Medicine composition for treating neurosis
A technology of composition and medicine, which is applied in the field of pharmaceutical composition for the treatment of neurosis, can solve the problems of narrow application range and single effect in clinical application, and achieve the effects of less adverse reactions, good therapeutic effect and low recurrence rate
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Embodiment 1
[0038] Example 1: Experiment of the drug of the present invention against the eyelid drooping caused by reserpine in mice
[0039] experimental method
[0040] The Pharmacology Department of Basic Medical College of Hebei Medical University used 40 Kunming mice, half male and half male, and randomly divided into a blank control group, a positive drug control group, an experimental group 1 and an experimental group 2, a total of 4 groups. Each of the above groups was given liquid with a volume of 0.2ml / 10g body weight by gavage, the blank control group was fed only water; the positive drug control group was intraperitoneally injected with imipramine 25mg / kg, and the experimental group was given the powder of the present invention at 1.0g / kg, Gavage 2.0g / kg (divided into experimental group 1 and experimental group 2) for 7 days; 1 hour before the last dose, observe whether there is ptosis, and then immediately inject reserpine 0.5 mg / kg subcutaneously , 5 hours later, the degree of ...
Embodiment 2
[0048] Example 2: The effect of the drug of the present invention on prolonging the sleep time of mice induced by pentobarbital sodium
[0049] experimental method
[0050] Fifty Kunming mice, half male and half male, were randomly divided into 5 groups: blank control group, positive control group, and experimental group. Each of the above groups was given liquid with a volume of 0.2ml / 10g body weight by gavage, the blank control group was fed only water, the positive control group was given intraperitoneal injection of imipramine 25mg / kg, and the experimental group was given the powder of the present invention at 0.5g / kg, 1.0g / kg, 2.0g / kg gavage (divided into three groups of experimental group 1, experimental group 2, and experimental group 3) for 3 days; 30 minutes after the last administration, sodium pentobarbital 50mg / kg Intraperitoneal injection, taking the disappearance of the righting reaction as a sleep indicator, observe the effect of each group on prolonging the sleep t...
Embodiment 3
[0055] Example 3: Acute toxicity experiment of the drug of the present invention.
[0056] experimental method
[0057] Take 20 Kunming mice, weighing 18-22g, half male and half, take 30g of the medicine powder of the present invention, add water to 75mL, grind to prepare a 40% suspension, give 0.4ml / 10g body weight and give a total of 3 Times, the administration interval is 2 hours. After the first administration, the mice foraging, drinking, and activities were normal; after the second administration, the mice squatted with their eyes closed and their response to stimuli decreased. 1.5 hours after the administration, loose stools appeared on 9 / 20. After the third administration, the mice appeared lethargic and all had loose stools about 1 hour after the administration. The activities and behaviors of all mice returned to normal on the second day after administration. A total of 7 days of observation, no death occurred. The male mice weighed 21.4±1.1g before the experiment and 24...
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