Physiological and behavioral responses in offspring mice following maternal exposure to sulfamonomethoxine during pregnancy

Neurosci Lett. 2016 Jun 15:624:8-16. doi: 10.1016/j.neulet.2016.05.007. Epub 2016 May 9.

Abstract

Sulfamonomethoxine (SMM), a veterinary antibiotic, is widely used in China. However, the impacts of maternal SMM exposure on neurobehavioral development in early life remain little known. In this study, we investigated the effects of maternal SMM exposure during pregnancy on behavioral and physiological responses in offspring mice. Pregnant mice were randomly divided into three SMM-treated groups, namely low-(10mg/kg/day), medium-(50mg/kg/day), and high-dose (200mg/kg/day), and a control group. The pregnant mice in the SMM-treated groups received SMM by gavage daily from gestational day 1-18, whereas those in the control received normal saline. On postnatal day (PND) 50, spatial memory was assessed using the Morris water maze test, and anxiety was measured using the elevated plus-maze and open field tests. The results showed significantly increased blood glucose in pups whose mothers received a high SMM dose. In addition, maternal SMM exposure increased anxiety-related activities among the offspring; spatial learning and memory were impaired more severely in the male offspring. The contents of tetrahydrobiopterin (BH4) and brain-derived neurotrophic factors (BDNF) on PND 22 were significantly reduced in the male offspring of the high-dose group compared with the controls. These findings indicate that SMM may be identified as a risk factor for cognitive and behavioral development on the basis of gender and that it may be associated with diminished BH4 and BDNF levels early in life.

Keywords: Anxiety; Maternal exposure; Offspring mice; Spatial cognition; Sulfamonomethoxine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Infective Agents / toxicity*
  • Anxiety / chemically induced
  • Behavior, Animal / drug effects
  • Blood Glucose
  • Body Weight / drug effects
  • Brain-Derived Neurotrophic Factor / blood
  • Female
  • Male
  • Maternal Exposure*
  • Maze Learning / drug effects
  • Mice
  • Mice, Inbred ICR
  • Pregnancy
  • Prenatal Exposure Delayed Effects / blood
  • Prenatal Exposure Delayed Effects / physiopathology*
  • Prenatal Exposure Delayed Effects / psychology*
  • Serotonin / blood
  • Sulfamonomethoxine / toxicity*
  • Thyroxine / blood
  • Triiodothyronine / blood

Substances

  • Anti-Infective Agents
  • Blood Glucose
  • Brain-Derived Neurotrophic Factor
  • Triiodothyronine
  • Serotonin
  • Thyroxine
  • Sulfamonomethoxine