Murgatroyd Christopher A, Hicks-Nelson Alexandria, Fink Alexandria, Beamer Gillian, Gurel Kursat, Elnady Fawzy, Pittet Florent, Nephew Benjamin C
Manchester Metropolitan University, Centre for Healthcare Science Research , Manchester , UK.
Department of Biomedical Sciences, Cummings School of Veterinary Medicine, Tufts University , North Grafton, MA , USA.
Front Endocrinol (Lausanne). 2016 Dec 14;7:155. doi: 10.3389/fendo.2016.00155. eCollection 2016.
Recent studies support the hypothesis that the adverse effects of early-life adversity and transgenerational stress on neural plasticity and behavior are mediated by inflammation. The objective of the present study was to investigate the immune and behavioral programing effects of intranasal (IN) vasopressin (AVP) and oxytocin (OXT) treatment of chronic social stress (CSS)-exposed F1 dams on F2 juvenile female offspring. It was hypothesized that maternal AVP and OXT treatment would have preventative effects on social stress-induced deficits in offspring anxiety and social behavior and that these effects would be associated with changes in interferon-γ (IFNγ). Control and CSS-exposed F1 dams were administered IN saline, AVP, or OXT during lactation and the F2 juvenile female offspring were assessed for basal plasma IFNγ and perseverative, anxiety, and social behavior. CSS F2 female juvenile offspring had elevated IFNγ levels and exhibited increased repetitive/perseverative and anxiety behaviors and deficits in social behavior. These effects were modulated by AVP and OXT in a context- and behavior-dependent manner, with OXT exhibiting preventative effects on repetitive and anxiety behaviors and AVP possessing preventative effects on social behavior deficits and anxiety. Basal IFNγ levels were elevated in the F2 offspring of OXT-treated F1 dams, but IFNγ was not correlated with the behavioral effects. These results support the hypothesis that maternal AVP and OXT treatment have context- and behavior-specific effects on peripheral IFNγ levels and perseverative, anxiety, and social behaviors in the female offspring of early-life social stress-exposed dams. Both maternal AVP and OXT are effective at preventing social stress-induced increases in self-directed measures of anxiety, and AVP is particularly effective at preventing impairments in overall social contact. OXT is specifically effective at preventing repetitive/perseverative behaviors, yet is ineffective at preventing deficits in overall social behavior.
近期研究支持这样一种假说,即生命早期逆境和跨代应激对神经可塑性及行为的不利影响是由炎症介导的。本研究的目的是调查鼻内(IN)注射加压素(AVP)和催产素(OXT)对遭受慢性社会应激(CSS)的F1代母鼠进行治疗后,对F2代幼年雌性后代的免疫和行为编程作用。据推测,母体给予AVP和OXT治疗将对社会应激诱导的后代焦虑和社会行为缺陷具有预防作用,且这些作用将与干扰素-γ(IFNγ)的变化相关。在哺乳期,对对照母鼠和遭受CSS的F1代母鼠给予鼻内注射生理盐水、AVP或OXT,并对F2代幼年雌性后代的基础血浆IFNγ以及持续性、焦虑和社会行为进行评估。CSS组的F2代雌性幼年后代IFNγ水平升高,表现出重复/持续性行为增加、焦虑行为增加以及社会行为缺陷。这些作用受到AVP和OXT以情境和行为依赖的方式调节,其中OXT对重复和焦虑行为具有预防作用,而AVP对社会行为缺陷和焦虑具有预防作用。经OXT治疗的F1代母鼠所产F2代后代的基础IFNγ水平升高,但IFNγ与行为效应不相关。这些结果支持这样的假说,即母体给予AVP和OXT治疗对早期遭受社会应激的母鼠所产雌性后代的外周IFNγ水平以及持续性、焦虑和社会行为具有情境和行为特异性作用。母体给予AVP和OXT均可有效预防社会应激诱导的自我导向焦虑测量指标增加,且AVP在预防整体社会接触受损方面尤为有效。OXT在预防重复/持续性行为方面具有特异性效果,但在预防整体社会行为缺陷方面无效。