Application of atractylenolide I in preparation of medicine for protecting embryonic development of pregnancy complicated with diabetes mellitus
A technology of atractylodes lactone and embryonic development, which is applied in the direction of drug combination, disease, metabolic disease, etc., to achieve the effect of improving application value and expanding application range
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Embodiment 1
[0063] A certain concentration of atractyloid Ⅰ will not affect embryonic development
[0064] In order to determine whether Atractylolide Ⅰ has cytotoxic effect on embryonic development, early chick embryos were cultured by the method of Early chick Culture (EC Culture). The inventor added physiological saline in the culture medium as a control group; the final concentration of Atractylodes lactone I in the culture medium in the experimental group was 7.5 μM, 15 μM, and 30 μM respectively, and the chicken embryos of stage 0 (HH0) were incubated and harvested in 36 hours ( figure 2 A). Using the length of the embryo and the number of somites (the landmark structure for judging the early development stage of chicken embryos), the inventors found that 7.5 μM and 15 μM Atractylodes lactone Ⅰ had no significant effect on the development of chicken embryos, but 30 μM Atractylodes lactone Ⅰ The treatment significantly reduced the length of embryo development and the number of somi...
Embodiment 2
[0067] Atractylodes lactone Ⅰ can significantly improve embryonic death and developmental deformity induced by high glucose environment
[0068] Based on the chicken embryo model of gestational diabetes established by the inventor (Cell Cycle: 14(5):772-783.2015), the inventor set up a chicken embryo control group (normal saline), a high-sugar group (50mM glucose), and atractylodes lactone I low Concentration group (50mM glucose + 7.5μM Atractylodes lactone Ⅰ), atractylodes lactone Ⅰ medium concentration group (50mM glucose + 15μM Atractylodes lactone Ⅰ) a total of 4 groups, chicken embryos were cultured in the 4 groups of EC Culture to HH10 stage for development Statistics of period and deformity rate. The inventors compared the development of gastrula chick embryos exposed to normal saline, high sugar, and / or 7.5 μM and 15 μM Atractylodes lactone Ⅰ at the 36th hour of chicken embryo development ( image 3 A), the inventor found that the high-sugar environment can affect emb...
Embodiment 3
[0071] Atractylactone Ⅰ improves embryonic vascular failure caused by high glucose
[0072] The inventors used the chicken embryo YSM (yolk sac membrane) model to study whether Atractylolide Ⅰ can protect angiogenesis from being inhibited by high glucose (50mM glucose) ( Figure 4 A-D). The inventor set up a chicken embryo control group (normal saline), a high-sugar group (50mM glucose), atractylactone Ⅰ group (15μM atractylactone Ⅰ), a high-sugar + atractylactone Ⅰ group (50mM glucose+15μM atractylactone Ⅰ ) a total of 4 groups, incubate 0-day fertilized eggs for 2.5 days, take the rubber ring and stick it on the YSM, add the above solution to the rubber ring of the chicken embryo YSM in groups. After further culturing for 36 hours, the inventors found that compared with the angiogenesis of YSM in the control group ( Figure 4 A1-D1), the blood vessel density in the high glucose group was significantly reduced (P Figure 4 E), the blood vessel density of the 15 μM atractyloi...
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