PMID- 24764457 OWN - NLM STAT- PubMed-not-MEDLINE DCOM- 20140425 LR - 20211021 IS - 1476-9255 (Print) IS - 1476-9255 (Electronic) IS - 1476-9255 (Linking) VI - 10 DP - 2013 TI - Prenatal exposure to lipopolysaccharide results in myocardial remodelling in adult murine offspring. PG - 35 LID - 10.1186/1476-9255-10-35 [doi] AB - BACKGROUND: The epigenetic plasticity hypothesis indicates that pregnancy exposure may result in adult-onset diseases, including hypertension, diabetes and cardiovascular disease, in offspring. In a previous study, we discovered that prenatal exposure to inflammatory stimulants, such as lipopolysaccharides (LPS), could lead to hypertension in adult rat offspring. In the present study, we further demonstrate that maternal inflammation induces cardiac hypertrophy and dysfunction via ectopic over-expression of nuclear transcription factor kappaB (NF- kappaB), and pyrrolidine dithiocarbamate (PDTC) can protect cardiac function by reducing maternal inflammation. METHODS: Pregnant SD rats were randomly divided into three groups and intraperitoneally injected with a vehicle, LPS (0.79 mg/kg), or LPS (0.79 mg/kg) plus PDTC (100 mg/kg) at 8 to 12 days of gestation. The offspring were raised until 4 and 8 months old, at which point an echocardiographic study was performed. The left ventricular (LV) mass index and apoptosis were examined. RESULTS: At 4 months of age, the LPS offspring exhibited augmented posterior wall thickness. These rats displayed left ventricle (LV) hypertrophy and LV diastolic dysfunction as well as a higher apoptotic index, a higher level of Bax and a lower level of Bcl-2 at 8 months of age. The protein levels of NF-kappaB (p65) in the myocardium of the offspring were measured at this time. NF-kappaB protein levels were higher in the myocardium of LPS offspring. The offspring that were prenatally treated with PDTC displayed improved signs of blood pressure (BP) and LV hypertrophy. CONCLUSIONS: Maternal inflammation can induce cardiac hypertrophy in offspring during aging accompanied with hypertension emergence and can be rescued by the maternal administration of PDTC (the inhibitor of NF-kappaB). FAU - Wei, Yanling AU - Wei Y AD - The Institute of Materia Medica and Department of Pharmaceutics, College of Pharmacy, The Third Military Medical University, Chongqing, China ; Department of Gastroenterology, Research Institute of Surgery, Da ping Hospital, The Third Military Medical University, Chongqing, China. FAU - Du, Wenhua AU - Du W AD - Department of Ultrasound, Research Institute of Surgery, Da ping Hospital, The Third Military Medical University, Chongqing, China. FAU - Xiong, Xiuqin AU - Xiong X AD - Department of Ultrasound, Research Institute of Surgery, Da ping Hospital, The Third Military Medical University, Chongqing, China. FAU - He, Xiaoyan AU - He X AD - The Institute of Materia Medica and Department of Pharmaceutics, College of Pharmacy, The Third Military Medical University, Chongqing, China. FAU - Ping Yi AU - Ping Yi AD - Department of Gynaecology, Research Institute of Surgery, Da ping Hospital, The Third Military Medical University, Chongqing, China. FAU - Deng, Youcai AU - Deng Y AD - The Institute of Materia Medica and Department of Pharmaceutics, College of Pharmacy, The Third Military Medical University, Chongqing, China. FAU - Chen, Dongfeng AU - Chen D AD - Department of Gastroenterology, Research Institute of Surgery, Da ping Hospital, The Third Military Medical University, Chongqing, China. FAU - Li, Xiaohui AU - Li X AD - The Institute of Materia Medica and Department of Pharmaceutics, College of Pharmacy, The Third Military Medical University, Chongqing, China. LA - eng PT - Journal Article DEP - 20131119 PL - England TA - J Inflamm (Lond) JT - Journal of inflammation (London, England) JID - 101232234 PMC - PMC3874617 OTO - NOTNLM OT - Foetal development OT - Inhibitor of NF-kappaB OT - Maternal inflammation OT - Myocardial remodelling EDAT- 2013/01/01 00:00 MHDA- 2013/01/01 00:01 PMCR- 2013/11/19 CRDT- 2014/04/26 06:00 PHST- 2012/10/05 00:00 [received] PHST- 2013/11/14 00:00 [accepted] PHST- 2014/04/26 06:00 [entrez] PHST- 2013/01/01 00:00 [pubmed] PHST- 2013/01/01 00:01 [medline] PHST- 2013/11/19 00:00 [pmc-release] AID - 1476-9255-10-35 [pii] AID - 10.1186/1476-9255-10-35 [doi] PST - epublish SO - J Inflamm (Lond). 2013 Nov 19;10:35. doi: 10.1186/1476-9255-10-35. eCollection 2013.