Gut Microbiota Perturbation in Early Life Could Influence Pediatric Blood Pressure Regulation in a Sex-Dependent Manner in Juvenile Rats.
Yang YangJinxing LiZhimo ZhouSimou WuJincheng ZhaoWen JiaMeixun LiuXi ShenFang HeRuYue ChengPublished in: Nutrients (2023)
The present study aimed to investigate whether gut dysbiosis induced by ceftriaxone in early life could influence pediatric blood pressure regulation in childhood with or without exposure to a high-fat diet (HFD). Sixty-three newborn pups of Sprague-Dawley rats were administered ceftriaxone sodium or saline solution until weaning at 3 weeks, and the rats were fed a HFD or regular diet from 3 to 6 weeks. Tail-cuff blood pressure, the expression levels of genes of the renin-angiotensin system (RAS), the concentrations of IL-1β, IL-6, and TNF-α in the colon and prefrontal cortex, and the composition of fecal microbiota were analyzed. Ceftriaxone treatment significantly increased the diastolic blood pressure of male rats at 3 weeks. At 6 weeks, systolic blood pressure (SBP) was significantly increased only in ceftriaxone treated male rats fed with HFD. The RAS showed increased activation in the kidney, heart, hypothalamus, and thoracic and abdominal aorta of male rats, but only in the kidney, heart, and hypothalamus of female rats. HFD-fed female rats showed a decreased level of IL-6 in the colon. α diversity of gut microbiota decreased and the Firmicutes to Bacteroidetes ratio increased in both male and female rats at 3 weeks; however, these parameters recovered to various degrees in female rats at 6 weeks. These results revealed that early-life gut dysbiosis induced by antibiotics combined with a HFD in childhood could be involved in pediatric blood pressure regulation and an increase in SBP in juvenile rats, and these effects occurred in a sex-dependent manner.
Keyphrases
- blood pressure
- early life
- high fat diet
- hypertensive patients
- insulin resistance
- adipose tissue
- heart rate
- gestational age
- prefrontal cortex
- heart failure
- rheumatoid arthritis
- left ventricular
- blood glucose
- skeletal muscle
- young adults
- spinal cord injury
- mechanical ventilation
- physical activity
- single cell
- gene expression
- intensive care unit
- transcription factor
- metabolic syndrome
- binding protein
- acute respiratory distress syndrome
- childhood cancer