Kang injection on brain ischemic brain injury.docVIP

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Kang injection on brain ischemic brain injury

 PAGE \* MERGEFORMAT 9 Kang injection on brain ischemic brain injury [Abstract] Objective To observe the brain Kang injection on ischemic brain injury. Methods according to different doses of continuous intravenous and oral administration, separation of both sides of the common carotid artery, a double ligation, seizures and cerebral ischemia and measured the time of death , measured by electromagnetic flowmeter. Results Naokangling injection and high dose group spontaneously hypertensive rats stroke (SHRSP cerebral ischemic injury prevention, and can significantly reduce the acute incomplete cerebral ischemia in rats MDA, increased SOD activity. Conclusion Naokangling injection can significantly improve the SHRSP cerebral ischemia and acute experimental cerebral ischemia, delayed the death of SHRSP rats and improve the level of free radicals. [Keywords:] brain health injection, rat, cerebral ischemia, injury, the role of Drugs at home and abroad for the treatment of stroke has not been a breakthrough, which in Chinese medicine for effective treatment of stroke drugs has important clinical significance. Naokangling injection mainly yam and ginseng saponins saponin composition, with Yi Qi Tong Luo, stasis of the effect, intended for clinical treatment of ischemic stroke and stroke sequelae (1). To ensure the effectiveness of clinical treatment, reliability, the author carried out its Pharmacodynamic study. 1 Materials and methods 1.1 Materials 1.1.1 Experimental animal stroke spontaneously hypertensive rats (SHRSP was purchased from Chinese Academy of Medical Sciences, Institute of Laboratory Animal line with a standard of either sex, 210 ~ 250 g, 3 months old, moving Xu Jing Certificate of Conformity for the 017 words . Healthy Wistar rats were purchased from Animal Center of PLA University of Agriculture and Animal Husbandry, either sex, 180 ~ 300 g, 18 ~ 22 g, Certificate of Conformity for the 105 112 animals. 1.1.2 Experimental drugs and

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