2022
DOI: 10.3389/fnut.2021.770264
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High Value-Added Application of Two Renewable Sources as Healthy Food: The Nutritional Properties, Chemical Compositions, Antioxidant, and Antiinflammatory Activities of the Stalks of Rheum officinale Baill. and Rheum tanguticum Maxim. ex Regel

Abstract: Rhubarb plants (Rheum officinale and R. tanguticum) have edible stalks. In this work, we aimed to compare the nutritional properties, chemical compositions, and bioactivities of R. officinale (SRO) and R. tanguticum (SRT) stalks and to analyze the composition–function relationship. Results showed that the two stalks were good sources of fiber, as well as minerals. They contained abundant essential amino acids and essential fatty acids to regulate the immunity and prevent some chronic diseases; the contents of … Show more

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Cited by 3 publications
(10 citation statements)
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“…The content of total phenolic compounds (TPCs) in LRO harvested in the different seasons was determined using the Folin–Ciocalteu method, and the results are expressed as mg of gallic acid equivalent/100 g of fresh sample (mg GAE/100 g). The content of flavonoids (TF) in LRO was measured according to the aluminum chloride colorimetric method, and the result was expressed as mg of quecertin/100 g of fresh sample (mg QE/100 g) ( 3 ). The absorbance was measured at a wavelength of 760 nm to determine the TPC and 510 nm to measure the TF.…”
Section: Methodsmentioning
confidence: 99%
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“…The content of total phenolic compounds (TPCs) in LRO harvested in the different seasons was determined using the Folin–Ciocalteu method, and the results are expressed as mg of gallic acid equivalent/100 g of fresh sample (mg GAE/100 g). The content of flavonoids (TF) in LRO was measured according to the aluminum chloride colorimetric method, and the result was expressed as mg of quecertin/100 g of fresh sample (mg QE/100 g) ( 3 ). The absorbance was measured at a wavelength of 760 nm to determine the TPC and 510 nm to measure the TF.…”
Section: Methodsmentioning
confidence: 99%
“…The in vitro antioxidant activity of LRO was investigated according to a previously described method ( 3 ). For the DPPH radical scavenging activity assay, LRO (50–1,000 μg/mL) was added to 96-well plates with a methanol solution of DPPH (100 μL, 0.2 mM) and then incubated at 37°C for 30 min in the dark.…”
Section: Methodsmentioning
confidence: 99%
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