Purpose of Lactobacillus reuteri GMNL-263 for preparing hypolipidemic composition
A technology of Lactobacillus reuteri and a composition is applied in the field of use for preparing blood lipid-lowering compositions, and can solve problems such as probiotics for lowering blood lipids that are rarely discussed
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[0023] Preparation of GMNL-263 heat-killing bacteria: Lactobacillus reuteri GMNL-263 is stored in Jingyue Biotechnology Co., Ltd. strain depository. The standard strain Lactobacillus reuteri GMNL-263 stored in a frozen vial was inoculated into MRS medium, and cultured in an incubator at 37±1°C for 18 to 36 hours. After condensing the bacteria in the fermented bacteria liquid, use high temperature to heat to kill the bacteria. Finally, the protective agent is added and freeze-dried to make Lactobacillus reuteri GMNL-2632×10 per gram 10 Cells heat kills bacteria powder.
[0024] In addition, the following specific examples can further prove the scope of practical application of the present invention, but it is not intended to limit the scope of the present invention in any form.
[0025] First, 6-week-old weaned male hamsters of the malet strain were purchased from the National Laboratory Animal Center of Taiwan (Taipei, Taiwan), and were raised in plastic cages, 8 per group, 32 in ...
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[0035] Example 1: Analysis of the biochemical content of serum, liver and feces
[0036] Serum biochemical value analysis: The test items are the lipid concentration in the blood, including triglycerides (TG), total cholesterol (T-CHO), high-density lipoprotein cholesterol (HDL-CHO) and low-density lipoprotein cholesterol (LDL) -CHO), the above test items are all commissioned to analyze by the National Laboratory Animal Center of Taiwan, China.
[0037] Analysis of malonaldehyde (MDA) content in blood: Use the commercially available TBARS Assay Kit (Cayman) to determine the content of malonaldehyde in the serum. Refer to the manufacturer’s instructions for the experimental procedures, and finally analyze by disk spectroscopy at a wavelength of 530nm The instrument measures the absorbance, and calculates the cytokine content in the sample with the standard concentration curve.
[0038] Lipid analysis of liver and feces: Take 0.1g of the analyzed tissue and homogenize it in 1ml of chl...
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[0045] Example 2: Analysis of the effect of GMNL-263 heat-killing bacteria on mRNA gene expression in liver and adipose tissue
[0046] Use RT-PCR to detect (I) liver tissue and (II) adipose tissue mRNA gene expression. The detected genes are:
[0047] 1. Inflammation-promoting factors: interleukin-6 (IL-6) and tumor necrosis factor α (TNF-α), the expression of the above genes can cause inflammation.
[0048] 2. Lipid synthesis related genes: fatty acid synthase (FAS), cholesterol regulatory element binding protein (sterol response element binding protein-1, SREBP-1c), peroxisome proliferator activated receptor γ ( peroxisome prolifera proliferator-activated receptor gamma (PPAR gamma); among them, fatty acid synthase (FAS) and cholesterol regulatory element binding protein (SREBP-1c) genes are involved in the synthesis of fatty acids, and peroxisome proliferator activated receptor gamma (PPAR gamma) It is related to the metabolism of fatty acids.
[0049] 3. Genes related to cholest...
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