genders. There was no significant change in body temperature, and the numerical values of their temperatures were in the normal range. Increases in eye discharge were observed in the 120 mg/kg/day group during the treatment period; however, these symptoms resolved by the end of recovery. The electrocardiographic examination (heart rate, P-R interval, QRS interval, QT interval) did not indicate any treatment-related adverse effects
Figure 2: Effect of yonkenafil hydrochloride on the body weight of male dogs during the 90-day toxicity study. All data are mean ± SD (3 dogs/group/sex). *p?0.05.
Figure 3: Effect of yonkenafil hydrochloride on the body weight of female dogs during the 90-day toxicity study. All data are mean ± SD (3 dogs/group/sex).
Laboratory Investigations
Hematology and coagulation
On Days 45 and 90, there were no statistically significant differences in any of the hematology parameters between any of the treatment groups and the control group for either sex. Fibrinogen levels were statistically significantly increased in the male dogs at the 7 and 30 mg/kg/day doses on Day 90 compared to the control group (Table 2). The significance was, however, due to the low value in the control group and, therefore, was not considered treatment-related. In addition, the Fbg values at the 7 and 30 mg/kg/day doses were comparable to pretest and Day 45 values.
| Dose | Male | ||||||
| (mg/kg/day) | ALB(g/L) | CK(U/L) | LDH(U/L) | A/G | AST (U/L) | Fbg (mg/dl) | |
| D -7a | 0 | 32.3±0.9 | 352.0±75.4 | 153.7±66.5 | 1.04±0.11 | 36.3±5.1 | 272.3±32.5 |
| 7 | 32.1±1.9 | 396.7±63.9 | 112.3±16.6 | 1.09±0.06 | 40.0±8.5 | 262.0±87.1 | |
| 30 | 32.6±1.1 | 445.7±78.7 | 195.7±61.7 | 1.08±0.05 | 42.7±4.9 | 268.5±18.6 | |
| 120 | 32.2±0.3 | 467.7±59.2 | 166.7±63.7 | 1.09±0.15 | 41.0±1.0 | 316.3±39.7 | |
| D 45a | 0 | 34.8±0.7 | 327.0±82.1 | 149.7±21.2 | 1.18±0.08 | 34.3±1.52 | 233.3±23.9 |
| 7 | 32.8±0.8 | 331.7±68.4 | 111.0±31.1 | 1.12±0.02 | 40.3±12.7 | 251.3±30.8 | |
| 30 | 33.4±1.0 | 369.7±40.3 | 175.3±27.5 | 1.13±0.08 | 39.7±1.2* | 266.6±31.6 | |
| 120 | 30.5±2.6 | 458.0±94.4 | 286.3±128.4 | 0.92±0.17 | 41.3±7.2 | 238.9±28.8 | |
| D 90a | 0 | 34.7±1.7 | 244.3±36.9 | 114.0±11.3 | 1.19±0.04 | 35.0±2.0 | 165.4±20.7 |
| 7 | 33.30±1.11 | 233.0±50.9 | 77.7±25.4 | 1.27±0.04 | 41.0±7.0 | 260.1±48.3* | |
| 30 | 33.2±1.2 | 298.7±59.0 | 131.3±36.1 | 1.06±0.08 | 45.7±5.7* | 260.4±16.0* | |
| 120 | 27.5±3.6* | 561.3±41.9** | 386.0±53.4** | 0.88±0.14* | 82.7±27.2** | 324.6±59.1* | |
| D 118b | 0 | 32.1 | 189 | 63 | 1.05 | 28 | 236.1 |
| 7 | 32.3 | 267 | 77 | 0.99 | 50 | 211.6 | |
| 30 | 31.3 | 205 | 67 | 0.92 | 44 | 208.2 | |
| 120 | 27.9 | 222 | 97 | 0.9 | 33 | 278.8 |
Table 2: Selected laboratory parameters of male dogs after 90-day administration of yonkenafil hydrochloride and 28-day recovery.
Serum biochemistry
Blood chemistry tests revealed no statistical differences between the groups before treatment initiation. On Day 45, the GLU value of male beagles slightly increased at 7 and 30 mg/kg/day groups (4.76 ± 0.73 and 4.63 ± 0.13, respectively) compared with the value at 0 mg/kg/day group (3.31 ± 0.11). Increased GLU values at 7 and 30 mg/kg/day groups were also found on Day 90(4.79 ± 0.41, 4.10 ± 0.11 and 3.26 ± 0.08, for low-, mid- and control group, respectively). However, these minor changes were within the normal ranges. Decreased ALB and A/G and increased CK, AST and LDH at 120 mg/kg/day male beagles were observed on Day 90, and these parameters returned to normal at the end of the recovery period (Tables 2 and 3). No other abnormal findings were observed.
| Dose | Female | ||||||
| (mg/kg/ day) |
ALB(g/L) | CK(U/L) | LDH(U/L) | A/G | AST(U/L) | Fbg (mg/dl) | |
| D -7 a | 0 | 33.4±1.4 | 377.7±125.9 | 158.3±48.2 | 1.03±0.13 | 41.3±2.1 | 275.4±66.1 |
| 7 | 35.4±1.9 | 279.3±83.1 | 101.3±30.5 | 1.18±0.09 | 40.7±8.0 | 248.9±27.5 | |
| 30 | 33.9±1.3 | 399.0±125.0 | 123.3±42.7 | 1.13±0.14 | 40.3±8.5 | 249.8±19.0 | |
| 120 | 34.6±1.8 | 296.0±86.6 | 119.3±25.7 | 1.19±0.04 | 40.7±6.0 | 250.3±30.9 | |
| D 45 a | 0 | 32.6±3.8 | 369.7±130.0 | 211.0±102.6 | 1.06±0.26 | 39.0±9.5 | 231.6±24.1 |
| 7 | 34.5±0.6 | 231.0±79.8 | 100.3±29.7 | 1.17±0.03 | 41.0±11.8 | 244.4±48.9 | |
| 30 | 33.4±0.7 | 333.0±66.57 | 152.3±41.5 | 1.09±0.11 | 36.3±4.0 | 268.5±62.8 | |
| 120 | 32.9±1.0 | 271.0±123.0 | 133.0±49.3 | 1.05±0.14 | 34.00±11.3 | 273.2±59.1 | |
| D 90 a | 0 | 34.2±1.00 | 260.0±103.1 | 102.3±19.1 | 1.26±0.09 | 36.7±10.2 | 238.6±32.7 |
| 7 | 34.3±1.7 | 182.67±17.6 | 70.7±22.3 | 1.87±0.19 | 42.0±7.9 | 272.8±56.8 | |
| 30 | 33.2±2.1 | 225.0±21.0 | 97.3±20.6 | 1.09±0.13 | 34.7±5.5 | 244.7±39.1 | |
| 120 | 30.7±2.7 | 331.7±128.1 | 130.0±41.7 | 1.00±0.19 | 38.7±12.1 | 305.8±85.9 | |
| D 118 b | 0 | 30.8 | 155 | 52 | 1.01 | 22 | 186.9 |
| 7 | 33.4 | 166 | 37 | 1.19 | 36 | 228.6 | |
| 30 | 33.3 | 183 | 79 | 1.08 | 34 | 217.2 | |
| 120 | 30.6 | 126 | 54 | 1.03 | 26 | 195.8 |
a) Values are presented as means±SD. The number of animals in each group was 4/sex for 90-day treatment period.
b) The number of animals in each group was 2/sex for 28-day recovery period.
Table 3: Selected laboratory parameters of female dogs after 90-day administration of yonkenafil hydrochloride and 28-day recovery.
Urinalysis
On Day 90 and Day 118, the indexes of PRO, BIL and KET were positive in all yonkenafil hydrochloride groups (data not shown). The changes observed in the urinalysis could not be definitively declared as indicating yonkenafil hydrochloride-related toxicity.
Organ weights
The selected absolute organ weight and organ-to-terminal body weight ratio (relative organ weight) are summarized in Table 4. At the end of dosing, the absolute and relative uterus weights were increased in females at 7, 30 and 120 mg/kg/day compared with the control group. The absolute and relative liver weights were increased in males at the high dose. Decreased absolute prostate weight was observed in the high-dose group. At the end of recovery, there were no notable differences in absolute and relative organ weights in either males or females.
| Organ | Time | Detection item | 0 mg/kg/day | 7 mg/kg/day | 30 mg/kg/day | 120 mg/kg/day | |
| Male | Liver | D90 a | AW | 248.23 | 269.85 | 244.31 | 277.55 |
| D118 b | 285.31 | 235.39 | 264.66 | 245.04 | |||
| D90 a | RW | 2 | 2.4 | 2.2 | 3.5 | ||
| D118 b | 2.6 | 2 | 2 | 2.6 | |||
| Prostate | D118 b | AW | 6.28 | 7.73 | 3.74 | 2.61 | |
| D 90 a | 4.25 | 4.91 | 5.3 | 4.24 | |||
| D118 b | RW | 0.03 | 0.03 | 0.03 | 0.03 | ||
| D118 b | 0.04 | 0.04 | 0.04 | 0.05 | |||
| Female | Liver | D90 a | AW | 215.32 | 223.58 | 212.39 | 224.75 |
| D118 b | 208.47 | 177.83 | 191.96 | 201.33 | |||
| D 90 a | RW | 2.4 | 2.3 | 2.1 | 2.7 | ||
| D118 b | 2.6 | 2.3 | 2.8 | 2.5 | |||
| Uterus | D90 a | AW | 2.03 | 14 | 11.16 | 8.26 | |
| D118 b | 5.66 | 3.2 | 1.38 | 3.33 | |||
| D 90 a | RW | 0.02 | 0.25 | 0.12 | 0.12 | ||
| D118 b | 0.06 | 0.04 | 0.02 | 0.04 |
a) Values are presented as means. The number of animals in each group was 2/sex for 90-day treatment period.
b) The number of animals in each group was 2/sex for 28-day recovery period.
Table 4: Selected absolute organ weights (AW) and relative organ weights (RW) of dogs after 90 days of administration of yonkenafil hydrochloride and 28-day recovery.
Pathology
Gross examination
During necropsy after the last dose, hematomas were found at the edge of the spleen in dogs in the control and low-dose groups. In one female dog, one ovary was atrophied in the 120 mg/kg/ day group. In the 120 mg/kg/day group, a goiter was found in two male dogs. At the end of recovery, the dogs examined showed no abnormalities (Table 5).
| Organ | Findings | Males | Females | ||||||
| Control | Low | Medium | High | Control | Low | Medium | High | ||
| (n=2) | (n=2) | (n=2) | (n=2) | (n=2) | (n=2) | (n=2) | (n=2) | ||
| Thyroid gland | Goiter | 0 | 0 | 0 | 2 | 0 | 0 | 0 | 0 |
| Spleen | Hematoma | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| Ovary | Atrophy | - | - | - | - | 0 | 0 | 0 | 1 |
Table 5: Summary of gross findings after a 90-day oral administration of 7, 30 or 120 mg/kg/day to beagle dogs.
Histopathological examination
After the treatment period, hematomas at the edge of the spleen and parafollicular hyperplasia of the thyroid gland were found in the control group. Parafollicular hyperplasia was also seen in the 7 and 30 mg/kg/day groups. In the 120 mg/kg/day yonkenafil hydrochloride group, hepatic steatosis, parafollicular hyperplasia, endometrial hyperplasia, hyperplasia of mammary glands and acinar epithelial degeneration of the prostate were observed (Table 6). At the end of recovery, a hematoma was found at the edge of the spleen in one dog in the 0 mg/kg/day group. In the 120 mg/kg/day group, degenerative changes in the prostate and hyperplasia of the mammary glands were also observed, but the pathological lesions were partially alleviated. No abnormal changes were found in other groups (Table 7).
| Organ | Findings | Males | Females | ||||||
| Control | Low | Medium | High | Control | Low | Medium | High | ||
| (n=2) | (n=2) | (n=2) | (n=2) | (n=2) | (n=2) | (n=2) | (n=2) | ||
| Spleen | Hematoma | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |
| Thyroid gland | Parafollicular hyperplasia | 1 | 1 | 1 | 2 | 0 | 0 | 0 | 0 |
| Liver | Hepatic steatosis | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 0 |
| Uterus | Endometrial hyperplasia | - | - | - | - | 0 | 0 | 0 | 2 |
| Mammary gland | Hyperplasia | - | - | - | - | 0 | 0 | 0 | 2 |
| Prostate | Epithelial degenerative changes | 0 | 0 | 0 | 2 | - | - | - | - |
Table 6: Summary of histopathological findings after a 90-day oral administration of 7, 30 or 120 mg/kg/day to beagle dogs.
| Organ | Findings | Males | Females | ||||||
| Control | Low | Medium | High | Control | Low | Medium | High | ||
| (n=2) | (n=2) | (n=2) | (n=2) | (n=2) | (n=2) | (n=2) | (n=2) | ||
| Spleen | Hematoma | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 |
| Thyroid gland | Parafollicular hyperplasia | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |
| Liver | Hepatic steatosis | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |
| Uterus | Endometrial hyperplasia | - | - | - | - | 0 | 0 | 0 | 0 |
| Mammary gland | Hyperplasia | - | - | - | - | 0 | 0 | 0 | 1 |
| Prostate | Epithelial degenerative changes | 0 | 0 | 0 | 1 | - | - | - | - |
Table 7: Summary of histopathological findings after a 28-day recovery period.
Toxicokinetics
Systemic exposure in beagle dogs was indicated by the plasma AUC0-t and Cmax. There were significant differences in the pharmacokinetic parameters of yonkenafil hydrochloride between males and females during the 90-day oral administration for the mid- and high-dose groups. The AUC0-t, AUC0-∞ and Cmax were much lower in females than in males. The plasma concentration of yonkenafil hydrochloride on the Day 1, Day 45 and Day 90 demonstrated a dose-dependent and linear increase (r>0.798, p<0.01) with maximum plasma values observed at approximately 2 hr after administration. No significant accumulation of exposure level was observed after 45 or 90 days of administration. No plasma concentration of yonkenafil hydrochloride was detected after the 28-day recovery period.
Discussion
Since sildenafil’s approval by the US Food and Drug Administration (FDA) in March 1998, the concept of PDE5 inhibitors for the treatment of ED has gained tremendous interest [19]. Yonkenafil hydrochloride, a novel synthetic PDE5 inhibitor that is structurally similar to cGMP, has been evaluated for its potential clinical use for ED. As part of a non-clinical safety program to evaluate yonkenafil hydrochloride, the current study was conducted to assess the potential repeated-dose toxicity of yonkenafil hydrochloride in beagle dogs.
In this 90-day oral toxicity study conducted with male and female beagles, all treated and control animals survived the experimental period in good general health. The mean body weights and body weight gain of the treated male dogs in the 120 mg/kg/day group significantly decreased compared with the control group. By contrast, the body weight and body weight gain of females were comparable to the controls throughout the experiment. No significant changes in food intake were observed in male or female dogs or among treatment groups. In the absence of other observations associated with systemic toxicity and lower feed intake, the magnitude of the body weight decrease in the highdose group males compared with the controls exceeded 34% at Day 90. This finding might indicate that the dogs challenged with the high drug dose reached or exceeded the maximum tolerated dose.
At the high dose (120 mg/kg/day), emesis, emaciation, transient salivation and soft feces were observed in a few dogs, and these symptoms disappeared a few days later. These results indicate that yonkenafil hydrochloride induced gastrointestinal intolerance at the high dose. We did not observe gastrointestinal pathological changes in the histopathological examination. Thus, the effect of yonkenafil hydrochloride in the gastrointestinal tract is at the functional level. Similarly, gastrointestinal intolerance was observed in dogs that received sildenafil in 1-month and 6-month preclinical studies [20].
Significant differences were observed in the results of the biochemical parameters of male dogs in the 120 mg/kg/day dose group. Lower ALB and A/G and higher AST, LDH were observed on Day 90 in males in the high-dose group compared with the control group. Moreover, increased absolute and relative liver weights and the finding of hepatic steatosis were observed in the high dose yonkenafil hydrochloride-treated males. These changes may indicate that hepatic toxicity is caused by yonkenafil hydrochloride. After the 28-day recovery period, all of these changes returned to normal, demonstrating that the hepatic toxicity caused by a high dose of yonkenafil hydrochloride is reversible.
According to the coagulation test, an increase in fibrinogen was found in all yonkenafil hydrochloride-treated groups on Day 90, and the parameter returned to normal after the recovery period. Because this change was within the normal historical range of the laboratory, we did not consider this parameter to be related to yonkenafil hydrochloride toxicity.
Organ weight changes have long been considered a sensitive marker of chemically induced organ damage [21]. In the present study, elevated absolute and relative uterus weights were observed in all yonkenafil-treated groups. In the histopathological examination, endometrial hyperplasia of the uterus was observed in the high-dose group. Although the changes resolved after the recovery period, these findings suggest that this drug might affect the uterus after long-term treatment. Meanwhile, decreased absolute prostate weights were found in the highdose group. Combined with the finding of degenerative change in the prostate in histopathological examination, we concluded that the prostate was also a target organ for toxicity.
In the gross examination, hematomas were found at the edge of the spleen in dogs in the 0 and 7 mg/kg/day groups. Additionally, in the histopathological examination on Day 90, the change was only found in one dog in control group, and another one dog in control group was also observed hematoma in spleen after 28- day recovery period. We considered this change was due to the artifact of the necropsy procedure.
At the end of the treatment period, hepatic steatosis, parafollicular hyperplasia, endometrial hyperplasia of the uterus, hyperplasia of the mammary glands and degenerative changes in the prostate were observed in the high-dose group. Because parafollicular hyperplasia was also found in the control group, further clarification is required to determine whether the thyroid changes were induced by yonkenafil hydrochloride. At the end of recovery, no abnormal histopathological findings were observed in the liver, thyroid gland or uterus. Although degenerative changes in the prostate and hyperplasia of the mammary glands were found in the high-dose group, the degree and range of the pathological lesions were alleviated, indicating the reversibility of toxicity.
From the results in this study and in previous reports, we conclude that there are both differences and similarities between the toxicity of yonkenafil hydrochloride and other PDE5 inhibitors. Species-specific effects of sildenafil in dogs (beagle pain syndrome, male dogs), mice (marked intestinal dilatation) and rats (adaptive reversible hepatocellular hypertrophy associated with secondary thyroid hypertrophy) were found in a few longterm studies [20]. The most common adverse effects of sildenafil and yonkenafil in beagle dogs were GI intolerance, such as emesis and transient salivation. Hepatic steatosis and parafollicular hyperplasia of the thyroid were also observed in yonkenafiltreated male dogs. Further study is needed to explain whether there is a relationship between hepatic steatosis and thyroid hypertrophy induced by yonkenafil hydrochloride. Additionally, yonkenafil hydrochloride may affect reproductive organs such as the prostate, uterus and breast. However, these changes were resolved or attenuated after a 28-day recovery period. The reasons for the differences between yonkenafil hydrochloride and other PDE5 inhibitors remain unknown, and further research concerning the mechanisms is needed.
Under the conditions of our study, the animals in the 120 mg/ kg/day yonkenafil hydrochloride group demonstrated toxic effects on the target organs, including the thyroid gland, liver, prostate, uterus and breast. It is notable that these effects (except damage to the uterus and breast) were only observed in male dogs. According to the toxicokinetic results, these differences may due to gender differences in drug metabolism. Other PDE5 inhibitors, such as sildenafil, vardenafil and avanafil, undergo hepatic metabolism via the CYP3A4 pathway, but no gender difference was reported [21-23]. Thus, further research is needed concerning the mechanism of action and metabolism of yonkenafil hydrochloride. Most of the changes caused by yonkenafil hydrochloride were resolved or attenuated by the end of the recovery period, suggesting that the damage to these organs is reversible.
Based on the adverse effects of the clinical findings, laboratory examination and the pathology observed in the 120 mg/kg/day treatment group, the NOAEL of yonkenafil hydrochloride was considered to be 7 mg/kg/day under the present experimental conditions in beagle dogs.
Acknowledgements
We are grateful for the generous gift of yonkenafil hydrochloride provided by Tianjin Tasly Company Ltd. (Tianjin, P.R. China). The authors also wish to thank Professor Xueyong Li and Ms Hui Li, Jin Li for their technical aid on experimental animals and Ms Yan Liu and Mr Chenghe Li for technical assistance on histopathology.
Conflict of Interest
The authors declare that there are no conflicts of interest.
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