Lactational metformin exposure programs offspring white adipose tissue glucose homeostasis and resilience to metabolic stress in a sex-dependent manner.
Zach CarlsonHannah HafnerMolly MulcahyKaylie BullockAllen ZhuDave E BridgesErnesto Bernal-MizrachiBrigid E GreggPublished in: American journal of physiology. Endocrinology and metabolism (2020)
We previously demonstrated that exposing mouse dams to metformin during gestation results in increased beta-cell mass at birth and increased beta-cell insulin secretion in adult male offspring. Given these favorable changes after a gestational maternal metformin exposure, we wanted to understand the long-term metabolic impact on offspring after exposing dams to metformin during the postnatal window. The newborn period provides a feasible clinical window for intervention and is important for beta-cell proliferation and metabolic tissue development. Using a C57BL/6 model, we administered metformin to dams from the day of birth to postnatal day 21. We monitored maternal health and offspring growth during the lactation window, as well as adult glucose homeostasis through in vivo testing. At necropsy we assessed pancreas and adipocyte morphology using histological and immunofluorescent staining techniques. We found that metformin exposure programmed male and female offspring to be leaner with a higher proportion of small adipocytes in the gonadal white adipose tissue (GWAT). Male, but not female, offspring had an improvement in glucose tolerance as young adults concordant with a mild increase in insulin secretion in response to glucose in vivo. These data demonstrate long-term metabolic programming of offspring associated with maternal exposure to metformin during lactation.
Keyphrases
- high fat diet
- adipose tissue
- insulin resistance
- young adults
- pregnancy outcomes
- preterm infants
- birth weight
- cell proliferation
- public health
- single cell
- healthcare
- blood glucose
- randomized controlled trial
- pregnant women
- cell cycle
- type diabetes
- human milk
- climate change
- skeletal muscle
- risk assessment
- metabolic syndrome
- blood pressure
- pi k akt
- dairy cows
- social support
- mesenchymal stem cells
- artificial intelligence
- social media
- childhood cancer
- electronic health record
- heat stress