Back

A neonatal rat sepsis score captures the time course and severity of disease in a clinically relevant rat peritonitis model.

Jahandideh, F.; Liu, S. N.; Tworek, K.; Noble, R.; Rachid, J.-J. R.; MacLellan, A.; Lalu, M.; Macala, K. F.; Bourque, S. L.

2026-05-19 physiology
10.64898/2026.05.15.725467 bioRxiv
Show abstract

BackgroundNeonatal sepsis is a major cause of infant morbidity and mortality worldwide, particularly in preterm and very low birthweight babies. Fundamental differences between neonates and adults warrant clinically relevant models of neonatal sepsis. Here, we describe a preclinical fecal-slurry (FS)-induced peritonitis model of polymicrobial sepsis in neonatal rats, along with a novel neonatal rat sepsis score (nRSS) to monitor illness severity. MethodsPeritonitis was induced in 3-day-old Sprague Dawley rats by intraperitoneal injection of various doses (0.3-1.5mg/g body weight) of fecal slurry (FS); control pups received equivalent doses of vehicle. All pups received analgesics (buprenorphine), antibiotics (ampicillin and gentamicin), and fluids (saline) to model clinical standards of sepsis treatment. Time-dependent changes in circulating cytokines (IL-6, IL-1{beta}) and biomarkers of sepsis pathology (hemoglobin, glucose, alanine transaminase [ALT] levels) were assessed and correlated with nRSS scores. ResultsFS administration caused a dose-dependent increase in severity of sepsis over time, as indicated by increases in mortality rates (based on predefined criteria for euthanasia), nRSS scores, as well as time-dependent changes in circulating glucose, hemoglobin, IL-6, IL-1{beta}, and ALT activity levels. nRSS scores correlated with all quantitative measures of sepsis pathology. Notably, females showed higher mortality and higher early NRSS scores than males at moderate to high FS doses, yet biochemical markers and time of death did not differ between sexes, suggesting that the apparent female vulnerability may reflect more conspicuous behavioral manifestations of illness rather than greater underlying physiological severity. ConclusionInduction of peritonitis in rats at postnatal day 3 produced a consistent and reproducible model of polymicrobial neonatal sepsis. Illness severity was monitored using a newly developed nRSS. By minimizing distress and incorporating standards of care, this model and scoring system may serve as a platform for future investigations into the underlying mechanisms and potential therapeutic interventions for neonatal sepsis. ImpactO_LIA clinically relevant rat model of neonatal polymicrobial sepsis was developed, incorporating standards of care (analgesics, antibiotics, and fluid resuscitation) to better reflect the clinical context in which preclinical findings must ultimately translate. C_LIO_LIA novel neonatal rat sepsis scoring system (nRSS) was developed and validated, providing a sensitive, non-invasive measure of disease severity that correlates with biochemical markers and predicts mortality. C_LIO_LIFemale pups showed higher mortality and earlier behavioral signs of illness than males despite equivalent biochemistry, highlighting that clinical scores may capture sex-dependent vulnerability not apparent in standard biochemical measures. C_LIO_LITogether, this model and scoring system offer a refined platform for mechanistic and therapeutic studies of neonatal sepsis while advancing the welfare-conscious 3Rs principles essential to rigorous preclinical research C_LI

Matching journals

The top 9 journals account for 50% of the predicted probability mass.

1
PLOS ONE
4510 papers in training set
Top 5%
23.3%
2
Frontiers in Physiology
93 papers in training set
Top 0.4%
7.0%
3
Scientific Reports
3102 papers in training set
Top 21%
5.0%
4
Biomedicines
66 papers in training set
Top 0.1%
3.7%
5
Physiological Reports
35 papers in training set
Top 0.2%
3.2%
6
American Journal of Physiology-Regulatory, Integrative and Comparative Physiology
13 papers in training set
Top 0.1%
2.8%
7
Frontiers in Medicine
113 papers in training set
Top 2%
2.4%
8
Nature Communications
4913 papers in training set
Top 50%
1.8%
9
Frontiers in Immunology
586 papers in training set
Top 4%
1.8%
50% of probability mass above
10
JCI Insight
241 papers in training set
Top 4%
1.5%
11
Disease Models & Mechanisms
119 papers in training set
Top 1%
1.5%
12
Journal of the American Heart Association
119 papers in training set
Top 3%
1.5%
13
Critical Care Explorations
15 papers in training set
Top 0.3%
1.3%
14
BMJ Open
554 papers in training set
Top 11%
1.0%
15
Brain, Behavior, and Immunity
105 papers in training set
Top 2%
0.9%
16
The FASEB Journal
175 papers in training set
Top 2%
0.9%
17
Journal of Clinical Investigation
164 papers in training set
Top 5%
0.9%
18
The Journal of Pediatrics
15 papers in training set
Top 0.5%
0.9%
19
Life Sciences
25 papers in training set
Top 1%
0.8%
20
Physiological Genomics
15 papers in training set
Top 0.3%
0.8%
21
American Journal of Physiology-Lung Cellular and Molecular Physiology
39 papers in training set
Top 0.4%
0.8%
22
Journal of Clinical Medicine
91 papers in training set
Top 6%
0.8%
23
Journal of Neurology, Neurosurgery & Psychiatry
29 papers in training set
Top 1%
0.8%
24
BMC Infectious Diseases
118 papers in training set
Top 5%
0.8%
25
PeerJ
261 papers in training set
Top 14%
0.8%
26
Cell Reports Medicine
140 papers in training set
Top 7%
0.8%
27
PLOS Biology
408 papers in training set
Top 19%
0.8%
28
Frontiers in Pediatrics
29 papers in training set
Top 0.8%
0.8%
29
Nutrients
64 papers in training set
Top 2%
0.8%
30
Critical Care
14 papers in training set
Top 0.6%
0.7%