2.1 Chemical experimental part
The chemical reagents used in the synthesis were obtained from commercial suppliers and used without purification. All solvents were dried and purified by standard procedures if required. Melting points were measured in open capillary tubes using OptiMelt melting point apparatus (Stanford Research Systems, USA). The structures of the compounds were confirmed by elemental analysis and 1H NMR spectroscopy. The NMR spectra were obtained on a Bruker Fourier 300 (Bruker, Germany) spectrometer using tetramethylsilane as an internal standard. The NMR peaks were designated as follows: s, singlet; d, doublet; t, triplet; and m, multiplet. Microanalyses for C, H, and N agreed with calculated values within 0.4%. Specific optical rotations were recorded by automatic polarimeter ADP 440 (Bellingham + Stanley Ltd., England). The TLC was carried out on Merck silica gel 60 F 254 plates with spot visualization by iodine vapor or UV light.
N-Phenylacetyl-glycine.13.24 ml (0.1 mol) of N-phenylacetyl chloride and 25 ml of 4 M NaOH were added dropwise successively to a solution of 7.5 g (0.1 mol) of glycine in 25 ml of 4 M NaOH under stirring at −10°С. The reaction mixture was stirred for 30 min on cooling, extracted by ethyl acetate (3 × 15 ml) to remove impurities and unreacted N-phenylacetyl chloride. Then the solution was acidified by 4 М HCl to pH 2–3; the resulting precipitate was filtered, washed with cooled distilled water, and dried in air. The yield of N-phenylacetyl-glycine was 5.83 g (30%); m.p. 143–144°С; Rf0.8 (BuOH/AcOH/H2O, 4:1:1). 1H-NMR spectrum (DMSO-d6 + CF3COOD, d, ppm): 3.47 (s, 2Н, СН2Ar), 3.76 (d, J6.0 Hz, 2Н, СН2 Gly), 7.27 (m, 5H, ArH), 8.40 (t, J6.0 Hz, 1Н, NH Gly). Lit. data [17]: m.p. 138–143°С.
H-L-Pro-OC2H5·HCl.2.54 ml (35 mmol) of thionyl chloride was added dropwise to 60 ml of anhydrous ethanol cooled to −20°С. Then 2.0 g (17.5 mmol) of L-proline was added portionwise under vigorous stirring. The resulting mixture was stirred for 2 h at −5°С and then for 2 h at room temperature. The solvent was removed in vacuo. This operation was repeated twice, each time adding 30 ml of anhydrous ethyl alcohol to afford 2.4 g (77%) of L-proline ethyl ester hydrochloride as an oil. [α]23 D−43° (с3, EtOH); Rf0.75 (i-PrOH/NH3, 7:3). 1H-NMR spectrum (DMSO-d6, d, ppm): 1.19 (m, 3Н, СН3СН2О), 1.8–2.1 (m, 4Н, СγН2 Pro, СβН2 Pro), 3.2 (m, 2Н, СδН2 Pro), 4.2 (m, 2Н, СН3СН2О), 4.5 (m, 1Н, СαН Pro), 9.9 (br. s, 1Н, NH). Lit. data [18]: oil; [α]23 D−44.8° (с3.03, EtOH).
H-D-Pro-OC2H5·HCl.Obtained similarly to H-L-Pro-OC2H5·HCl from D-proline. [α]23 D + 42.0° (с3, EtOH); Rf0.75 (i-PrOH/NH3, 7:3). 1H-NMR spectrum (DMSO-d6, d, ppm): 1.18 (m, 3Н, СН3СН2О), 1.8–2.1 (m, 4Н, СγН2 Pro, СβН2 Pro), 3.19 (m, 2Н, СδН2 Pro), 4.2 (m, 2Н, СН3СН2О), 4.5 (m, 1Н, СαН Pro), 9.9 (br. s, 1Н, NH). Lit. data [18]: oil; [α]23 D+44.16° (с3.03, EtOH).
N-Phenylacetyl-glycyl-L-proline ethyl ester.1.1 ml (10.0 mmol) of N-methylmorpholine and 1.35 ml (10.0 mmol) of isobutyl chloroformate were added simultaneously at −10°C to a vigorously stirred solution of 1.93 (10.0 mmol) N-phenylacetyl-glycine in dimethylformamide (10 mL). After 2 min a mixture of 1.79 g (10.0 mmol) of proline ethyl ester hydrochloride and 1.1 ml (10.0 mmol) of N-methylmorpholine in dimethylformamide (20 mL) was added dropwise. The reaction mixture was stirred at −10°C for 30 min and then at room temperature for 1 h. The precipitate was separated by filtration; the solvent was evaporated in vacuo; the residue was dissolved in chloroform (25 ml). The solution was washed with 3% solution of NaHCO3 (3 × 7 ml), water (3 × 7 ml), and 1 N HCl (3 × 7 ml). The organic layer was dried with anhydrous Na2SO4, filtered, and evaporated to dryness. The yield of chromatographically homogeneous product was 2.87 g (90%), an orange oil, finally crystallized from ethyl acetate/hexane system. M.p. 111–112°C; [a]23 D−90.0° (с1, water); Rf = 0.80 (dioxane/H2O, 9:1). 1H-NMR spectrum (DMSO-d6, d, ppm): 1.2 (m, 3Н, СН3СН2О), 1.8–2.1 (m, 4Н, СγН2 Pro, СβН2 Pro), 3.5 (s, 2Н, СН2ArH), 3.6 (m, 2Н, СδН2 Pro), 3.85 and 4.0 (2 dd, J17.6 Hz, J5.6 Hz, 2Н, СαН2 Gly), 4.2 (m, 2Н, СН3СН2О), 4.5 (dd, J4.0 Hz, J8.5 Hz, 1Н, СαН Pro), 6.4 (br. t, J5.6 Hz, 1Н, NH), 7.3 (m, 5Н, ArH). Calcd. for C17H22N2O4, %: C, 64.27; H, 7.05; N, 8.63. Found, %: C, 64.13; H, 6.97; N, 8.80.
C6H5-CH2-C(O)-Gly-D-Pro-OEt (GZK-121).Obtained similarly to the L-enantiomer. Yield 64%. M.p. 112–113°C; [a]23 D +90.0° (с1, water); Rf = 0.80 (dioxane/H2O, 9:1). 1H-NMR spectrum (DMSO-d6, d, ppm): 1.2 (m, 3Н,СН3СН2О), 1.85–2.2 (m, 4Н, СγН2 Pro, СβН2 Pro), 3.5 (s, 2Н,СН2Ar), 3.6 (m, 2Н, СδН2 Pro), 3.86 and 4.0 (2 dd, J17.6 Hz, J5.6 Hz, 2Н, СαН2 Gly), 4.2 (m, 2Н, СН3СН2О), 4.5 (dd, J4.0 Hz, J8.5 Hz, 1Н, СαН Pro), 6.4 (br. t, J5.6 Hz, 1Н, NH), 7.3 (m, 5Н, Ar). Calcd. for C17H22N2O4., %: C, 64.27; H, 7.05; N, 8.63. Found, %: C, 63.91; H, 6.90; N, 8.71.
2.2 Biological experimental
2.2.1 Study of GZK-111 metabolism
Blood plasma preparation. Blood plasma of outbred male rats weighing 250–280 g was used. Animals were decapitated, blood was collected in BD Vacutainer® tubes with EDTA, and plasma was obtained by centrifugation at 3000 rpm for 10 min.
Incubation and extraction.A solution of 3 mg of GZK-111 in 100 μl of saline was added to 900 μl of rat plasma. The mixture was incubated at 37°C in a water bath for 10 h. Then, an equal volume of acetonitrile was added to 100 μl of the incubated mixture, the samples were vigorously shaken for 10 min and centrifuged at 12,000 rpm for 10 min, and the supernatant was collected and then chromatographed.
Reverse-phase high-performance liquid chromatography(RP HPLC).HPLC was performed on a Gilson 41 chromatograph (Gilson, USA) with a Gilson 116 UV detector (Gilson, USA). Detection was carried out at 220 nm. A Nucleosil C18 column (4.6 × 150 mm, 5 μm) was used with a flow rate of 0.5 ml/min. The sample volume was 20 μl. The following eluents were used: (solution A) 3.7 mM sodium 1-hexanesulfonate/water (pH 3.5) and (solution B) 3.7 mM sodium 1-hexanesulfonate/40% acetonitrile. The elution was carried out in a gradient according to the following program: (1) 0% B for 3 min, (2) from 0 to 100% B in 20 min, and (3) 100% B for 6 min. The signal was recorded using the Multichrom 1.5 software (Ampersend, RF). Cyclo-L-prolylglycine and N-phenylacetyl-glycyl-L-proline, synthesized in the Medicinal Chemistry Department of the V.V. Zakusov Research Institute of Pharmacology, were used as standards for HPLC.
Calibration curve.Standard solutions of synthetic cyclo-L-prolylglycine were prepared in acetonitrile at the concentrations of 0, 0.1, 0.2, 0.4, 0.8, 1.6, and 3.2 mg/L. The 20 μl aliquot of the solutions were chromatographed under RP HPLC conditions as described above. The calibration curve was calculated based on the peak areas.
2.2.2 In vitro pharmacological study
Cell culture.The studies were carried out on SH-SY5Y human neuroblastoma cells received from the cell bank of the N.N. Blokhin National Medical Research Center of Oncology of the Ministry of Health of the Russian Federation. Cells were grown at 37°C and 5% CO2 in DMEM (HyClone, USA) with 10% FBS (Gibco, USA) and 2 mM L-glutamine (MP Biomedicals, Germany). After the monolayer formation, the cells were counted and placed into 96-well culture plates (Costar-Corning, USA) at a density of 3.5 thousand per well and into 6-well culture plates (Costar-Corning, USA) at a density of 280 thousand per well; both plates were pre-coated with a 0.1 mg/ml solution of poly-D-lysine (BD Bioscience, UK) for 1 h.
Parkinson’s disease model in culture of SH-SY5Y human neuroblastoma cells.Neurotoxin 6-hydroxidopamine (6-OHDA) used in an experimental model of in vitro dopaminergic neuron degeneration according to [19] was applied to simulate Parkinson’s disease in the culture of SH-SY5Y human neuroblastoma cells. 6-OHDA was added into the cell medium at a final concentration of 100 μM 24 h after cell seeding. Then the cells were incubated for 24 h. The neuroprotective effect was investigated by addition of compounds to the culture medium at final concentrations of 10−8–10−5 M 24 h before 6-OHDA. Cell viability was determined after 24 h using the MTT test.
Neuronal viability assessment in culture using the MTT test.MTT (3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide) is a yellow water-soluble tetrazolium salt that easily penetrates into cells. In living cells, MTT transforms into water-insoluble violet formazan crystals, which are dissolved in organic solvents (isopropanol, dimethylformamide, dimethyl sulfoxide) upon completion of the reaction followed by absorption measurements.
At the end of the experiment, the culture medium was replaced with MTT solution (0.5 mg/ml) and incubated for 30 min at 37°C. Then, a MTT solution was removed from the wells, and DMSO was added to dissolve the formazan. Absorbance was measured at 600 nm using a 96-well plate reader Multiscan (Thermo, USA).
2.2.3 In vivo pharmacological studies
In vivo studies were performed in outbred male rats weighing 200–270 g (nootropic and a anxiolytic activity), in outbred male mice weighing 25–28 g (antihypoxic and antidepressant-like activity), and in C57Bl/6 male mice weighing 25–29 g (analgesic activity), received from the Stolbovaya Branch of the Scientific Center of Biomedical Technologies of the Federal Medical Biological Agency (FMBA) of Russia, and in Wistar male rats weighing 200–250 g (neuroprotective activity) received from the Andreevka Branch of the Scientific Center of Biomedical Technologies of the FMBA of Russia. The animals were kept in vivarium under natural circadian light/dark cycles with free access to standard granular feed and water. The study complied with the requirements of Order of the Ministry of Health of the Russian Federation No. 199 “On Approval of the Rules of Good Laboratory Practice” and Decision of the Council of the Eurasian Economic Commission No. 81 “On Approval of the Rules of Good Laboratory Practice of the Eurasian Economic Union in the Area of Circulation of Medicines.” All manipulations with animals were approved by the Bioethical Commission of the Zakusov Research Institute of Pharmacology. The experiments were carried out from 10 to 16 pm. The test substances were dissolved in saline or in distilled water and administered, i.p. The animals of the control groups were injected with saline or with distilled water, respectively.
2.2.4 Neuroprotective activity
A model of focal cerebral ischemia (ischemic stroke).Focal cerebral ischemia was induced by transient middle cerebral artery occlusion (MCAO) using a modification of the intraluminal filament model originally described in [20]. All surgical procedures were performed using titanium microsurgical instruments.
The rats were anesthetized with an i.p. injection of chloral hydrate (350 mg/kg) as a 5% solution in saline. The right common carotid artery, internal carotid artery, and external carotid artery were surgically exposed. A nylon suture (0.25 mm in diameter) with a silicon-coated tip was inserted from the external carotid artery into the internal carotid artery and then to the circle of Willis to occlude the origin of the middle cerebral artery. After 1 h of MCAO, the suture was carefully removed to induce reperfusion. Sham-operated rats (n = 6) underwent identical surgery except that the suture was not inserted. During the surgery the body temperature was maintained at 37.0 ± 0.5°C using a heating pad. Three rats received MCAO without any neurological deficits observed after awakening was excluded.
Design of the study.The rats with experimental ischemic stroke were randomly divided into two groups: a “stroke” group with water treatment (n = 10) and “stroke + GZK-111” group treated with GZK-111 (n = 7). Solution of GZK-111 in distilled water was administered, i.p., at a dose 0.5 mg/kg 6 h after surgery and then once a day for 6 days. Neurological functions were evaluated 3 and 6 days after surgery using the limb-placing test [21]. The infarct volume was evaluated according to [22] using 2,3,5-triphenyltetrazolium chloride (TTC) staining and computerized image analysis 7 days after surgery.
Limb-placing test.Neurological functions were evaluated using the limb-placing test [21], a modified version of the test described by De Ryck et al. [23]. This test assessed the forelimb and hind limb responses to tactile and proprioceptive stimulation and consisted of seven limb-placing tasks. The following scores were used to detect impairment of the forelimb and hind limb: 2 points, the rat performed normally; 1 point, the rat performed with a delay of more than 2 s and/or incompletely; and 0 point, the rat did not perform the task. The maximum possible score for the sham-operated rats for each side of the body was 14. Rats with experimental stroke exhibited decreased neurological score on the side of the body which is opposite to the ischemic lesion.
Evaluation of cerebral infarct volume.The cerebral infract volumes measured with TTC staining were used to describe the severity of cerebral ischemia. The animals were deeply anesthetized with chloral hydrate (350 mg/kg, i.p.) and then decapitated. The brains were removed rapidly, frozen in −20°C for 10 min and then sectioned coronally into 2-mm-thick slices. The brain slices were incubated with 2% TTC at 37°C for 30 min. Stained slices were fixed in 10% formalin solution. The slices were digitalized on a flatbed scanner at 2400 dpi. The infarct volumes were measured using the ImageJ (National Institutes of Health, Bethesda, MD, USA) image analysis software program. The total infarct volume for each brain was calculated by summation of unstained areas of the subsequent slices and multiplying by the thickness (2 mm).
Nootropic antiamnesic activity.The antiamnesic effect of the substances was evaluated by their ability to prevent impaired reproduction of the conditioned passive avoidance reflex (passive avoidance reaction) caused by electroconvulsive shock (ECS). Compounds GZK-111 and GZK-121 were administered once, i.p., at the doses of 0.1, 0.5, and 1.0 mg/kg 40 min before training. Control animals were injected with the same volume of physiological saline.
Passive avoidance reaction was developed in rats in a certified Lafayette Instrument Co installation (USA) according to the method of [24] using a single training procedure. The illuminated start platform (25 × 7 cm) was connected to a dark 40 × 40 × 40 cm chamber equipped with an electrified floor through a square guillotine door. The animal was placed on the start platform with its tail to a dark chamber. When governed by the hole exploratory behavior, the rat found the entrance and passed into the dark compartment; the hole was closed. In the dark chamber, eight unavoidable electric pain stimuli were applied through the floor to the rat (the training current was 0.45 mA, the duration of each pulse was 1 s, and the interval between consecutive pulses was 2 s). Immediately after this, the rat was removed from the dark chamber and subjected to EKS (250 V, 120–122 mA, 0.1 s) applied transcorneally using a certified Harvard apparatus (Germany). After 24 h, the animal was again placed on the illuminated platform for learning test. The latent period of the first animal entry into the dark chamber was recorded. Antiamnesic activity (AA) was calculated as Eq. (1):
AA%=LPtest−LPamnLPcontrol−LPamn×100%E1
where AA% is antiamnesic activity, LPtest is the average latent period of entry into the chamber in the animals administered with the test compound and subjected to amnesia, LPamn is the average period of entry into the chamber in the animals administered with 0.9% NaCl and subjected to amnesia, and LPcontrol is the average latent period of entry into the chamber in animals administered with 0.9% NaCl without amnesia.
Antihypoxic activitywas studied in a model of normobaric hypoxia with hypercapnia (“canned” hypoxia), according to [25]. Tests were performed on animals of the same weight (scatter in groups of ≤2 g). Each group consisted of 10 animals. The substances were administered, i.p., in saline 1 h before the start of the experiment. Antihypoxic activity of the compounds was studied at doses of 0.1, 0.5, and 1.0 mg/kg. Control animals received an equivalent volume of saline. Animals were placed singly into 200 cm3 containers that were hermetically sealed. Deaths of animals were recorded as the final agonal gasp.
Anxiolytic activitywas studied in an elevated plus maze test according to Pellow [26]. Compounds were administered once, i.p., 15 min before the experiment. GZK-111 was administered at doses of 0.75, 1.5, and 3.0 mg/kg and GZK-121 at a dose of 1.5 mg/kg. The control animals were administered with the saline. The apparatus consisted of four arms elevated 60 cm above the floor, with each arm positioned at 90° relative to the adjacent arms. Two opposite arms were enclosed with high opaque walls (50 × 15 × 30 cm), and the other arms were open (50 × 15 × 1 cm) connected via a central area (14 × 14 cm) to form a plus sign. At the beginning of the experiment, the rats were placed in the center of the maze, randomly orientated relative to the arm entrance. The behavior of the animals was evaluated within 5 min. The following indicators were recorded: the number of visits to all arms, the number of visits to open arms, the time spent in all arms, and the time spent in open arms. The anxiolytic effect of the compound was estimated by the increase in the number of visits to the light arms and in the time spent in the light arms and on the central platform.
Antidepressant-like activitywas assessed in a forced swimming test [27]. Mice were placed into cylinders (30 cm high and 10 cm in diameter), filled in two-thirds with water at a temperature of 22°C for 5 min; the time of preservation of the characteristic immobilization posture (rejection of active defensive and research behavior) was estimated. The behavior of animals was recorded using a video camera. Video recording of the experiment was processed in semiautomatic mode using the RealTimer program (Open Joint-Stock Company Open Science LLC). A decrease in the immobilization duration was regarded as a manifestation of antidepressant activity.
Analgesic activity.The hot plate test was used to evaluate the nociceptive response. Latent reaction period (the time before the hind paw pulling and/or jumping) was recorded with a Ugo Basile analgesimeter (Italy). 1–2 hours before the experiment, animals were selected following the basic response in the experimental model conditions and excluding mice that remained on a plate heated to 55 ± 0.5°C for longer than 10 s. A latent period of 20 s (cutoff value) was regarded as 100% analgesia. Hot plate tests were performed before and 30, 60, 90, and 120 min after i.p. drug injection. If no response occurred within 20 s, the mice were removed from the hot plate to avoid tissue injury. The percentage of the maximum possible effect (% MPE) was calculated as follows: postdrug latency−predrug latency×100/cutoff value−predrug latency.
Statistical analysisof the biological results was performed using the standard software package “Statistica 10.0” (StatSoft, Inc., USA). To evaluate statistically significant differences between the experimental and control groups of animals, the following tests were used: nonparametric Mann-Whitney U test for nootropic, anxiolytic, antihypoxic, and neuroprotective effects, the unpaired Student t-test for antidepressant effect, and Duncan criterion for analgesic effect. The means and standard errors of the mean (m ± SEM) were calculated. Kruskal-Wallis ANOVA followed by Dunn’s posttest was used to compare three or more samples in in vitro experiments. The means and standard errors of the mean (m ± SD) were calculated. The results were evaluated as significant at p ≤ 0.05.
