Use of Poria cocos extract and turmoacin for muscle protection
A Poria cocos extract and extract technology, applied in the field of muscle protection of Poria cocos extract and turmoic acid, can solve problems such as no effective treatment or delay of muscle atrophy
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Embodiment 1
[0042] Example 1: Preparation and component analysis of Poria cocos extract
[0043] (1-1)
[0044] Take the medicinal material of Poria cocos (the place of origin is Yunnan), wash and peel off its outer skin (hereinafter referred to as "Poria cocos skin part"), and the rest is the meat part (hereinafter referred to as "Poria cocos meat part").
[0045] (1-2)
[0046] Get 700 kilograms of Poria cocos meat part of (1-1), soak in 75% ethanol with the volume ratio of about 1:8 (Poria cocos meat part: 75% ethanol) at room temperature, last 12 hours, then boil and carry out extraction (duration 3 hours). The aforementioned extraction steps were repeated for a total of three times. The extracts from the three extractions were combined and filtered to remove insolubles. Then, concentrate under reduced pressure to remove ethanol, and then dry with a spray dryer to obtain an extract.
[0047] (1-3)
[0048]With liquid chromatography / ultraviolet light / mass spectrometry (LC / UV / MS, ...
Embodiment 2
[0059] Example 2: Establishment of muscle cell injury model
[0060] Tumor necrosis factor alpha (TNF-α) is a pro-inflammatory cytokine (cytokine) with a molecular weight of 17,000. Human clinical data show that in some special diseases (such as cancer, AIDS, chronic obstructive pulmonary disease, etc.) muscle breakdown) or increased muscle cell death. Studies have shown that injecting TNF-α into experimental animals or administering drugs to increase the concentration of TNF-α in experimental animals will induce muscle cell damage (including muscle protein metabolism imbalance, muscle cell death, etc.), and then lead to muscle atrophy. In order to investigate the efficacy and mechanism of Poria cocos extract and its components in protecting muscle, the inventor induced TNF-α to establish a muscle cell injury model.
[0061] First, C2C12 cells (i.e., mouse myoblasts, purchased from ATCC) were cultured with H-DMEM medium (purchased from Sigma Company), until the C2C12 cells g...
Embodiment 3
[0063] Example 3: Effect of Poria cocos extract on anti-muscle cell damage
[0064] The Poria cocos extract provided in Example 1 (1-4) was used to prepare a Poria cocos meat extract solution with dimethyl sulfoxide (DMSO; purchased from Sigma). After the C2C12 cells grew to 80% confluence in H-DMEM medium, they were divided into five groups and processed as follows:
[0065] (1) Control group: cultured in H-DMEM medium (without Poria cocos extract) for 6 hours. Next, the culture medium was replaced with a differentiation medium of 2% horse serum for 4 days.
[0066] (2) TNF-α group: cultured in H-DMEM medium for 6 hours. Next, the medium was replaced with 2% horse serum differentiation medium, and TNF-α was added to the medium at a final concentration of 10 ng / ml for co-treatment with the differentiation medium for 4 days.
[0067] (3) TNF-α + Poria cocos extract group (three groups in total): add the above-mentioned Poria cocos meat extract solution to the H-DMEM medium, ...
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