Long-lasting behavioral and neurochemical effects of early-life environmental enrichment in rats submitted to neonatal morphine administration

被引:1
|
作者
Nascimento, Matheus Gabriel de Freitas [1 ,2 ]
de Castro, Josimar Macedo [2 ,3 ]
Medeiros, Liciane Fernandes [2 ,4 ]
Fiuza, Khetruein Jordana [2 ]
de Oliveira, Thais Collioni [2 ]
Morais, Iala Thais de Sousa [1 ,2 ]
Dal Bosco, Tenille [2 ,3 ]
Caumo, Wolnei [2 ]
Stein, Dirson J. [2 ,3 ]
Torres, Iraci L. S. [1 ,2 ,3 ]
机构
[1] Univ Fed Rio Grande do Sul UFRGS, Inst Basic Hlth Sci ICBS, Postgrad Program Biol Sci Pharmacol & Therapeut, Porto Alegre, RS, Brazil
[2] Hosp Clin Porto Alegre HCPA, Pharmacol Pain & Neuromodulat Lab, Preclin Invest, Porto Alegre, RS, Brazil
[3] Univ Fed Rio Grande do Sul, Med Sch, Postgrad Program Med Med Sci, Porto Alegre, Brazil
[4] Univ La Salle, Postgrad Program Hlth & Human Dev, Canoas, RS, Brazil
关键词
environmental enrichment; hyperalgesia; morphine; neonatal rats; ELEVATED PLUS-MAZE; NEUROTROPHIC FACTOR; INDUCED ANTINOCICEPTION; TERM-MEMORY; SPINAL-CORD; BDNF LEVELS; STIMULATION; EXPOSURE; INCREASES; ANXIETY;
D O I
10.1002/jdn.10378
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The present study examined the medium- and long-term effects of early environmental enrichment (EE) on neuromotor, nociceptive, cognitive, behavioral, and neurochemical parameters in newborn rats repeatedly exposed to morphine. The study employed 90 Wistar rats: 10 adult nulliparous females and 80 male pups. Litter was split into standard and EE housing. Following, half of each litter received saline (S) or morphine (M) injections, resulting in four groups: SC + S, EE + S, SC + M, and EE + M. EE was applied from PND1 to PND21, while morphine or saline was given daily (5 mu g/s.c.) from PND8 to PND14. Neuromotor development was similar between groups. In the OF test, morphine reduced outer and total crossings, whereas EE increased inner crossings and rearings. Adult rats showed a decrease in outer and total crossings and grooming and an increase in rearing. EE increased the number of protected and unprotected head dipping. Adult rats showed an increase in protected head dipping. Adult rats showed a lower recognition index, and, when exposed to EE, a lower anxiety index and analgesia. EE increased brainstem and hippocampal BDNF levels. Adult rats had increased hypothalamus, spinal cord, and brainstem BDNF levels, an increase in the spinal cord, and decreased hypothalamus TNF-alpha levels. This study demonstrated that early-life EE raises BDNF levels in the brainstem and hippocampus of rats and modifies their behaviors (such as nociception, exploration, and anxiety) in a state-dependent manner (morphine and age). The primary medium- and long-term effects of EE alone (label A), and in a state-dependent manner (age and/or morphine; label B) on behavioral events inopen field (OF), elevated plus-maze (EPM), and hot plate (HP) tests, alongside neurochemical parameters (TNF-alpha, tumor necrosis factor-alpha; BDNF, brain-derived neurotrophic factor), in brainstem and hippocampus. The arrows indicate the direction of the EE effect on a given variable; those pointing upwards indicate an increase, while those pointing downwards indicate a reduction. image
引用
收藏
页码:877 / 893
页数:17
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