Differential Effects of Foods Traditionally Regarded as ‘Heating’ and ‘Cooling’ on Prostaglandin E2 Production by a Macrophage Cell Line
Some components of natural foods may enhance or inhibit prostaglandin formation and potentially affect the inflammation condition. A macrophage cell line, RAW264.7, was employed to examine the effects of foods traditionally regarded as ‘heating’ or ‘cooling’ on the production of PGE 2 , a well-known...
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Veröffentlicht in: | Journal of biomedical science 2002-06, Vol.9 (6), p.596-606 |
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description | Some components of natural foods may enhance or inhibit prostaglandin formation and potentially affect the inflammation condition. A macrophage cell line, RAW264.7, was employed to examine the effects of foods traditionally regarded as ‘heating’ or ‘cooling’ on the production of PGE 2 , a well-known proinflammatory mediator. Foods traditionally regarded as ‘heating’ (litchi, longan, and dried longan) or ‘cooling’ (chrysanthemum flower, bitter gourd, and lotus seed plumule) were extracted sequentially with water and ethyl acetate. The water extracts (WE) and ethyl acetate extracts (EAE) were applied to RAW264.7 macrophages in the presence or absence of LPS (lipopolysaccharide). In the absence of LPS, the WEs from the ‘heating foods’, litchi, longan, or dried longan had a dose-dependent enhancing effect on PGE 2 production, with respective EC 50 s of 8.4, 16, and 11 mg/ml. This effect was accompanied by significant induction of COX-2 protein expression, as shown by Western blot analysis. In contrast, LPS-induced PGE 2 production was inhibited in a dose-dependent manner by the WEs of the ‘cooling foods’, chrysanthemum flower, bitter gourd, and lotus seed plumule, with respective IC 50 s of 0.6, 0.13, and 0.08 mg/ml. At the concentrations tested, none of the EAEs had any effect on basal PGE 2 production, while LPS-induced PGE 2 production was inhibited or increased by the EAE from bitter gourd and longan, respectively. Water-soluble extracts of foods traditionally regarded as ‘heating’ enhanced basal PGE 2 production, while those from ‘cooling’ foods significantly inhibited LPS-induced PGE 2 production by the macrophage cell line. This subject merits further study to determine whether appropriate food selection may help patients suffering from chronic inflammatory conditions. |
doi_str_mv | 10.1159/000067288 |
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A macrophage cell line, RAW264.7, was employed to examine the effects of foods traditionally regarded as ‘heating’ or ‘cooling’ on the production of PGE 2 , a well-known proinflammatory mediator. Foods traditionally regarded as ‘heating’ (litchi, longan, and dried longan) or ‘cooling’ (chrysanthemum flower, bitter gourd, and lotus seed plumule) were extracted sequentially with water and ethyl acetate. The water extracts (WE) and ethyl acetate extracts (EAE) were applied to RAW264.7 macrophages in the presence or absence of LPS (lipopolysaccharide). In the absence of LPS, the WEs from the ‘heating foods’, litchi, longan, or dried longan had a dose-dependent enhancing effect on PGE 2 production, with respective EC 50 s of 8.4, 16, and 11 mg/ml. This effect was accompanied by significant induction of COX-2 protein expression, as shown by Western blot analysis. In contrast, LPS-induced PGE 2 production was inhibited in a dose-dependent manner by the WEs of the ‘cooling foods’, chrysanthemum flower, bitter gourd, and lotus seed plumule, with respective IC 50 s of 0.6, 0.13, and 0.08 mg/ml. At the concentrations tested, none of the EAEs had any effect on basal PGE 2 production, while LPS-induced PGE 2 production was inhibited or increased by the EAE from bitter gourd and longan, respectively. Water-soluble extracts of foods traditionally regarded as ‘heating’ enhanced basal PGE 2 production, while those from ‘cooling’ foods significantly inhibited LPS-induced PGE 2 production by the macrophage cell line. 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A macrophage cell line, RAW264.7, was employed to examine the effects of foods traditionally regarded as ‘heating’ or ‘cooling’ on the production of PGE 2 , a well-known proinflammatory mediator. Foods traditionally regarded as ‘heating’ (litchi, longan, and dried longan) or ‘cooling’ (chrysanthemum flower, bitter gourd, and lotus seed plumule) were extracted sequentially with water and ethyl acetate. The water extracts (WE) and ethyl acetate extracts (EAE) were applied to RAW264.7 macrophages in the presence or absence of LPS (lipopolysaccharide). In the absence of LPS, the WEs from the ‘heating foods’, litchi, longan, or dried longan had a dose-dependent enhancing effect on PGE 2 production, with respective EC 50 s of 8.4, 16, and 11 mg/ml. This effect was accompanied by significant induction of COX-2 protein expression, as shown by Western blot analysis. In contrast, LPS-induced PGE 2 production was inhibited in a dose-dependent manner by the WEs of the ‘cooling foods’, chrysanthemum flower, bitter gourd, and lotus seed plumule, with respective IC 50 s of 0.6, 0.13, and 0.08 mg/ml. At the concentrations tested, none of the EAEs had any effect on basal PGE 2 production, while LPS-induced PGE 2 production was inhibited or increased by the EAE from bitter gourd and longan, respectively. Water-soluble extracts of foods traditionally regarded as ‘heating’ enhanced basal PGE 2 production, while those from ‘cooling’ foods significantly inhibited LPS-induced PGE 2 production by the macrophage cell line. 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A macrophage cell line, RAW264.7, was employed to examine the effects of foods traditionally regarded as ‘heating’ or ‘cooling’ on the production of PGE 2 , a well-known proinflammatory mediator. Foods traditionally regarded as ‘heating’ (litchi, longan, and dried longan) or ‘cooling’ (chrysanthemum flower, bitter gourd, and lotus seed plumule) were extracted sequentially with water and ethyl acetate. The water extracts (WE) and ethyl acetate extracts (EAE) were applied to RAW264.7 macrophages in the presence or absence of LPS (lipopolysaccharide). In the absence of LPS, the WEs from the ‘heating foods’, litchi, longan, or dried longan had a dose-dependent enhancing effect on PGE 2 production, with respective EC 50 s of 8.4, 16, and 11 mg/ml. This effect was accompanied by significant induction of COX-2 protein expression, as shown by Western blot analysis. In contrast, LPS-induced PGE 2 production was inhibited in a dose-dependent manner by the WEs of the ‘cooling foods’, chrysanthemum flower, bitter gourd, and lotus seed plumule, with respective IC 50 s of 0.6, 0.13, and 0.08 mg/ml. At the concentrations tested, none of the EAEs had any effect on basal PGE 2 production, while LPS-induced PGE 2 production was inhibited or increased by the EAE from bitter gourd and longan, respectively. Water-soluble extracts of foods traditionally regarded as ‘heating’ enhanced basal PGE 2 production, while those from ‘cooling’ foods significantly inhibited LPS-induced PGE 2 production by the macrophage cell line. This subject merits further study to determine whether appropriate food selection may help patients suffering from chronic inflammatory conditions.</abstract><cop>Basel, Switzerland</cop><pmid>12432225</pmid><doi>10.1159/000067288</doi><tpages>11</tpages></addata></record> |
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title | Differential Effects of Foods Traditionally Regarded as ‘Heating’ and ‘Cooling’ on Prostaglandin E2 Production by a Macrophage Cell Line |
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