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PRODID:-//Vrije Universiteit Amsterdam//NONSGML v1.0//EN
NAME:PhD defence S.E. Evangelista
METHOD:PUBLISH
BEGIN:VEVENT
DTSTART:20260115T134500
DTEND:20260115T151500
DTSTAMP:20260115T134500
UID:phd-defence-s-e-evangelista@8F96275E-9F55-4B3F-A143-836282E12573
CREATED:20260825T165822
LOCATION:VU Main Building, 1105, De Boelelaan, 1081 HV, Amsterdam
SUMMARY:PhD defence S.E. Evangelista
X-ALT-DESC;FMTTYPE=text/html: <html> <body> <p><p>From Neurodevelopmen
 tal Models to Endocrine Disruption: Metabolomic Insights from In Vitr
 o and In Vivo Studies</p></p> <p><strong>Chemist Sara Evangelista foc
 used on how endocrine disrupting chemicals (EDCs) can affect early br
 ain development and contribute to long-term cognitive and behavioral 
 problems. Early life is a vulnerable period in which hormones, neurot
 ransmitters, and lipids govern key neurodevelopmental processes, maki
 ng these systems potential targets for chemical disruption.</strong><
 /p><p>To better understand the underlying mechanisms, Evangelista com
 bined rat studies with human cortical brain organoids (CBOs), an emer
 ging model that mimics early human brain development. The CBO researc
 h provided a metabolic and lipidomic reference framework for evaluati
 ng the extent to which this model reflects the neurodevelopmental pat
 hways relevant to toxicity testing. Parallel to this, she investigate
 d how perinatal exposure to selected EDCs alters metabolic and hormon
 al pathways in the developing rat hippocampus and whether these early
  changes are associated with later behavioral deficits. The overarchi
 ng motivation was to generate mechanistic insights that would support
  more predictive and human-relevant approaches to assessing developme
 ntal neurotoxicity.</p><p><strong>Normal Brain Development Can Be Dis
 rupted</strong><br>The research demonstrated that certain chemicals w
 e are exposed to daily—known as endocrine disruptors (EDCs)—can d
 isrupt normal brain development when exposure occurs very early in li
 fe. In rats, Evangelista found that these chemicals altered key molec
 ules in the developing brain, such as hormones, lipids, and neurotran
 smitters, all of which are necessary for healthy growth. Some of thes
 e early changes were associated with learning and memory problems lat
 er in life, demonstrating that early disruption can have lasting cons
 equences.</p><p><strong>Promising Laboratory Models</strong><br>Human
  stem cell-derived brain organoids ("mini-brains") have also been sho
 wn to develop metabolic characteristics similar to those observed in 
 early human brain development. This means they can serve as promising
  laboratory models for studying how chemicals can affect the developi
 ng brain without relying solely on animal testing. Overall, my work p
 rovides early warning signs and tools to better identify chemicals th
 at can harm brain development.</p><p>More information on the <a href=
 "https://hdl.handle.net/1871.1/45758ea0-6272-4a83-9a2a-e92ba48ef1a9" 
 data-new-window="true" target="_blank" rel="noopener noreferrer">thes
 is</a></p> </body> </html>
DESCRIPTION: From Neurodevelopmental Models to Endocrine Disruption: M
 etabolomic Insights from In Vitro and In Vivo Studies <strong>Chemist
  Sara Evangelista focused on how endocrine disrupting chemicals (EDCs
 ) can affect early brain development and contribute to long-term cogn
 itive and behavioral problems. Early life is a vulnerable period in w
 hich hormones, neurotransmitters, and lipids govern key neurodevelopm
 ental processes, making these systems potential targets for chemical 
 disruption.</strong>To better understand the underlying mechanisms, E
 vangelista combined rat studies with human cortical brain organoids (
 CBOs), an emerging model that mimics early human brain development. T
 he CBO research provided a metabolic and lipidomic reference framewor
 k for evaluating the extent to which this model reflects the neurodev
 elopmental pathways relevant to toxicity testing. Parallel to this, s
 he investigated how perinatal exposure to selected EDCs alters metabo
 lic and hormonal pathways in the developing rat hippocampus and wheth
 er these early changes are associated with later behavioral deficits.
  The overarching motivation was to generate mechanistic insights that
  would support more predictive and human-relevant approaches to asses
 sing developmental neurotoxicity.<strong>Normal Brain Development Can
  Be Disrupted</strong><br>The research demonstrated that certain chem
 icals we are exposed to daily—known as endocrine disruptors (EDCs)�
 ��can disrupt normal brain development when exposure occurs very earl
 y in life. In rats, Evangelista found that these chemicals altered ke
 y molecules in the developing brain, such as hormones, lipids, and ne
 urotransmitters, all of which are necessary for healthy growth. Some 
 of these early changes were associated with learning and memory probl
 ems later in life, demonstrating that early disruption can have lasti
 ng consequences.<strong>Promising Laboratory Models</strong><br>Human
  stem cell-derived brain organoids ("mini-brains") have also been sho
 wn to develop metabolic characteristics similar to those observed in 
 early human brain development. This means they can serve as promising
  laboratory models for studying how chemicals can affect the developi
 ng brain without relying solely on animal testing. Overall, my work p
 rovides early warning signs and tools to better identify chemicals th
 at can harm brain development.More information on the <a href="https:
 //hdl.handle.net/1871.1/45758ea0-6272-4a83-9a2a-e92ba48ef1a9" data-ne
 w-window="true" target="_blank" rel="noopener noreferrer">thesis</a>
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