Use of a GABA.SUB.A .receptor allosteric enhancer in medicine

Abstract

An application of a GABA.sub.A receptor allosteric enhancer in medicine. Specifically provided is use of the GABA.sub.A receptor allosteric enhancer shown in formula (I) in preparation of drugs for sedatives, hypnosis, treatment or prevention of anxiety, depression, insomnia, nausea, vomiting, migraine, schizophrenia, convulsions, and ##STR00001##

Claims

1. A method of treating epilepsy, comprising administering a GABA.sub.A receptor allosteric enhancer represented by formula (I): ##STR00004##

2. The method according to claim 1, wherein the epilepsy is an epilepsy that causes neuron loss in the hippocampus.

3. The method according to claim 1, wherein the epilepsy is temporal lobe epilepsy.

Description

BRIEF DESCRIPTION OF DRAWINGS

(1) FIG. 1 is a diagram of the changes in Compound 1 and dipropofol concentrations in brain tissues at different points in time after administration in rats.

(2) FIG. 2 provides the number of spontaneous seizure episodes in the KA-induced chronic epilepsy model in Experimental Example 1.

(3) FIG. 3 is the neuronal cell survival rate of the KA-induced chronic epilepsy model in Experimental Example 1.

DESCRIPTION OF EMBODIMENTS

(4) The technical solutions of the present disclosure will be described in details below in conjunction with the accompanying drawings and examples and are encompassed by, but not limiting the protection scope of this disclosure.

Example 1

Preparation of 4,4′-dihydroxy-3,3′-diisopropyl-5,5′-dipropylbiphenyl (Compound 1)

(5) ##STR00003##

(6) (1) In a 25 mL round bottom flask, o-isopropyl phenol (1.0 g, 7.3 mmol) and allyl bromide (14.6 mmol) were consecutively added and dissolved with dichloromethane;

(7) (2) In another 50 mL flask, benzyl tributyl ammonium bromide (0.26 g, 0.73 mmol) was added and dissolved with a 1M NaOH solution;

(8) (3) At room temperature, the solution obtained in (1) was slowly added into the solution obtained in (2), and stirred at room temperature for 2 h; the organic phase was separated, and the water phase was extracted with dichloromethane; the organic phase was combined, washed with water and saturated sodium chloride, dried over anhydrous sodium sulfate, and concentrated to obtain a colorless liquid; under the protection by nitrogen, the liquid was heated at 250° C. for 2 h, and then cooled and subjected to column chromatography to obtain a colorless liquid; the colorless liquid was dissolved in anhydrous ethanol, into which Pd/C was added for reduction; after the reduction, suction filtration was carried out, and the resultant mother was concentrated to give 2-isopropyl-6-propylphenol;

(9) .sup.1H NMR (400 MHz, CDCl.sub.3) δ 7.06 (dd, J=7.6, 1.6 Hz, 1H), 6.97 (dd, J=7.5, 1.6 Hz, 1H), 6.85 (t, J=7.6 Hz, 1H), 4.75 (s, 1H), 3.22-3.13 (m, 1H), 2.59-2.54 (m, 2H), 1.72-1.59 (m, 2H), 1.26 (d, J=6.9 Hz, 6H), 0.99 (t, J=7.3 Hz, 3H);

(10) (4) 2-isopropyl-6-propylphenol (1.0 g, 5.6 mmol) was dissolved in 20 mL dichloromethane, into which a catalyst, Cu(OH)Cl.TMEDA (N,N,N,N-tetramethylethylenediamine basic copper chloride) (50 mg, 0.1 mmol), was added and stirred at room temperature to obtain a red solid quinone; then, it was reduced with sodium dithionite to give 4,4′-dihydroxy-3,3′-diisopropyl-5,5′-dipropylbiphenyl (1.1 g, 55.5%).

(11) 4,4′-dihydroxy-3,3′-diisopropyl-5,5′-dipropylbiphenyl: .sup.1H NMR (300 MHz, CdCl.sub.3) δ 7.29 (s, 4H), 6.52 (s, 2H), 3.13-3.08 (m, 2H), 2.43-2.40 (m, 4H), 1.51-1.43 (m, 4H), 1.03 (d, 12H), 0.84-0.81 (m, 6H).

Experimental Example 1

(12) 1. Comparative Test of the Distribution in Brain Tissues of Compound 1 and Dipropofol (3,3′, 5,5′-Tetraisopropyl-4,4′-Biphenol) after Intravenous Administration in Rats

(13) 72 SD rats, weighing 200 to 220 g, were randomly divided into 12 groups (6 per time group), and fasted for 12 h before administration. A dose of 45 mg/kg was intravenously administered with Compound 1 or the dipropofol respectively, and the rates were sacrificed at 5 min, 15 min, 30 min, 1 h, 2 h and 4 h after the administration. The brain tissues were removed immediately, rinsed with ice-cold distilled water, blotted dry, and frozen at −40° C. for storage. The concentration of Compound 1 or the dipropofol in the brain tissues at different points in time after administration in rats was measured by LC-MS/MS, as shown in Table 1 and FIG. 1.

(14) TABLE-US-00001 TABLE 1 Drug concentration in brain tissues (ug/g) 5 min 15 min 30 min 1 h 2 h 4 h Com- Male 35.19 42.66 39.78 32.02 22.67 7.75 pound average 1 Standard 3.26 1.89 3.33 2.49 1.60 0.66 deviation Dipro- Overall 12.8 24.1 32.5 26.6 17.9 5.52 pofol average Standard 1.19 1.61 1.99 1.24 0.61 0.51 deviation

(15) The concentration of Compound 1 in the brain tissues at 5 min after intravenous administration was 2.75 times of that of the dipropofol, with the concentration of Compound 1 peaked at 15 min in the brains tissues and the concentration of the dipropofol peaked at 30 min after administration. The AUC.sub.0-4h of Compound 1 in the brain tissues was about 1.31 times of that of the dipropofol.

(16) The above results show that after being intravenously administrated with the same dose, Compound 1 has a significantly higher brain entry rate and brain intake amount than the dipropofol.

(17) 2. In Vitro GABA.sub.A Receptor Target Affinity Test

(18) A radioligand ([.sup.35S] TBPS) receptor competitive binding test was used to evaluate the affinity of the test compound (10 uM) with GABA.sub.A receptors. The results are shown in Table 2 below.

(19) TABLE-US-00002 TABLE 2 Test concen- tration Targets Species (uM) IC50 Dipropofol GABA.sub.A, rats 30, 10, 3, 1, 0.3 2.06 uM Chloride Channel, TBPS Compound 1 GABA.sub.A, rats 30, 10, 3, 1, 0.3 2.93 uM Chloride Channel, TBPS

(20) The results demonstrate that Compound 1 has high affinity for the GABA.sub.A receptors, which affinity is comparable to that of the dipropofol.

(21) 3. Antiepileptic Test of Compounds 1 and Dipropofol (3,3′, 5,5′-Tetraisopropyl-4,4′-Biphenol) in Rats with PTZ-Induced Seizures

(22) In this test, male SD rats (Xi'an Jiaotong University), weighing 200 to 250 g, were used and intravenously administrated with 45 mg/kg of a Dipropofol injection, a Compound 1 injection, and blank solvent of the same volume. 1, 3, 5, 10, 15, 30, 60, 90 mins, and 120 mins after the intravenous administration, 70 mg/kg of PTZ was intraperitoneally injected in the rats to induce tonic-clonic seizures. 7 rats were used for each time point in each drug group. Rat seizure intensity was recorded in accordance with the Racine grading criteria in grade III to V seizure status. Scores were recorded according to the seizure intensity: 5 points for grade V, 4 points for grade IV, 3 points for grade III, and 0 point for below grade III. The seizure intensity for each group of animals was the total score of 7 animals, and the results are shown in Table 3 below.

(23) TABLE-US-00003 TABLE 3 Scores of seizure grade and intensity of animals at various time points after administration for prevention purpose Model Dipropofol Compound 1 Number of Number of Number of n = 7 episodes episodes episodes Time (animals) Seizure (animals) Seizure (animals) Seizure point III IV V Intensity III IV V Intensity III IV V Intensity   1 min 0 0 7 35 0 7 0 28 2 2 0 14   3 min 0 0 7 35 2 5 0 26 0 0 0 0   5 min 0 0 7 35 3 3 0 21 0 0 0 0  10 min 0 0 7 35 2 2 0 14 0 0 0 0  15 min 0 0 7 35 0 0 0 0 0 0 0 0  30 min 0 0 7 35 0 0 0 0 0 0 0 0  60 min 0 0 7 35 0 0 0 0 0 0 0 0  90 min 0 0 7 35 0 0 0 0 0 0 0 0 120 min 0 0 7 35 2 1 0 10 0 0 0 0

(24) The experimental results show that 3 to 5 minutes after being intravenously injected, Compound 1 can completely inhibit PTZ-induced major seisures, and the potency can be maintained for 120 minutes or more after administration. However, it was not until 15 minutes after intravenous injection of the bisphenol that the PTZ-induced major seizures are completed inhibited, and the potency begins to decline at 90 minutes after administration. As seen from the above results, the compound of this disclosure acts at a significantly faster rate than the dipropofol, with the peak potency maintained for a duration longer than the latter.

(25) 4. KA-Induced Chronic Epilepsy Model

(26) A chronic epilepsy animal model was established by microinjection of kainic acid (KA) in the hippocampus: 0.2 ug (2 ul) KA was injected into the hippocampus of mice by using a stereotaxic device. Within 6 hours after modeling, the mice had seizures. Within 3 weeks after modeling, the mice developed spontaneous seizures. Mice with spontaneous seizures after modeling were divided into two groups (n=10): Compound 1 administration group and saline administration group. On day 2 after modeling, Compound 1 (100 mg/kg) and saline of the same volume was intravenously administered, respectively. 3 weeks after modeling, the number of episodes of spontaneous seizures in the mice was observed for 2 weeks (FIG. 2). After the observation, the mice were sacrificed, hippocampal tissue sections were taken, and NeuN staining was used to calculate the survival rate of neurons in the CA1 area (FIG. 3).

(27) The results show that the administration of the compound of the present disclosure in KA-induced chronic epilepsy model animals can not only significantly inhibit spontaneous seizures, but also significantly inhibit hippocampal neuron death induced by the epilepsy model.