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MacDowell Kaswan, Z.

Publications and source records attributed to MacDowell Kaswan, Z..

3 recordsLinked to original sources

Erratic Maternal Care Induces Avoidant-Like Attachment Deficits in a Mouse Model of Early Life Adversity

Attachment theory offers an important clinical framework for understanding and treating negative effects of early life adversity. Attachment styles emerge during critical periods of development in response to caregivers ability to consistently meet their offsprings needs. Attachment styles are classified as secure or insecure (anxious, avoidant, or disorganized), with rates of insecure attachment rising in high-risk populations and correlating with a plethora of negative health outcomes throughout life. Despite its importance, little is known about the neural basis of attachment. Work in rats has demonstrated that limited bedding and nesting (LB) impairs maternal care and produces abnormal maternal attachment linked to increased pup corticosterone. However, the effects of LB on attachment-like behavior have not been investigated in mice where additional genetic and molecular tools are available. Furthermore, no group has utilized home-cage monitoring to link abnormal maternal care with deficits in attachment-like behavior. Using home-cage monitoring, we confirmed a robust increase in maternal fragmentation among LB dams. Abnormal maternal care was correlated with elevated corticosterone levels on post-natal day seven (P7) and a stunted growth trajectory that persisted later in life. LB did not alter maternal buffering at P8 or maternal preference at P18, indicating that certain attachment-like behaviors remain unaffected despite exposure to high levels of erratic maternal care. However, LB pups vocalized less in response to maternal separation at P8, did not readily approach their dam at P13, and exhibited higher anxiety-like behavior at P18, suggesting that LB induces avoidant-like attachment deficits in mice. Significance StatementThe impoverished conditions of limited bedding and nesting (LB) cause erratic maternal care and elevated corticosterone levels in rat and mouse pups. The increase in corticosterone levels causes attachment-like deficits in rat pups; however, it remains unclear whether similar deficits are observed in mice, where additional genomic and molecular tools are available. Using continuous home-cage monitoring, we confirmed a substantial increase in erratic maternal care and elevated corticosterone levels in 7-day-old mouse pups. LB mouse pups exhibited attachment-like deficits in some, but not all, tests, underscoring the robustness of this evolutionarily conserved bond. Despite some similarities, the attachment abnormalities observed in mice differed from previous reports in rats, paving the way for in-depth mechanistic studies in mice.

neuroscience↗

Postnatal Enrichment Corrects Deficits in Perineuronal Net Formation and Reversal Learning in Adult Mice Exposed to Early Adversity

Withdrawal StatementThe authors have withdrawn this manuscript because the behavioral studies using the Barnes maze were not conducted according to the methods described, specifically regarding the animals ability to locate the escape hole independently. Furthermore, the authors were unable to replicate the behavioral outcomes originally reported when the experiments were repeated following the stated methods. Therefore, the authors do not wish this work to be cited as reference for the project. If you have any questions, please contact the corresponding author.

neuroscience↗

Transient Impairment in Microglial Function Causes Sex-Specific Deficits in Synaptic and Hippocampal Function in Mice Exposed to Early Adversity

Abnormal development and function of the hippocampus are two of the most consistent findings in humans and rodents exposed to early life adversity, with males often being more affected than females. Using the limited bedding (LB) paradigm as a rodent model of early life adversity, we found that male adolescent mice that had been exposed to LB exhibit significant deficits in contextual fear conditioning and synaptic connectivity in the hippocampus, which are not observed in females. This is linked to altered developmental refinement of connectivity, with LB severely impairing microglial-mediated synaptic pruning in the hippocampus of male and female pups on postnatal day 17 (P17), but not in adolescent P33 mice when levels of synaptic engulfment by microglia are substantially lower. Since the hippocampus undergoes intense synaptic pruning during the second and third weeks of life, we investigated whether microglia are required for the synaptic and behavioral aberrations observed in adolescent LB mice. Indeed, transient ablation of microglia from P13-21, in normally developing mice caused sex-specific behavioral and synaptic abnormalities similar to those observed in adolescent LB mice. Furthermore, chemogenetic activation of microglia during the same period reversed the microglial-mediated phagocytic deficits at P17 and restored normal contextual fear conditioning and synaptic connectivity in adolescent LB male mice. Our data support an additional contribution of astrocytes in the sex-specific effects of LB, with increased expression of the membrane receptor MEGF10 and enhanced synaptic engulfment in hippocampal astrocytes of 17-day-old LB females, but not in LB male littermates. This finding suggests a potential compensatory mechanism that may explain the relative resilience of LB females. Collectively, these studies highlight a novel role for glial cells in mediating sex-specific hippocampal deficits in a mouse model of early-life adversity.

neuroscience↗