Application of male hippocampus japonicus to preparation of medicine or preparation for improving desperation and helplessness behaviors of depression
A depression and drug technology, applied in the field of medicine, can solve problems such as unclear molecular mechanism, achieve the effect of improving depression and desperate behavior, and restoring the level of neurotransmitters in the brain
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Embodiment 1
[0033] Example 1 Effect of Male Hippocampus on Forced Swimming Test in Mice
[0034] 1. Establishment of mouse depression model
[0035] Refer to Papp and Willner (Papp et al. , 1992) and modified for applicability, the animals were repurchased and adapted to the laboratory for one week, and randomly numbered and divided into groups, a total of 4 groups were set up, as shown in Table 1:
[0036] Table 1 Grouping of experimental animals
[0037]
[0038] The CUMS group and the CUMS+Seahorses group were exposed to the following stressors as model treatments; the Control group and Seahorses groups were reared under standard conditions without stress treatment.
[0039] All the stressors were randomly operated independently, and it was guaranteed not to be repeated within a week to prevent the animals from adapting. Two stressors were operated independently every day, and after 8 weeks of continuous stress, the behavior was measured. Stress sources include: water deprivatio...
Embodiment 2
[0044] Example 2 Effect of Male Hippocampus on the Contents of Neurotransmitters and Metabolites in Mouse Hippocampus
[0045] 1. Extraction of fatty acids from mouse hippocampal brain tissue
[0046] After the mice were decapitated and sacrificed, the hippocampal tissues were quickly isolated on ice, frozen in liquid nitrogen, and then transferred to -80°C for storage.
[0047]Total fatty acid extraction: tissue homogenate, operate in a fume hood, add 10.5mL chloroform / methanol (the volume ratio of the two is 2:1) solution to each tube, 100μL content is 2mg / mL C23:0 as internal standard, fill into N 2 Close the lid tightly, vortex for 30s, and then ultrasonically clean for 10-15min until there is no obvious block; vortex again for 30s, then add 2.6mL 0.88% NaCl solution, fill with N 2 Then close the lid tightly, vortex again for 15s; centrifuge at 500r / min for 20min.
[0048] Preparation of filter unit: with CH 2 CL 2 Drop washing glass funnel (about 6-10cm in diameter),...
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