Chinese Herbal Aqueous Extract Having Anti-Anxiety Activities and Method of In Vitro Evaluating the Same
a technology of anti-anxiety activity which is applied in the field of active substances having anti-anxiety activities and in vitro evaluation of the same, can solve the problems of anxiety that cannot be effectively improved, existing anti-anxiety drugs or sleeping drugs, and the nerve system suffers injury under oxidative pressure and hyper-excitatory electrical potential, and achieves the effect of enhancing the expression of the cannabinoid receptor type-1 (cb1) in the membran
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example 1
Establishment of In Vitro Cell Platform
[0046]1. Cell Culture of Human Neuroblastoma Cell Line IMR-32 and Human Glioblastoma U-87 MG
[0047]Human neuroblastoma cell line IMR-32 (deposited at ATCC under accession No.: ATCC CCL-127) and human glioblastoma U-87 MG (deposited at ATCC under accession No.: ATCC HTB-14) were purchased from the Food Industry Research and Development Institute (FIRDI), Bioresource Collection and Research Center (BCRC), Hsinchu, Taiwan). The cell lines IMR-32 and U-87 MG were cultured in the minimum essential medium (MEM; Gibco® BRL, Grand Island, N.Y.) that contained 2 mM L-glutamine, 1 mM non-essential amino acids, 10% fetal bovine serum (FBS), 0.1 mg / mL streptomycin and 0.5 mg / mL ampicillin. Those cells were incubated for 48 hours in an incubator (NUAIR NU4500, USA) with 5% CO2 humidified atmosphere at 37° C., and changed with the fresh medium every two or three days. When those cells reached about 90% confluence, the cells were gently washed in phosphate buf...
example 2
In Vitro Evaluating Chinese Herbal Aqueous Extract
[0055]This EXAMEPLE was directed to evaluate the anti-anxiety activities of the Chinese herbal aqueous extracts of EXAMPLE 1 in vitro by using the epileptic cell platform established by EXAMPLE 1.
[0056]1. Evaluation of Cell Viability
[0057]In this EXAMPLE, cell viability of EXAMPLE 1 was detected by using MTT test. At first, methylthiazoletetrazolium (MTT; Sigma, St. Louis, Mo., USA) solution was prepared by adding 5 mg MTT into 1 mL PBS. Next, each well (i.e. 1×105 cells / well) of 96-well microplate was added with 10 μL MTT solution, incubated for 24 hours in the incubator (NUAIR NU4500, USA) in the dark with 5% CO2 humidified atmosphere at 37° C., and then centrifuged for 10 minutes in a rotation speed of 1,000×g at 4° C. The supernatant was discarded and 100 μL dimethyl sulfoxide (DMSO; Merck, Darmstadt, Germany) solution is added. The microplate was vibrated gently for 10 minutes. Absorbance at 550 nm (OD550 nm) of each well was de...
example 3
In Vivo Evaluating Anti-Anxiety Activities of Chinese Herbal Aqueous Extract by Using Experimental Animal Model
[0070]This EXAMEPLE was directed to evaluate the anti-anxiety activities of the Chinese herbal aqueous extracts of EXAMPLE 1 in vivo by using an animal model.
[0071]1. Establishment of Experimental Animals
[0072]1.1 Care of Experimental Animals
[0073]In this EXAMPLE, fifty six-week-old specific pathogen-free (SPF) imprinting-control-region (ICR) mice (purchased from BioLASCO Taiwan Co., Ltd., Yi-Lan, Taiwan) were randomly allocated into four experimental groups (i.e. PO group, SBO group, AC group and SZS group) and one control (PBS) group, each group of which had ten mice.
[0074]All ICR mice were bred in a SPF environment with positive air pressure. Ambient temperature was controlled at 24° C., relative humidity at 65±5. In addition, the animals were maintained on a reverse 12 h light-dark cycle. Mice were provided with standard laboratory chow and water ad libitum. All experim...
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