Manoni Greta, Puzzo Concetto, Gigantesco Antonella, Adriani Walter
Faculty of Psychology, Università Telematica Internazionale Uninettuno, 00100 Rome, Italy.
Istituto Superiore di Sanità, Center of Behavioural Science and Mental Health, 00100 Rome, Italy.
Brain Sci. 2022 Mar 31;12(4):469. doi: 10.3390/brainsci12040469.
Dopamine transporter (DAT) is involved in dopamine (DA) reuptake in presynaptic terminals. Deletion of DAT results in a hyperdopaminergic KO-rat phenotype. To conduct our studies in heterozygous DAT rats, several pedigree lines were created, with known derivation of the allele (i.e., maternal or paternal). Our purpose was to elucidate the role of parental origin rather than maternal care, assessing if maternal maltreatments generated sequelae in female offspring. In the first experiment, female rats and their pups were observed during postnatal lactation. Control dams were WT and heterozygous ones were MAT (but K-MAT, with previous experience of early maltreatment by their KO adoptive dams). WT dams were highly attracted to their offspring (predictably, they spent a lot of time licking their pups); in contrast, K-MAT dams showed strangely comparable levels of caring for their pups and exploring the environment. Subsequently, peculiar features of the circadian cycle were found in adolescent rats with different epigenotypes (WT, MUX = offspring of MAT father, MIK = offspring of K-MAT dam). The MIK epigenotype produced locomotor hyperactivity also during resting hours, well above typical values. The MUX epigenotype, on the other hand, was less active and presented a depression-like profile. This study is unique: maltreatment was generated in a spontaneous way from a DAT-KO mother to offspring. We highlight how future studies will address separate contributions by genotype and upbringing. In conclusion, paternal-allele asset generates sequelae diametrically opposed to the inheritance of early maternal trauma.
多巴胺转运体(DAT)参与突触前终末的多巴胺(DA)重摄取。DAT缺失会导致多巴胺能亢进的基因敲除大鼠表型。为了在杂合子DAT大鼠中开展我们的研究,我们创建了几个谱系品系,其等位基因的来源是已知的(即母系或父系)。我们的目的是阐明亲本来源而非母性照料的作用,评估母体虐待是否会在雌性后代中产生后遗症。在第一个实验中,在产后哺乳期观察雌性大鼠及其幼崽。对照母鼠为野生型(WT),杂合子母鼠为MAT(但K-MAT,其曾有过被基因敲除的代孕母鼠早期虐待的经历)。野生型母鼠对其后代极具吸引力(不出所料,它们花大量时间舔舐幼崽);相比之下,K-MAT母鼠在照料幼崽和探索环境方面表现出奇怪的同等水平。随后,在具有不同表观基因型的青春期大鼠(WT、MUX = MAT父本的后代、MIK = K-MAT母本的后代)中发现了昼夜节律周期的特殊特征。MIK表观基因型在休息时间也会产生运动活动亢进,远高于典型值。另一方面,MUX表观基因型活动较少,呈现出类似抑郁的特征。这项研究很独特:虐待是由基因敲除的DAT母鼠自发传递给后代的。我们强调未来的研究将如何探讨基因型和养育方式的单独作用。总之,父系等位基因资产产生的后遗症与早期母体创伤的遗传后果截然相反。