Melatonin attenuates prenatal dexamethasone-induced blood pressure increase in a rat model

• DOI: 10.1016/j.jash.2014.01.009
• Publication Date: 2014-02-06T21:16:54Z
• Authors: You-Lin Tain; Chih-Cheng Chen; Jiunn-Ming Sheen; Hong-Ren Yu; Mao-Meng Tiao; Ho-Chang Kuo; Li-Tung Huang
• Keywords: 0301 basic medicine; Blotting, Western; Receptors, Cell Surface; Nitric Oxide; Real-Time Polymerase Chain Reaction; Proto-Oncogene Mas; Dexamethasone; Histone Deacetylases; Rats; Receptors, G-Protein-Coupled; 3. Good health; Rats, Sprague-Dawley; 03 medical and health sciences; Maternal Exposure; Pregnancy; Prenatal Exposure Delayed Effects; Proto-Oncogene Proteins; Hypertension; Renin; Animals; Female; RNA, Messenger; Melatonin

Although antenatal corticosteroid is recommended to accelerate fetal lung maturation, prenatal dexamethasone exposure results in hypertension in the adult offspring. Since melatonin is a potent antioxidant and has been known to regulate blood pressure, we examined the beneficial effects of melatonin therapy in preventing prenatal dexamethasone-induced programmed hypertension. Male offspring of Sprague-Dawley rats were assigned to four groups (n = 12/group): control, dexamethasone (DEX), control + melatonin, and DEX + melatonin. Pregnant rats received intraperitoneal dexamethasone (0.1 mg/kg) from gestational day 16 to 22. In the melatonin-treatment groups, rats received 0.01% melatonin in drinking water during their entire pregnancy and lactation. Blood pressure was measured by an indirect tail-cuff method. Gene expression and protein levels were analyzed by real-time quantitative polymerase chain reaction and Western blotting, respectively. At 16 weeks of age, the DEX group developed hypertension, which was partly reversed by maternal melatonin therapy. Reduced nephron numbers due to prenatal dexamethasone exposure were prevented by melatonin therapy. Renal superoxide and NO levels were similar in all groups. Prenatal dexamethasone exposure led to increased mRNA expression of renin and prorenin receptor and up-regulated histone deacetylase (HDAC)-1 expression in the kidneys of 4-month-old offspring. Maternal melatonin therapy augmented renal Mas protein levels in DEX + melatonin group, and increased renal mRNA expression of HDAC-1, HDAC-2, and HDAC-8 in control and DEX offspring. Melatonin attenuated prenatal DEX-induced hypertension by restoring nephron numbers, altering RAS components, and modulating HDACs.