Application of composition containing riluzole and borneol in preparation of medicine for treating cerebrovascular diseases
A composition and technology for cerebrovascular diseases, applied in the direction of medical preparations containing active ingredients, drug combinations, cardiovascular system diseases, etc., to achieve the effect of increasing drug efficacy
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Embodiment 1
[0028] Example 1 Effects of riluzole and d-camphenol NMDA-induced excitatory damage in primary cortical neurons
[0029] 1 Materials and methods
[0030] 1.1 Animals
[0031] SD pregnant rats, Shanghai Slack Laboratory Animal Co., Ltd. (production license number: SCXK (Shanghai) 2017-0005)
[0032] 1.2 Reagents and Consumables
[0033] name Article / Lot Number manufacturer Neurobasal 21103-049 Gibco B27 17504-044 Gibco GlutaMax 2110349 Gibco CellTiter-Glo G7571 Promega Polylysine (PDL) P6407 Sigma DMEM 11995-040 Gibco Sugar-free DMEM 1763966 Gibco Pennicillin Streptomycin (P / S) 15140-122 Gibco Fetal Bovine Serum (FBS) 10099-141 Gibco Cell Culture Plate Corning 3610 / 96 well cell culture plate Corning Riluzole R129533-5g (Lot1502089) Aladdin Dex-camphenol KC20171205-1-2 Jiangsu Ouwei Pharmaceutical Co., Ltd. Luminescent Cell Viability Assay LOT 7E322D9 Nanjing...
Embodiment 2
[0050] Example 2 The effect of riluzole and d-camphenol composition on NMDA-induced excitatory injury of primary cortical neurons
[0051] 1 Materials and methods
[0052] 1.1 Animals Same as Example 1
[0053] 1.2 Reagents and consumables are the same as in Example 1
[0054] 1.3 Preparation of primary cortical neurons Same as Example 1
[0055] 1.4 NMDA-induced excitatory injury test of primary cortical neurons
[0056] In vitro matured primary neuronal medium was replaced with Locke's buffer containing varying concentrations of riluzole (R), d-camphenol (B), or a combination of riluzole and d-camphenol (RB) (see Table 1). solution (NaCl 154mM, KCl 5.6mM, NaHCO 3 3.6mM, CaCl 2 2.3 mM, D-Glucose 5.6 mM, HEPES 5 mM, pH 7.4), after incubation at 37°C for 10 min, add excitability inducers (NMDA final concentration 100 µM and Glycine final concentration 10 µM) for 30 min; aspirate and discard the induction buffer containing 1 mM MgCl 2 After washing once with Locke’s buff...
Embodiment 3
[0066] Example 3 Synergistic study of riluzole and d-camphenol composition (20:1) in protecting primary neurons from excitatory injury
[0067] 1 Materials and methods
[0068] 1.1 Animals Same as Example 1
[0069] 1.2 Reagents and consumables are the same as in Example 1
[0070] 1.3 Preparation of primary cortical neurons Same as Example 1
[0071] 1.4 NMDA-induced excitatory injury test of primary cortical neurons
[0072] In vitro matured primary neuron culture medium was replaced with Locke's buffer ( See Table 2), after incubation at 37 °C for 10 min, add excitability inducers (final concentration of NMDA 100 µM and Glycine final concentration 10 µM) for 30 min; after aspirating and discarding the induction buffer, add 1 mM MgCl 2 After washing once with Locke’s buffer, change to completion medium (100 μL / well) to resume culturing for 4 h.
[0073] Table 2 The concentration design of riluzole dex-camphenol composition
[0074] Riluzole (µM) Dex Camphen...
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Abstract
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