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. 2018 Mar 9;38(2):BSR20171741. doi: 10.1042/BSR20171741

Table 1. Relevant studies about maternal resveratrol intake and metabolic health in offspring.

Resveratrol consumption Intervention period Species Beneficial effects on pregnant females Beneficial effects on offspring Potential mechanism References
A Western-style diet supplemented with 0.37% resveratrol Throughout pregnancy Nonhuman primates - Resulted in maternal weight loss and improved glucose tolerance - Fetal pancreatic mass was enlarged by 42% May be driven by an eNOS-dependent mechanism Roberts et al. [43]
- Increased uterine artery volume blood flow - A 12-fold increase in proliferation
- Decreased placental inflammation and liver triglyceride deposition
Oral gavage with resveratrol (10 mg/kg body weight per day) Four weeks before pregnancy and during pregnancy A genetic GDM model: C57BL/KsJ-Leptin (db/+) mouse - Improved glucose metabolism, insulin tolerance, and reproductive outcome of the pregnant db/+ females - Increased fetal survival and decreased body weight - Enhanced AMPK activation Yao et al. [44]
- Reduced production and activity of G6Pase
50, 100, and 200 μmol/l resveratrol incubation 6- and/or 24-h incubation Human placenta - Quenched inflammation induced by LPS NA - SIRT1 possessed anti-inflammatory actions Lappas et al. [45]
200 μmol/l resveratrol incubation 20-h incubation Human placenta, adipose tissue, and skeletal muscle - Reduced the expression and secretion of pro-inflammatory cytokines IL-6, IL-1α, IL-1β, IL-8, and MCP-1 in human placenta and omental and subcutaneous adipose tissue NA - Restored the impaired insulin signaling pathway and insulin-mediated glucose uptake in human skeletal muscle Tran et al. [46]
A high-fat diet with or without 0.2% (w/w) resveratrol During pregnancy and lactation C57BL/6 J mice - Protected dams against body weight gain and fat accumulation - Increased energy expenditure and insulin sensitivity - Increased phosphorylated AMPKα levels, Sirt1, PRDM16, and other thermogenic genes protein contents Zou et al. [47]
- Reduced the concentrations of triglycerides and insulin - Enhanced white adipose tissue browning
Resveratrol (50 mg/l) in drinking water During pregnancy and lactation Wistar rats - No difference in body weight at the end of lactation - Reduced body weight, leptin, VAT and SCAT, with females being more affected - Decreased fatty acid synthase expression in VAT Ros et al. [48]
- An antiadipogenic effect
Resveratrol (30 mg/kg body weight/day) 8 weeks before mating and throughout gestation and lactation Wistar rats NA - Decreased body weight, subcutaneous and visceral fat mass, and adiposity - Increased p-STAT3 content in the hypothalamus Franco et al. [49]
Resveratrol (100 mg/kg body weight) was administered by gavage feeding 10 days (from day E3 to E12) Sprague Dawley rats - Decreased lipid accumulation including cholesterol by 41.74% and triglyceride by 60.64% and increased HDL in diabetic dams - Prevented both oxidative stress and apoptosis in embryos - Stimulation of the extrinsic and intrinsic pathway Singh et al. [50]
- May attenuate the expression of HMG-CoA reductase
Resveratrol-supplemented diet (4 g/kg diet) From gestational day 0.5 until postnatal day 21 Spontaneously hypertensive rat - Had no effect on blood flow patterns in the maternal uterine arteries - Mitigated the development of hypertension in adult offspring - Improved nitric oxide bioavailability Care et al. [51]
20 mg/kg per day and twice daily During the whole pregnancy Wistar albino rats - Did not decrease blood pressure NA NA Moraloglu et al. [52]
- No changes in blood flows and placental pathology parameters
Resveratrol supplementation (4 g/kg diet) For 9 weeks following weaning Sprague–Dawley rats NA - Improved cardiac recovery from ischemia/reperfusion injury - Unclear, without AMPK–ACC signaling activation Shah et al. [53]
- Attenuated superoxide levels

Abbreviations: ACC, acetyl-CoA carboxylase; AMPK, adenosine monophosphate activated protein kinase; E, embryonic; eNOS, endothelial nitric oxide synthase; G6Pase, glucose-6-phosphatase; GDM:, gestational diabetes mellitus; HDL, high-density lipoprotein; HMG-CoA, hydroxy-3-methyl-glutaryl (HMG)-CoA reductase; IL-1α, interleukin-1α; IL-1β, interleukin-1β; IL-6, interleukin-6; IL-8, interleukin-8; LPS, lipopolysaccharide; MCP-1, monocyte chemoattractantprotein-1; NA, not available; PRDM16, PR domain containing 16; p-STAT3, phosphorylated-signal transducer and activator of transcription 3; SCAT, subcutaneous adipose tissue; SIRT, sirtuin; VAT, visceral adipose tissue.