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Intergenerational Stress Transmission is Associated with Brain Metabotranscriptome Remodeling and Mitochondrial Dysfunction

Sammy Alhassen, Siwei Chen, Lamees Alhassen, Alvin Phan, Mohammad Khoudari, Angele De Silva, Huda Barhoosh, Zitong Wang, Chelsea Parrocha, Emily Shapiro, Charity Henrich, Zicheng Wang, Leon Mutesa, Pierre Baldi, Geoffrey W. Abbott, Amal Alachkar
doi: https://doi.org/10.1101/2021.04.09.438868
Sammy Alhassen
1Department of Pharmaceutical Sciences, University of California-Irvine, CA 92697
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Siwei Chen
2Department of Computer Science, School of Information and Computer Sciences, University of California-Irvine, CA 92697
3Institute for Genomics and Bioinformatics, School of Information and Computer Sciences, University of California-Irvine, CA 92697
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Lamees Alhassen
1Department of Pharmaceutical Sciences, University of California-Irvine, CA 92697
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Alvin Phan
1Department of Pharmaceutical Sciences, University of California-Irvine, CA 92697
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Mohammad Khoudari
1Department of Pharmaceutical Sciences, University of California-Irvine, CA 92697
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Angele De Silva
4Bioelectricity Laboratory, Department of Physiology and Biophysics, School of Medicine, University of California-Irvine, CA 92697
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Huda Barhoosh
1Department of Pharmaceutical Sciences, University of California-Irvine, CA 92697
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Zitong Wang
1Department of Pharmaceutical Sciences, University of California-Irvine, CA 92697
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Chelsea Parrocha
1Department of Pharmaceutical Sciences, University of California-Irvine, CA 92697
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Emily Shapiro
1Department of Pharmaceutical Sciences, University of California-Irvine, CA 92697
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Charity Henrich
1Department of Pharmaceutical Sciences, University of California-Irvine, CA 92697
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Zicheng Wang
1Department of Pharmaceutical Sciences, University of California-Irvine, CA 92697
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Leon Mutesa
5Center for Human Genetics, College of Medicine and Health Sciences, University of Rwanda, Kigali
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Pierre Baldi
2Department of Computer Science, School of Information and Computer Sciences, University of California-Irvine, CA 92697
3Institute for Genomics and Bioinformatics, School of Information and Computer Sciences, University of California-Irvine, CA 92697
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Geoffrey W. Abbott
4Bioelectricity Laboratory, Department of Physiology and Biophysics, School of Medicine, University of California-Irvine, CA 92697
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Amal Alachkar
1Department of Pharmaceutical Sciences, University of California-Irvine, CA 92697
3Institute for Genomics and Bioinformatics, School of Information and Computer Sciences, University of California-Irvine, CA 92697
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  • For correspondence: aalachka@uci.edu
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Abstract

Intergenerational stress increases lifetime susceptibility to depression and other psychiatric disorders. Whether intergenerational stress transmission is a consequence of in utero neurodevelopmental disruptions vs early-life mother-infant interaction is largely unknown. Here, we demonstrated that exposure to traumatic stress in mice during pregnancy, through predator scent exposure, induces in the offspring social deficits and depressive-like behavior. We found, through cross-fostering experiments, that raising of normal pups by traumatized mothers produced a similar behavioral phenotype to that induced in pups raised by their biological traumatized mothers. Good caregiving (by non-traumatized mothers), however, did not completely protect against the prenatal trauma-induced behavioral deficits. These findings support a two-hit stress mechanism of both in utero and early-life parenting (poor caregiving by the traumatized mothers) environments. Associated with the behavioral deficits, we found profound changes in brain metabolomics and transcriptomic (metabotranscriptome). Striking increases in the mitochondrial hypoxia marker and epigenetic modifier 2-hydroxyglutaric acid, in the brains of neonatal and adult pups whose mothers were exposed to stress during pregnancy, indicated mitochondrial metabolism dysfunctions and epigenetic mechanisms. Bioinformatic analyses revealed mechanisms involving stress- and hypoxia-response metabolic pathways in the brains of the neonatal mice, which appear to lead to long-lasting alterations in mitochondrial-energy metabolism, and epigenetic processes pertaining to DNA and chromatin modifications. Most strikingly, we demonstrated that an early pharmacological intervention that can correct mitochondria metabolism - lipid metabolism and epigenetic modifications with acetyl-L-carnitine (ALCAR) supplementation - produces long-lasting protection against the behavioral deficits associated with intergenerational transmission of traumatic stress.

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Competing Interest Statement

The authors have declared no competing interest.

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The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted April 10, 2021.
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Intergenerational Stress Transmission is Associated with Brain Metabotranscriptome Remodeling and Mitochondrial Dysfunction
Sammy Alhassen, Siwei Chen, Lamees Alhassen, Alvin Phan, Mohammad Khoudari, Angele De Silva, Huda Barhoosh, Zitong Wang, Chelsea Parrocha, Emily Shapiro, Charity Henrich, Zicheng Wang, Leon Mutesa, Pierre Baldi, Geoffrey W. Abbott, Amal Alachkar
bioRxiv 2021.04.09.438868; doi: https://doi.org/10.1101/2021.04.09.438868
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Intergenerational Stress Transmission is Associated with Brain Metabotranscriptome Remodeling and Mitochondrial Dysfunction
Sammy Alhassen, Siwei Chen, Lamees Alhassen, Alvin Phan, Mohammad Khoudari, Angele De Silva, Huda Barhoosh, Zitong Wang, Chelsea Parrocha, Emily Shapiro, Charity Henrich, Zicheng Wang, Leon Mutesa, Pierre Baldi, Geoffrey W. Abbott, Amal Alachkar
bioRxiv 2021.04.09.438868; doi: https://doi.org/10.1101/2021.04.09.438868

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