# Mechanisms of neurodevelopmental effects of parental exposure to commonly used general anesthetic agents

> **NIH NIH R56** · UNIVERSITY OF FLORIDA · 2020 · $381,250

## Abstract

Abstract
Mechanisms of neurodevelopmental effects of parental exposure to commonly used general anesthetic agents
Epidemiological studies and research in animal models demonstrate that parental germ cells are susceptible to
reprogramming by environmental factors across the lifespan. General anesthetics (GAs) can be considered as
highly active environmental factors. In our background study, we received the first experimental evidence that
a frequently used GA, sevoflurane (SEVO), administered to young adult rats, induces 1) epigenetic
reprogramming of the neuron-specific K+-2Cl- (Kcc2) Cl- exporter gene in germ cells of both exposed parents
and in the hypothalamus and hippocampus of their male, but not female, offspring; 2) the hypothalamic and
hippocampal Kcc2 expression impairment and behavioral deficiencies in these male offspring; and 3) long-term
neurobehavioral abnormalities in exposed males (but not females). The plausibility of the epigenetic germ cell
effects and, hence, intergenerational neurocognitive effects of GAs in humans is supported by findings of a
recent clinical study that the DNA methylation status of 1,509 genes in the spermatozoa of male patients was
persistently changed 1 week after bariatric surgery. The large number of young adults who require general
anesthesia and a growing number of neurodevelopmental disorders of unknown etiology in unexposed children
underscore the importance of investigating intergenerational effects of GAs. Based on our findings and extant
literature and using a neuron-specific Kcc2 as a molecular biomarker, we developed the following hypotheses,
which will be tested in three specific aims: 1: Determine whether the intergenerational effects of young adult
anesthetic exposure are specific to SEVO or occur with other GABAergic anesthetics as well. Hypotheses:
Propofol, an intravenous GA with a selective GABAAR-mediated action, but not ketamine, an intravenous GA
that blocks the NMDA receptor/channel, will induce intergenerational effects qualitatively similar to those
induced by SEVO. 2: Determine whether offspring are more susceptible to SEVO-induced neurobehavioral
abnormalities than the exposed parents. Hypotheses: Parental germ cells and brain development in their
offspring can be affected at levels/durations of SEVO exposures that are not sufficient to induce
neurobehavioral abnormalities in parents. 3: Determine whether pretreatments with dexmedetomidine or
formestane ameliorate the intergenerational effects of SEVO. Hypotheses: Formestane will alleviate SEVO-
induced neurobehavioral abnormalities in both generations, while dexmedetomidine will alleviate
neurobehavioral abnormalities in exposed parents only. The results of the proposed experiments, whose
plausibility is supported by animal and human studies, will help to identify therapeutic strategies to improve
general anesthesia safety in exposed parents and their future unexposed offspring and to form the foundation
for clinical studies of ...

## Key facts

- **NIH application ID:** 10240408
- **Project number:** 1R56HD102898-01
- **Recipient organization:** UNIVERSITY OF FLORIDA
- **Principal Investigator:** ANATOLY E MARTYNYUK
- **Activity code:** R56 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2020
- **Award amount:** $381,250
- **Award type:** 1
- **Project period:** 2020-09-01 → 2022-08-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10240408

## Citation

> US National Institutes of Health, RePORTER application 10240408, Mechanisms of neurodevelopmental effects of parental exposure to commonly used general anesthetic agents (1R56HD102898-01). Retrieved via AI Analytics 2026-05-25 from https://api.ai-analytics.org/grant/nih/10240408. Licensed CC0.

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