2018
DOI: 10.1016/j.foodchem.2018.01.093
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Purification and identification of anti-inflammatory peptides from spent hen muscle proteins hydrolysate

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Cited by 62 publications
(34 citation statements)
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“…Compared with protein hydrolysates from other meat byproducts such as skin, bone, viscera, blood and sarcoplasmic proteins, SPHs appeared to have a more potent ACE inhibitory activity (IC 50 values of 23–189 μg/mL) [ 50 , 51 , 52 , 53 , 54 ]. The extracted proteins in this study contained mainly myofibrillar proteins as reported previously [ 29 , 30 ]. The major protein bands include myosin heavy chain (~220 kDa), actin (42 kDa), and myosin light chain (15–25 kDa) ( Figure 1 A) [ 37 , 55 , 56 ].…”
Section: Discussionmentioning
confidence: 99%
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“…Compared with protein hydrolysates from other meat byproducts such as skin, bone, viscera, blood and sarcoplasmic proteins, SPHs appeared to have a more potent ACE inhibitory activity (IC 50 values of 23–189 μg/mL) [ 50 , 51 , 52 , 53 , 54 ]. The extracted proteins in this study contained mainly myofibrillar proteins as reported previously [ 29 , 30 ]. The major protein bands include myosin heavy chain (~220 kDa), actin (42 kDa), and myosin light chain (15–25 kDa) ( Figure 1 A) [ 37 , 55 , 56 ].…”
Section: Discussionmentioning
confidence: 99%
“…All three SPHs inhibited expression of VCAM-1 ( p < 0.05) to a similar extent but did not affect that of ICAM-1 in TNFα-induced EA.hy926 cells. Hydrolysates or peptides with anti-inflammatory effects have been prepared from various food commodities such as meat, zein, beans and egg white, some of which have further been validated their physiological efficacy in animals [ 9 , 29 , 34 , 47 , 65 , 66 ]. Next, we studied the effects of simulated gastrointestinal and transport digestions on the activities of SPH-T, SPH-26L, and SPH-P.…”
Section: Discussionmentioning
confidence: 99%
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“…Spent laying hen carcasses were obtained from a local supermarket (Edmonton, AB, Canada). Hen protein hydrolysate (HPH) was prepared according to the method to purify bioactive peptides as described by Yu, Field, and Wu (). Briefly, after pre‐heating to 90 °C at pH 5.0 for 10 min, the pH of spent hen protein mince was maintained at pH 3.0 using a Titrando instrument (Metrohm, Herisan, Switzerland), and Protex 50FP (Genencor International Inc., Rochester, NY, USA) enzyme was added at 4% (w/w, mixed with distilled water) and incubated for 180 min at 50 °C.…”
Section: Methodsmentioning
confidence: 99%