Frank et al. (2018): Neuronal Network IVIVE"

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from "Defining toxicological tipping points in neuronal network development"

Christopher L. Frank, Jasmine P. Brown, Kathleen Wallace, John F. Wambaugh, Imran Shah, and Timothy J. Shafer

Toxicology and Applied Pharmacology 354 (2018) 81-93


Measuring electrical activity of neural networks by microelectrode array (MEA) has recently shown promise for screening level assessments of chemical toxicity on network development and function. Important aspects of interneuronal communication can be quantified from a single MEA recording, including individual firing rates, coordinated bursting, and measures of network synchrony, providing rich datasets to evaluate chemical effects. Further, multiple recordings can be made from the same network, including during the formation of these networks in vitro. The ability to perform multiple recording sessions over the in vitro development of network activity may provide further insight into developmental effects of neurotoxicants. In the current study, a recently described MEA-based screen of 86 compounds in primary rat cortical cultures over 12 days in vitro was revisited to establish a framework that integrates all available primary measures of electrical activity from MEA recordings into a composite metric for deviation from normal activity (total scalar perturbation). Examining scalar perturbations over time and increasing concentration of compound allowed for definition of critical concentrations or "tipping points" at which the neural networks switched from recovery to non-recovery trajectories for 42 compounds. These tipping point concentrations occurred at predominantly lower concentrations than those causing overt cell viability loss or disrupting individual network parameters, suggesting tipping points may be a more sensitive measure of network functional loss. Comparing tipping points for six compounds with plasma concentrations known to cause developmental neurotoxicity in vivo demonstrated strong concordance and suggests there is potential for using tipping points for chemical prioritization.

HTTK Version

This vignette was created with httk v1.8. Although we attempt to maintain backward compatibility, if you encounter issues with the latest release of httk and cannot easily address the changes, historical versions of httk are available from:

Prepare for session

R package knitr generates html and PDF documents from this RMarkdown file, Each bit of code that follows is known as a "chunk". We start by telling knitr how we want our chunks to look.

knitr::opts_chunk$set(echo = TRUE, fig.width=5, fig.height=4)

Clear the memory

It is a bad idea to let variables and other information from previous R sessions float around, so we first remove everything in the R memory.


eval = execute.vignette

If you are using the RMarkdown version of this vignette (extension, .RMD) you will be able to see that several chunks of code in this vignette have the statement "eval = execute.vignette". The next chunk of code, by default, sets execute.vignette = FALSE. This means that the code is included (and necessary) but was not run when the vignette was built. We do this because some steps require extensive computing time and the checks on CRAN limit how long we can spend building the package. If you want this vignette to work, you must run all code, either by cutting and pasting it into R. Or, if viewing the .RMD file, you can either change execute.vignette to TRUE or press "play" (the green arrow) on each chunk in RStudio.

# Set whether or not the following chunks will be executed (run):
execute.vignette <- FALSE

Load the relevant libraries

We use the command 'library()' to load various R packages for our analysis. If you get the message "Error in library(X) : there is no package called 'X'" then you will need to install that package:

From the R command prompt:


Or, if using RStudio, look for 'Install Packages' under 'Tools' tab.


Function to format scientific notation

From ```{R scientific.notation, eval = execute.vignette} scientific_10 <- function(x) {
out <- gsub("1e", "10^", scientific_format()(x))
out <- gsub("\+","",out)
out <- gsub("10\^01","10",out)
out <- parse(text=gsub("10\^00","1",out))

### Load the data
chem.table <- Frank2018invivo

Use HTTK to perform IVIVE

This loops through each study design in the table and runs solve_pbtk:

```{R ivive.loop, eval = execute.vignette} for (this.row in 1:dim(chem.table)[1]) { this.cas <- chem.table[this.row,"Substance_CASRN"] if (tolower(chem.table[this.row,"Species"])=="rodent") {
this.species <- "rat" } else if (tolower(chem.table[this.row,"Species"])=="rat") { this.species <- "rat" } else if (tolower(chem.table[this.row,"Species"])=="human") { this.species <- "human" } else if (tolower(chem.table[this.row,"Species"])=="mouse") { this.species <- "mouse" } else browser() if (chem.table[this.row,"Route"] %in% c("i.p.","s.c.","i.m.")) iv.dose =TRUE else if (chem.table[this.row,"Route"]=="oral") iv.dose = F else browser() this.dose <- chem.table[this.row,"Dose"] this.days <- chem.table[this.row,"Days"]

Make sure the dose units are in mg/kg body weight:

if (regexpr("ug",chem.table[this.row,"Dose.Units"])!=-1) { this.dose <- this.dose/1000 } if (regexpr("/kg",chem.table[this.row,"Dose.Units"])==-1) { this.dose <- this.dose/0.25 }

Here we run the HTTK PBPK Model:

out <- suppressWarnings(solve_pbtk(chem.cas=this.cas, dose=this.dose, species=this.species,

This was used in 2017 but I don't agree with it anymore:



Record the Cmax and the AUC:

chem.table[this.row,"Cmax"] <- max(out[,"Cplasma"]) chem.table[this.row,"AUC"] <- max(out[,"AUC"]) }

## Make the plot
Comparison between predicted plasma levels for critical
concentrations and in vivo estimates from the httk model. For
those chemicals with 1) in vitro predicted critical concentrations,
2) in vivo studies indicating neurological effect, and 3)
available toxicokinetic data the time-integrated plasma concentration
(area under the curve or AUC) was predicted for the
LOEL associated with each chemical-specific study. The chemical-
specific prediction is indicated by the first four letters of
each chemicals name. There were two available studies for each
chemical. The identity ("perfect predictor") line is indicated by
a solid black line, while the dashed lines indicate ten-fold above
and below perfect prediction. Because all in vitro treatments
were exposed for the same amount of time, the relationship
between nominal in vitro concentration and time-integrated
concentration is a constant.
```{R Frank2018.Fig6, eval = execute.vignette}
Fig.AUC <- ggplot(data=chem.table) +
#  geom_point(aes(x=AUC,y=Critical.concentration,color="Chemical"))+ 
   geom_text(aes(x=AUC,y=Critical.concentration,label=Compound.abbrev,color=Chemical)) +
   scale_y_log10(label=scientific_10,limits=c(10^-7,100)) +
   scale_x_log10(label=scientific_10,limits=c(10^-7,100)) +
    annotation_logticks() + 
    geom_abline(slope=1, intercept=0) + 
    geom_abline(slope=1, intercept=1,linetype="dashed") + 
    geom_abline(slope=1, intercept=-1,linetype="dashed") + 
    xlab(expression(paste(italic("In vivo")," AUC estimated with HTTK (uM*day)"))) + 
    ylab(expression(paste(italic("In vitro")," predicted Critical Conc. (uM)"))) +
    scale_color_brewer(palette="Set2") + 
    theme_bw()  +


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httk documentation built on June 22, 2024, 6:48 p.m.