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.