PT - JOURNAL ARTICLE AU - Antje Kaufhold AU - Prabhat K. Nigam AU - Ravindra N. Dhir AU - Bernard H. Shapiro TI - Prevention of Latently Expressed CYP2C11, CYP3A2, and Growth Hormone Defects in Neonatally Monosodium Glutamate-Treated Male Rats by the <em>N</em>-Methyl-<span class="sc">d</span>-Aspartate Receptor Antagonist Dizocilpine Maleate AID - 10.1124/jpet.102.034785 DP - 2002 Aug 01 TA - Journal of Pharmacology and Experimental Therapeutics PG - 490--496 VI - 302 IP - 2 4099 - http://jpet.aspetjournals.org/content/302/2/490.short 4100 - http://jpet.aspetjournals.org/content/302/2/490.full SO - J Pharmacol Exp Ther2002 Aug 01; 302 AB - Neonatal administration of monosodium glutamate (MSG) can produce latently expressed defects in drug metabolism and growth hormone secretion as well as stunted growth and obesity. Instead of secreting growth hormone in the masculine episodic profile, plasma hormone levels are generally undetectable in affected adult male rats. Moreover, male-specific isoforms of cytochrome P450 (P450; e.g., CYP2C11 and CYP3A2), whose combined levels comprise the bulk of the total hepatic P450 in adult male rats, are similarly undetectable in these animals. Since “signaling elements” in the masculine episodic growth hormone profile are solely responsible for the elevated characteristic male-like expression levels of CYP2C11 and CYP3A2, suppression of the isoforms in the MSG-treated rats appeared to be caused by the simple absence of the hormone from the circulation. However, the reported failures of restored physiologic masculine growth hormone profiles to correct the P450 defects suggested the occurrence of direct MSG-induced liver damage independent of the well known hypothalamic lesions produced by the amino acid. Concurrent administration of dizocilpine maleate (MK-801), a selective and highly potent noncompetitive N-methyl-d-aspartate receptor antagonist of glutamate, completely prevented the adverse effects of neonatal MSG treatment on P450 expression, growth hormone secretion, and growth parameters, indicating that the amino acid-induced defects are solely a result of neuronal (i.e., hypothalamic) damage produced at the time of MSG exposure. The irreversibility of the P450 damage is described as resulting from secondary defects initially induced by the neuronal lesions. The American Society for Pharmacology and Experimental Therapeutics