Miller Stephanie M, Kalanjati Viskasari P, Colditz Paul B, Björkman Stella Tracey
Perinatal Research Centre, UQ Centre for Clinical Research, The University of Queensland, Herston, QLD, Australia.
Dev Neurosci. 2017;39(5):375-385. doi: 10.1159/000468926. Epub 2017 May 5.
GABA is a major neurotransmitter in the mammalian brain. In the mature brain GABA exerts inhibitory actions via the GABAA receptor (GABAAR); however, in the immature brain GABA provides much of the excitatory drive. We examined the expression of 3 predominant GABAA α-subunit proteins in the pig brain at various pre- and postnatal ages. Brain tissue was collected from piglets born via caesarean section at preterm ages 91, 97, 100, and 104 days' gestational age (GA), at term equivalent (114 days' GA, caesarean section) and at term, postnatal day 0 (P0) (spontaneous delivery, term = 115 days). Tissue was obtained from piglets at P4 and P7. Adult tissue from sows was collected postmortem after caesarean section. In all cortical regions and basal ganglia (1) α3 exhibited a significant increase in protein expression at 100 days' GA, (2) α3 expression decreased with age after 100 days' GA, (3) α1 increased with age, with peak expression at P7 in cortices, hippocampus, and thalamus, and (4) α2 protein expression remained relatively constant across the ages examined. The subunit expression of α3 was most abundant at preterm ages, with α1 the predominant subunit expressed postnatally. Immunofluorescent labelling revealed α1 expression on the somatic membranes of pyramidal cells in the cortex and hippocampus, and in the cerebellar Purkinje cells. Positive α3 labelling was apparent on interneurones in the cortex and hippocampus. The switch between dominant α-subunits may coincide with the functional change in GABAergic neurotransmission from excitation to inhibition. Brain growth in the pig closely reflects that in the term human, making the pig a valuable non-primate model for studying development and the effects of insults on the perinatal brain.
γ-氨基丁酸(GABA)是哺乳动物大脑中的一种主要神经递质。在成熟大脑中,GABA通过GABAA受体(GABAAR)发挥抑制作用;然而,在未成熟大脑中,GABA提供了大部分兴奋性驱动。我们研究了猪大脑在不同产前和产后年龄时3种主要GABAAα亚基蛋白的表达情况。脑组织取自通过剖腹产出生的仔猪,这些仔猪的胎龄分别为91、97、100和104天(妊娠龄,GA),足月等效胎龄(114天GA,剖腹产)以及足月出生后第0天(P0)(自然分娩,足月=115天)。还从P4和P7的仔猪获取了组织。母猪的成年组织在剖腹产死后采集。在所有皮质区域和基底神经节中,(1)α3在100天GA时蛋白表达显著增加,(2)100天GA后α3表达随年龄下降,(3)α1随年龄增加,在皮质、海马体和丘脑的P7时表达达到峰值,(4)α2蛋白表达在所有检测年龄中保持相对恒定。α3亚基表达在早产年龄时最为丰富,α1是出生后表达的主要亚基。免疫荧光标记显示α1在皮质和海马体的锥体细胞体膜以及小脑浦肯野细胞中表达。皮质和海马体中间神经元上有明显的α3阳性标记。主要α亚基之间的转换可能与GABA能神经传递从兴奋到抑制的功能变化相吻合。猪的大脑生长与足月出生的人类大脑生长密切相似,这使得猪成为研究围产期大脑发育和损伤影响的有价值的非灵长类动物模型。