2008
DOI: 10.1016/j.bbrc.2008.06.015
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Petalonia improves glucose homeostasis in streptozotocin-induced diabetic mice

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Cited by 31 publications
(21 citation statements)
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“…Recently, we demonstrated that an ethanolic extract of P. binghamiae (PBE) exerts an adipogenic effect in 3T3-L1 cells and an anti-diabetic effect in streptozotocin-induced diabetic mice [22]. However, this study revealed that the water-soluble extract of P. binghamiae (PBEE) exerts an anti-adipogenic effect in 3T3-L1 cells.…”
Section: Discussionmentioning
confidence: 87%
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“…Recently, we demonstrated that an ethanolic extract of P. binghamiae (PBE) exerts an adipogenic effect in 3T3-L1 cells and an anti-diabetic effect in streptozotocin-induced diabetic mice [22]. However, this study revealed that the water-soluble extract of P. binghamiae (PBEE) exerts an anti-adipogenic effect in 3T3-L1 cells.…”
Section: Discussionmentioning
confidence: 87%
“…In this regard, we have evaluated the potential of several extracts of the edible seaweed P. binghamiae in vitro using murine 3T3-L1 preadipocytes and in vivo using animal models [22]. In this study, we found that a water-soluble P. binghamiae extract, designated PBEE, dose dependently decreased the levels of triglycerides, PPARγ1 and 2, C/EBPα and aP2 in differentiating 3T3-L1 preadipocytes.…”
Section: Discussionmentioning
confidence: 93%
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“…There are also a few trials with seaweeds or seaweed preparations in humans investigating effects on blood pressure [5,6], appetite [7,8], inflammation [9], and insulin response [10]. These health effects may originate from a variety of seaweed compounds, such as soluble fiber and carotenoids [6,[11][12][13][14][15]. Only one study has so far shown which compounds can be used as biomarkers of seaweed intake in overweight or obese subjects.…”
Section: Introductionmentioning
confidence: 99%
“…Chlorella and Petalonia exhibited antidiabetic effects via both insulin-like and insulin-sensitizing behavior on in vitro tests (Cherng & Shih, 2006;Kang et al, 2008). The ethanolic extract of Ascophyllum nodosum inhibited rat-intestinal a-glucosidase, with an IC 50 value of 77 mg/ml and stimulated the reduction in liver glycogen levels in diabetic mice (Zhang et al, 2007).…”
Section: A-glucosidase and A-amylase Inhibitory Activitymentioning
confidence: 99%