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Discerning Comparison of 1 and 0.5% Ethylene Glycol in Sprague-Dawley Rats with Modeled Urolithiasis
A V Bervinova1,2, N A Borozdina3,4, V A Palikov1
1Branch of M. M. Shemyakin and Yu. A. Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, Pushchino, Russia.
Bulletin of Experimental Biology and Medicine
|October 9, 2022
Summary
A new rat model for urolithiasis uses a low-dose ethylene glycol (0.5%) for six weeks, showing disease development without severe organ toxicity. This long-term model allows for a six-week recovery observation period.
Area of Science:
- Nephrology
- Toxicology
- Animal Modeling
Background:
- Ethylene glycol is commonly used to model urolithiasis in rats.
- High concentrations (1-0.75%) can cause rapid disease progression and multi-organ toxicity.
- Ethical concerns limit the duration of experiments with high-dose ethylene glycol.
Purpose of the Study:
- To develop a safer, long-term rat model for studying urolithiasis.
- To assess the feasibility of using a lower concentration of ethylene glycol for chronic urolithiasis induction.
- To evaluate the absence of organ toxicity in this modified model.
Main Methods:
- Sprague-Dawley rats were administered a low concentration (0.5%) of ethylene glycol for six weeks.
- Animals were observed during a subsequent six-week recovery period.
- Urine and blood parameters were analyzed to monitor urolithiasis development and organ function.
Main Results:
- Urolithiasis signs, including ketones, decreased diuresis, and lower urine pH, appeared by week six.
- Elevated blood urea, protein, and hematocrit were observed.
- No leukocytes in urine, normal differential leukocyte count, and no elevation in ALT, creatinine, cholesterol, or triglycerides indicated an absence of organ failure.
- The 0.5% ethylene glycol model allowed for observation up to 12 weeks, unlike the 1% model stopped at week three due to ethical concerns.
Conclusions:
- A 0.5% ethylene glycol concentration in rats provides a viable long-term model for urolithiasis.
- This model effectively induces urolithiasis without causing significant multi-organ toxicity.
- The extended observation period in this modified model offers greater insight into disease progression and recovery.

