Audero Enrica, Coppi Elisabetta, Mlinar Boris, Rossetti Tiziana, Caprioli Antonio, Banchaabouchi Mumna Al, Corradetti Renato, Gross Cornelius
Mouse Biology Unit, European Molecular Biology Laboratory (EMBL), Via Ramarini 32, 00015 Monterotondo, Italy.
Science. 2008 Jul 4;321(5885):130-3. doi: 10.1126/science.1157871.
Sudden infant death syndrome is the leading cause of death in the postneonatal period in developed countries. Postmortem studies show alterations in serotonin neurons in the brainstem of such infants. However, the mechanism by which altered serotonin homeostasis might cause sudden death is unknown. We investigated the consequences of altering the autoinhibitory capacity of serotonin neurons with the reversible overexpression of serotonin 1A autoreceptors in transgenic mice. Overexpressing mice exhibited sporadic bradycardia and hypothermia that occurred during a limited developmental period and frequently progressed to death. Moreover, overexpressing mice failed to activate autonomic target organs in response to environmental challenges. These findings show that excessive serotonin autoinhibition is a risk factor for catastrophic autonomic dysregulation and provide a mechanism for a role of altered serotonin homeostasis in sudden infant death syndrome.
婴儿猝死综合征是发达国家新生儿后期死亡的主要原因。尸检研究表明,此类婴儿脑干中的血清素神经元存在改变。然而,血清素稳态改变可能导致猝死的机制尚不清楚。我们通过在转基因小鼠中可逆性过表达血清素1A自身受体,研究了改变血清素神经元自身抑制能力的后果。过表达小鼠在有限的发育阶段出现散发性心动过缓和体温过低,并经常发展至死亡。此外,过表达小鼠在面对环境挑战时无法激活自主目标器官。这些发现表明,血清素过度自身抑制是灾难性自主神经调节异常的一个风险因素,并为血清素稳态改变在婴儿猝死综合征中的作用提供了一种机制。