Application of leonurine to preparation of medicine for treating vascular dementia
A technology of vascular dementia and motherwort, which is applied in drug combination, nervous system diseases, etc.
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Embodiment 1
[0035] Example 1. Leonurine improves the spatial learning and memory ability of rats
[0036]After the experimental rats were successfully anesthetized with 10% chloral hydrate, they were fixed on the operating table in a supine position, and after routine disinfection, an incision was made in the middle of the rat’s neck, and the muscles were bluntly separated to expose the bilateral common carotid arteries and threaded with a No. 0 silk thread. After ligation, the muscles were reset and the skin was sutured. After the rats woke up, they were put back into the cage for routine feeding. The operation of the sham operation group was the same as that of the model, but only the bilateral common carotid arteries were separated without ligation. Rats in the postoperative model + motherwort group were given 60 mg / kg / day of motherurine by intragastric administration for 3 weeks. After the administration, the Morris water maze test (MWM) was carried out to test the spatial learning a...
Embodiment 2
[0037] Example 2. Effect of Leonurine on Percentage of Residence Time in Each Quadrant in the Reverse Learning Training Process of Rats
[0038] The specific implementation method is the same as in Example 1. Record the percentage of swimming time in each quadrant of the rats in the reverse learning phase (day 6 to day 7) (see Figure 7 ,8,9,10), and recorded the data of rat swimming trajectory (see Figure 11 ).
[0039] The result is as figure 2 As shown, compared with the sham operation group, the time of swimming exploration in the original target quadrant (zone 1) of the rats in the model group was significantly prolonged on the 7th day (see Figure 7 ) (P Figure 7 ), increasing its swimming time in the new target quadrant (zone 4) (see Figure 10 ) (P<0.05).
Embodiment 3
[0040] Example 3. Effect of Leonurine on LTD in Rat Hippocampus CA3-CA1 Region
[0041] Rats were anesthetized with 30% urethane intraperitoneally (4ml / kg), fixed on a stereotaxic instrument, exposed the skull, and positioned CA3 (4.2 mm behind the bregma, 3.5 mm beside the midline, and 2.5 mm below the dura mater) and CA1 area (3.5mm posterior to bregma, 2.5mm lateral to midline, 2.0mm subdural). After obtaining a stable representative waveform, the baseline was recorded for 20 min, and then a low-frequency stimulation of 900 pulses at 1 Hz was given for a total of 15 min to induce long-term post-synaptic depression. Then restore the single-stimulus method during base recording, and record for 60 minutes. The result is as image 3 As shown, compared with the sham operation group, the slope of the fEPSPs of the model group rats was significantly improved (see Figure 12 and Figure 13 ) (P Figure 12 and Figure 13 ) (P<0.05).
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