Histamine N-methyltransferase regulates aggression and the sleep-wake cycle

• Published in: Scientific reports Vol. 7; no. 1; pp. 15899 - 9
• Main Authors: Naganuma, Fumito, Nakamura, Tadaho, Yoshikawa, Takeo, Iida, Tomomitsu, Miura, Yamato, Kárpáti, Anikó, Matsuzawa, Takuro, Yanai, Atushi, Mogi, Asuka, Mochizuki, Takatoshi, Okamura, Nobuyuki, Yanai, Kazuhiko
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 21.11.2017; Nature Publishing Group
• Subjects: 631/378/1385/1877; 631/378/1457/3918; 64/110; Aggression; Aggressive behavior; Aggressiveness; Biting; Central nervous system; Histamine; Histamine N-methyltransferase; Humanities and Social Sciences; Inactivation; Mental disorders; Methyltransferase; multidisciplinary; N-Methyltransferase; Physiology; Pyrilamine; Rodents; Science; Science (multidisciplinary); Sleep; Sleep and wakefulness
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-017-16019-8

Histamine is a neurotransmitter that regulates diverse physiological functions including the sleep-wake cycle. Recent studies have reported that histaminergic dysfunction in the brain is associated with neuropsychiatric disorders. Histamine N -methyltransferase (HNMT) is an enzyme expressed in the central nervous system that specifically metabolises histamine; yet, the exact physiological roles of HNMT are unknown. Accordingly, we phenotyped Hnmt knockout mice (KO) to determine the relevance of HNMT to various brain functions. First, we showed that HNMT deficiency enhanced brain histamine concentrations, confirming a role for HNMT in histamine inactivation. Next, we performed comprehensive behavioural testing and determined that KO mice exhibited high aggressive behaviours in the resident-intruder and aggressive biting behaviour tests. High aggression in KO mice was suppressed by treatment with zolantidine, a histamine H2 receptor (H2R) antagonist, indicating that abnormal H2R activation promoted aggression in KO mice. A sleep analysis revealed that KO mice exhibited prolonged bouts of awakening during the light (inactive) period and compensatory sleep during the dark (active) period. Abnormal sleep behaviour was suppressed by treatment with pyrilamine, a H1R antagonist, prior to light period, suggesting that excessive H1R activation led to the dysregulation of sleep-wake cycles in KO mice. These observations inform the physiological roles of HNMT.