2013
DOI: 10.1016/j.jnutbio.2013.08.003
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Grape skin extract protects against programmed changes in the adult rat offspring caused by maternal high-fat diet during lactation

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Cited by 48 publications
(84 citation statements)
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“…Different studies have shown that the administration of polyphenols to dams during prenatal and early postnatal periods can exert beneficial effects on body fat gain and different metabolic disorders, such us dyslipidaemia, insulin resistance and inflammation, on their offspring in later life [15][16][17]19]. However, in most of these studies, the metabolic programming effects of polyphenols have been observed after the administration of these compounds at high doses.…”
Section: Discussionmentioning
confidence: 99%
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“…Different studies have shown that the administration of polyphenols to dams during prenatal and early postnatal periods can exert beneficial effects on body fat gain and different metabolic disorders, such us dyslipidaemia, insulin resistance and inflammation, on their offspring in later life [15][16][17]19]. However, in most of these studies, the metabolic programming effects of polyphenols have been observed after the administration of these compounds at high doses.…”
Section: Discussionmentioning
confidence: 99%
“…We recently demonstrated that these bioactive food compounds can reach the foetuses and placentas of pregnant rats [11]. Furthermore, recent studies have shown that polyphenols can exert metabolic programming effects on the offspring through maternal intake [12][13][14][15][16][17][18][19][20]. For example, genistein was effective in preventing body weight gain of the offspring when administered during pregnancy and lactation [12,14] but also exerted harmful effects related to anxiety, aggressive behaviours, spatial learning and reproductive development [13,14].…”
Section: Introductionmentioning
confidence: 99%
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“…Since cardiovascular phenotypes often develop after a prolonged asymptomatic phase in childhood and for the sake of brevity, we have restricted this review to data obtained from adult offspring. Here we summarize in Table 1 studies documenting cardiovascular programming related to oxidative stress [43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68]. …”
Section: Impact Of Oxidative Stress On Cardiovascular Programming mentioning
confidence: 99%
“…A number of early-life insults have been reported to cause cardiovascular programming related to oxidative stress, including undernutrition [43,48,51,54,55,61,63,64], streptozotocin (STZ)-induced diabetes [44,62], preeclampsia [45,46,47], prenatal hypoxia [49,56], maternal nicotine exposure [59,60], ethanol consumption [50], maternal inflammation [57], prenatal glucocorticoid exposure [52,53,65,67,68], and maternal high-fat intake [58,66]. Limited information is available using large animals to study oxidative stress and cardiovascular programming simultaneously [67,68].…”
Section: Impact Of Oxidative Stress On Cardiovascular Programming mentioning
confidence: 99%