Research Article | Open Access
Evon S. Ereifej, Seth M. Meade, Cara S. Smith, Keying Chen, Nanette Kleinman, Jeffrey R. Capadona, "Status Epilepticus due to Intraperitoneal Injection of Vehicle Containing Propylene Glycol in Sprague Dawley Rats", Veterinary Medicine International, vol. 2017, Article ID 1757059, 6 pages, 2017. https://doi.org/10.1155/2017/1757059
Status Epilepticus due to Intraperitoneal Injection of Vehicle Containing Propylene Glycol in Sprague Dawley Rats
Published reports of status epilepticus due to intraperitoneal injection containing propylene glycol in rats are sparse. In fact, there are no reports specifying a maximum safe dose of propylene glycol through intraperitoneal administration. We report here a case of unexpected seizures in Sprague Dawley rats after receiving an intraperitoneal injection containing propylene glycol. Nine-week-old, 225–250 gram male rats were reported to experience tremor progressing to seizures within minutes after given injections of resveratrol (30 mg/kg) dissolved in a 40 : 60 propylene glycol/corn oil vehicle solution by direct intraperitoneal (IP) slow bolus injection or via a preplaced intraperitoneal catheter. The World Health Organization suggests a maximum dose of 25 mg/kg/day of propylene glycol taken orally and no more than 25 mg/dL in blood serum, whereas the animals used in our study got a calculated maximum 0.52 g/kg (25 times lower dose). Blood tests from the seizing rat support a diagnosis of hemolysis and lactic acidosis which may have led to the seizures, all of which appeared to be a consequence of the propylene glycol administration. These findings are consistent with oral and intravenous administration of propylene glycol toxicity as previously reported in other species, including humans. To our knowledge, this report represents the first published case of status epilepticus due to an IP injection containing propylene glycol.
Propylene glycol is a clear, colorless, odorless compound commonly used in pharmaceuticals, cosmetics, and food [1, 2]. Several studies have shown propylene glycol is safe and not toxic [2–6]. Specifically studying rats, Gaunt et al. performed toxicological studies by feeding Charles River CD strain Sprague Dawley rats with diets containing 0–50,000 ppm (equivalent to 2–5 g/kg/day) propylene glycol for two years. They observed no differences in mortality, body-weight gain, food consumption, hematology, urinary cell excretion, or any other pathological findings between controls and groups fed with propylene glycol in their diets . Years later in 1982, the Food and Drug Administration classified propylene glycol as “generally regarded as safe” . Furthermore, the World Health Organization suggests a maximum dose of 25 mg/kg/day of propylene glycol taken orally and no more than 25 mg/dL in blood serum [1, 7, 8]. To date, there is no information on the bioavailability or toxicity of propylene glycol delivered intraperitoneally.
This report discusses a case in which propylene glycol was used to dissolve resveratrol for IP slow bolus administration to rats. Propylene glycol has been used to dissolve resveratrol in several studies, some of which safely used up to 50% propylene glycol in a rodent model [9, 10]. The majority of published warnings against the use of propylene glycol as a vehicle for insoluble drugs are for epileptic studies and human patients [11–13]. Studies have shown propylene glycol can influence seizures in animal models of epilepsy and warn against using propylene glycol as the solvent to dissolve epileptic drugs such as carbamazepine, trimethadione, and benzodiazepines [2, 3, 11, 13]. Recent clinical data has shown toxicity of propylene glycol secondary to lactic acidosis, resulting from the metabolism of propylene glycol, after intravenous administration of an antibiotic medication, trimethoprim-sulfamethoxazole, which contains propylene glycol . We report here a case of unexpected seizures in Sprague Dawley rats after receiving an intraperitoneal injection of resveratrol in a 40 : 60 propylene glycol/corn oil vehicle solution.
2. Case Presentation
Nine-week-old, 225–250 gram male rats were reported to experience tremor progressing to seizures within minutes after given slow bolus intraperitoneal (IP) injections of sterile resveratrol (30 mg/kg; Mega Resveratrol, Candlewood Stars Inc.) dissolved in 40 : 60 propylene glycol/corn oil (Sigma Aldrich) vehicle solution (equivalent to 0.52 g/kg of propylene glycol). The Sprague Dawley rats were part of an IACUC approved protocol. The rats were housed at the Louis Stokes Cleveland Veteran Affairs Medical Center in AAALAC-accredited animal research facilities. Upon arrival, rats were housed in a temperature (21 ± 2°C) and humidity (30% to 70%) controlled room with a 12 : 12 hr light : dark cycle. Standard rodent chow (Teklad irradiated 7912 rat diet, Harlan Teklad, Madison, WI) and autoclaved reverse-osmosis–purified water supplied by water bottle were freely available. Sprague Dawley rats were monitored quarterly by sentinels housed in the same room which were documented to be free of viruses (Charles River Research Animal Diagnostic Services Rat Tracking Profile), mites, pinworms (PCR), and enteric protozoa and helicobacter spp. (PCR).
The Sprague Dawley rats reported on in this manuscript are a part of an ongoing drug study evaluating the use of resveratrol to reduce neurodegeneration and improve intracortical microelectrode recording quality. At the time of incidence, there were another five animals ongoing with the study receiving resveratrol every other day for up to 7 weeks without any complications. All animals underwent craniotomies in which Michigan style intracortical microelectrodes (NeuroNexus, Ann Arbor, Michigan) were implanted into the primary motor cortex. Animals received a preoperative injection of resveratrol intraperitoneally (traditional IP slow bolus injection with a needle going either directly to the IP cavity or through an interscapular port implanted subcutaneously and connected to a catheter sutured in the muscle wall of the IP cavity) 16 hours before surgery. It is important to note that the type of IP injection (with or without a catheter) did not influence the outcomes observed; all animals receiving propylene glycol in their injections experienced a seizure.
During the preoperative injections (300 µL vehicle with 120 µL being propylene glycol), it was found that the rats began to have seizures within 2 minutes ± 1 minute. Presented in this case report is a series of retrospective case reports, describing seven rats that were evaluated in order to understand the acute toxicity occurring after the resveratrol administration (Table 1). Postmortem necropsy analysis was performed on the first rat that seized and died after resveratrol administration . All postmortem findings were normal. No gross abnormalities were identified at necropsy leading to a diagnosis of death due to status epilepticus. Etiology of seizure was undetermined but thought to be secondary to toxicity from resveratrol or diluent. There were no gross signs of abdominal inflammation, infection, or organ dysfunction secondary to injections through injection port. Ingesta in stomach and normal organs supports diagnosis of acute/peracute death without preexisting pathology. The lung lesions found were likely agonal in origin.
A second rat experienced status epilepticus following resveratrol administration. Since this was the second rat to experience seizures following administration of the drug, it was hypothesized that the animals could be suffering from seizures due to hypoglycemia resulting from the metabolism of the propylene glycol diluent in the drug. Therefore, 50% dextrose was administered to the seizing animal in order to diagnose the hypoglycemia and potentially prevent future seizures. It was found that 50% dextrose delivered orally (0.5 mL) or rectally (1.0 mL) within two minutes of initial tremors was able to stop the seizures 3 ± 2 minutes from dextrose administration time in 80% of the rats. Depending on the severity of the tremors, some of the animals were unable to receive the dextrose orally and would need to have it administered rectally.
Blood glucose levels were measured from either the tail or toe nail of one rat that had not received any prior resveratrol injections . Healthy rat blood glucose levels are measured to be 50–135 mg/dL. The blood glucose level of the rat prior to resveratrol injections was measured to be 125 mg/dL. At the time of initial seizing, blood glucose levels dropped to 106 mg/dL; however they kept rising during the seizing episode, reaching a stable level of 165 mg/dL. Administration of 50% dextrose orally and rectally was able to stop the seizures and a final blood glucose level of 236 mg/dL was measured once the animal had recovered. The results from the glucose tests indicated the animals were not hypoglycemic and the activation of the seizures was due to the compound being injected.
To understand which of the substances in the drug compound was the cause of the seizures, tests were performed evaluating the diluent, as well as each separate component of the diluent. When either the diluent, 40 : 60 propylene glycol/corn oil, or 100% propylene glycol was administered intraperitoneally to the rats, the animals began to seize within 1.5 minutes. However, when 100% corn oil was injected intraperitoneally into a rat, there were no seizures observed. It was concluded that propylene glycol was the trigger of the seizures to this particular set of rats.
Cardiac puncture was performed to draw blood directly from the heart of a rat that seized . The animal was anesthetized with isoflurane prior to the cardiac puncture. Sodium levels were 137 mmol/L with potassium at 5.6 mmol/L, due to acidosis from the ion shifts (Table 2). Furthermore, the blood work showed high levels of bilirubin and spherocytes indicating hemolysis (Table 2). The combined findings support a diagnosis of hemolysis and lactic acidosis, which may have led to the seizures, all of which appeared to be a consequence of the propylene glycol administration.
The implication of this report is that propylene glycol, which is a commonly used diluent for water insoluble substances used for parenteral administration, can be acutely toxic to some lines of rats. The objective of this study is not to describe successful treatment of this toxicity, but only to describe that it can occur. The dextrose was initially administered after the onset of seizures because it was thought that the seizures were related to hypoglycemia. Absorption from the oral or rectal mucosa was prompt and seizures ceased within minutes in animals that were going to respond. However, the hypothesis that the seizures were caused by hypoglycemia was later shown to be false, in which case the cause of the seizures was investigated and concluded to be due to the propylene glycol.
The current case of unexpected status epilepticus is thought to be specifically due to an error in the metabolic pathway of propylene glycol. In human adults, propylene glycol is estimated to be eliminated at ~45% by renal route and ~55% through hepatic metabolism through lactate and pyruvate [2, 16]. Similar metabolic pathways are found in rodents such as rats and mice [15, 17]. The mammalian metabolic pathway for propylene glycol (also known as monopropylene glycol or MPG) ultimately results in the formation of pyruvate, carbon dioxide, water, and potentially glucose (Figure 1). Oxidation of propylene glycol by alcohol dehydrogenase (ALDH) leads to lactaldehyde, which gets further broken down into methylglyoxal or lactate [5, 15]. Lactate then enters either the Krebs cycle or gluconeogenesis [5, 15]. The activation of gluconeogenesis results in production of glucose, which astrocytes then convert into polymerized glycogen [5, 15, 18]. The accumulation of gluconeogenesis and glycogen will deprive neurons of energy, which may alter neuronal function and results in epileptic-like activity [18, 19]. We suspect that the gluconeogenesis pathway may have been activated in our rats which resulted in status epilepticus. The suspicion of the gluconeogenesis pathway activation is further supported by the incidents of which administration of 50% dextrose to the seizing rats was able to stop the tremors. Schauwecker found that glucose rescue can diminish the extent of seizure induced cell death . In fact, they believed a deficiency of insulin signaling may have been the factor of seizure induced cell death .
Developmental issues and age in both humans and rats may result in complications when using drugs or food containing propylene glycol [1, 3, 14, 21–23]. Administration of pharmaceuticals containing 300 mg–3 g of propylene glycol per day for 14 days to premature newborn babies resulted in rapid progression of hyperbilirubinemia, seizures, and renal failure . Infants who experience seizures due to propylene glycol exposure are believed to likely have undeveloped metabolizing capability and high blood levels of propylene glycol [6, 22]. Thus, if either a human or rodent lacks the capacity to fully break down propylene glycol, negative side effects such as seizures are much more likely.
Toxicity in otherwise healthy humans and rodents of propylene glycol is based on accumulation and concentration. Several adverse effects have occurred following topical, oral, and intravenous administration [1, 21, 24, 25]. Some of these effects include central nervous system toxicity, hemolysis, hyperosmolarity, cardiac arrhythmia, and lactic acidosis [1, 26–29]. In experimental animals, propylene glycol has caused comas, seizures, circulatory collapse, ventricular dysrhythmias, and hypotension . Therefore, it may be detrimental to follow the guidelines of a known lethal dose of 13 g/kg administered intravenously for rats in order to avoid possible adverse side effects [4, 30]. It is important to note that the animals used in our study got a calculated maximum 0.52 g/kg (25 times lower dose). It is also noteworthy to mention that the volume of propylene glycol injected intraperitoneally in the rats described in this case report was no more than 120 µL. Volumes up to 500 µL of propylene glycol have been shown to be safely administered intraperitoneally to rats without any reported seizure like side effects [31, 32].
In conclusion, this report describes unexpected status epilepticus observed in the latest shipment of Sprague Dawley rats. The seizures were initiated after 300 µL ± 50 µL IP administration of resveratrol in a 40 : 60 propylene glycol/corn oil vehicle solution (equivalent to 0.52 g/kg of propylene glycol). None of the ongoing animals in the study experienced any seizure as side effects to the injections. The concentration and volume of propylene glycol were in accordance with previous toxicology limits. Thus, we conclude this phenomenon is likely due to(1)issues in the metabolic pathway of propylene glycol including (i) missing enzymes for lactate and/or pyruvate breakdown, (ii) activation of the gluconeogenesis pathway, or (iii) toxicity secondary to lactic acidosis,(2)underdeveloped or premature rats who went undiagnosed,(3)predisposition to epilepsy.The current findings correlate with other rodent and human pathologies to propylene glycol. This report appears to be the first published case of unexpected status epilepticus due to an IP injection containing propylene glycol. Moreover, to our knowledge this is the first reported case in which animals from an ongoing study have spontaneous adverse side effects halfway through a study.
Surgical procedures and animal care practices were performed in accordance with the Louis Stokes Cleveland Department of Veterans Affairs Institutional Animal Care and Use Committee (IACUC).
The contents do not represent the views of the US Department of Veterans Affairs of the United States Government.
Conflicts of Interest
The authors declare that there are no conflicts of interest regarding the publication of this article.
This study was supported by Merit Review Award no. B1495-R (Capadona), Presidential Early Career Award for Scientist and Engineers (PECASE, Capadona), and Career Development Award 1 (CDA-1, Ereifej) no. 11800342 from the United States Department of Veterans Affairs Rehabilitation Research and Development Service.
- T. Y. Lim, R. L. Poole, and N. M. Pageler, “Propylene glycol toxicity in children,” J Pediatr Pharmacol Ther, vol. 19, no. 4, pp. 277–282, 2014.
- A. Kulo, A. Smits, G. Naulaers, J. De Hoon, and K. Allegaert, “Biochemical tolerance during low dose propylene glycol exposure in neonates: a formulation-controlled evaluation,” DARU, Journal of Pharmaceutical Sciences, vol. 20, no. 1, no. 5, 2012.
- K. C. Wilson, C. Reardon, A. C. Theodore, and H. W. Farber, “Propylene glycol toxicity: A severe iatrogenic illness in ICU patients receiving IV benzodiazepines: a case series and prospective, observational pilot study,” Chest, vol. 128, no. 3, pp. 1674–1681, 2005.
- I. F. Gaunt, F. M. B. Carpanini, P. Grasso, and A. B. G. Lansdown, “Long-term toxicity of propylene glycol in rats,” Food and Cosmetics Toxicology, vol. 10, no. 2, pp. 151–162, 1972.
- J. A. Ruddick, “Toxicology, metabolism, and biochemistry of 1,2-propanediol,” Toxicology and Applied Pharmacology, vol. 21, no. 1, pp. 102–111, 1972.
- D. G. Clark and M. H. Litchfield, “The toxicity, metabolism, and pharmacologic properties of propylene glycol 1,2-dinitrate,” Toxicology and Applied Pharmacology, vol. 15, no. 1, pp. 175–184, 1969.
- B. J. Barnes, C. Gerst, J. R. Smith, A. R. Terrell, and M. E. Mullins, “Osmol gap as a surrogate marker for serum propylene glycol concentrations in patients receiving lorazepam for sedation,” Pharmacotherapy, vol. 26, no. 1, pp. 23–33, 2006.
- J. L. Nelsen, C. E. Haas, B. Habtemariam et al., “A prospective evaluation of propylene glycol clearance and accumulation during continuous-infusion lorazepam in critically ill patients,” Journal of Intensive Care Medicine, vol. 23, no. 3, pp. 184–194, 2008.
- J. C. Chen, Y. Chen, J. H. Lin, J. M. Wu, and S. H. Tseng, “Resveratrol suppresses angiogenesis in gliomas: evaluation by color Doppler ultrasound,” Anticancer Research, vol. 26, no. 2A, pp. 1237–1245, 2006.
- J. H. Jeong, Y. R. Lee, H. G. Park, and W. L. Lee, “The effects of either resveratrol or exercise on macrophage infiltration and switching from M1 to M2 in high fat diet mice,” The Journal of Exercise Nutrition and Biochemistry, vol. 6, no. 1, pp. 65–72, 1975.
- M. M. Oh, J. M. Power, L. T. Thompson, and J. F. Disterhoft, “Caution against using propylene glycol as a solvent in epilepsy drug research,” Neuroscience Research Communications, vol. 27, no. 2, pp. 117–124, 2000.
- D. L. Beckman and D. J. Crittenden, “Protection from Oxygen-Induced Seizures by Clonazepam and Propylene Glycol (41232),” Proceedings of the Society for Experimental Biology and Medicine, vol. 168, no. 1, pp. 45–48, 1981.
- B. W. M. M. Peeters, K. S. Cheung, J. M. H. Vossen, and A. M. L. Coenen, “Some solvents for antiepileptics have proepileptic potencies in the WAG/Rij rat model for absence epilepsy,” Brain Research Bulletin, vol. 29, no. 3-4, pp. 515–517, 1992.
- M. Bulathsinghala, K. Keefer, and A. Van De Louw, “Trimethoprim/Sulfamethoxazole-Induced Severe Lactic Acidosis,” Medicine (United States), vol. 95, no. 17, Article ID e3478, 2016.
- J. R. Fowles, M. I. Banton, and L. H. Pottenger, “A toxicological review of the propylene glycols,” Critical Reviews in Toxicology, vol. 43, no. 4, pp. 363–390, 2013.
- P. A. J. Speth, T. B. Vree, N. F. Neilen et al., “Propylene glycol pharmacokinetics and effects after intravenous infusion in humans,” Therapeutic Drug Monitoring, vol. 9, no. 3, pp. 255–258, 1987.
- “NTP-CERHR Expert Panel report on the reproductive and developmental toxicity of propylene glycol,” Reproductive Toxicology, vol. 18, no. 4, pp. 533–579, 2004.
- J.-F. Cloix and T. Hévor, “Epilepsy, regulation of brain energy metabolism and neurotransmission,” Current Medicinal Chemistry, vol. 16, no. 7, pp. 841–853, 2009.
- T. K. Hevor, P. Delorme, and J. C. Beauvillain, “Glycogen synthesis and immunocytochemical study of fructose-1,6-biphosphatase in methionine sulfoximine epileptogenic rodent brain,” Journal of Cerebral Blood Flow and Metabolism, vol. 6, no. 3, pp. 292–297, 1986.
- P. E. Schauwecker, “The effects of glycemic control on seizures and seizure-induced excitotoxic cell death,” BMC Neuroscience, vol. 13, no. 1, article no. 94, 2012.
- A. M. Glasgow, R. L. Boeckx, M. K. Miller, M. G. MacDonald, G. P. August, and S. I. Goodman, “Hyperosmolality in small infants due to propylene glycol,” Pediatrics, vol. 72, no. 3, pp. 353–355, 1983.
- M. G. MacDonald, “Propylene glycol: increased incidence of seizures in low birth weight infants,” Pediatrics, vol. 79, no. 4, p. 622, 1987.
- L. Hansen, R. Lange, and S. Gupta, “Development and evaluation of a guideline for monitoring propylene glycol toxicity in pediatric intensive care unit patients receiving continuous infusion lorazepam,” The Journal of Pediatric Pharmacology and Therapeutics, vol. 20, no. 5, pp. 367–372, 2015.
- G. Martin and L. Finberg, “Propylene glycol: a potentially toxic vehicle in liquid dosage form,” The Journal of Pediatrics, vol. 77, no. 5, pp. 877-878, 1970.
- K. Arulanantham and M. Genel, “Central nervous system toxicity associated with ingestion of propylene glycol,” Journal of Pediatrics, vol. 93, no. 3, pp. 515-516, 1978.
- O. L. Hung and L. Nelson, Tintinalli's Emergency Medicine: A Comprehensive Study Guide, McGraw-Hill, New York, NY, USA, 2004.
- K. A. Tuohy, W. J. Nicholson, and F. Schiffman, “Agitation by sedation,” Lancet, vol. 361, no. 9354, p. 308, 2003.
- M. J. Kelner and D. N. Bailey, “Propylene glycol as a cause of lactic acidosis,” Journal of Analytical Toxicology, vol. 9, no. 1, pp. 40–42, 1985.
- J. O'Donnell, S. L. Mertl, and W. N. Kelly, “Propylene glycol toxicity in a pediatric patient: the dangers of diluents,” Journal of Pharmacy Practice, vol. 13, no. 3, pp. 214–225, 2000.
- W. Spector, Handbook of Toxicology Vol 1 Acute Toxicities of Solds, Liquids and Gases to Laboratory Animals, Saunders, 1956.
- J. F. Turrens, J. Lariccia, and M. G. Nair, “Resveratrol has no effect on lipoprotein profile and does not prevent peroxidation of serum lipids in normal rats,” Free Radical Research, vol. 27, no. 6, pp. 557–562, 1997.
- S.-H. Tseng, S.-M. Lin, J.-C. Chen et al., “Resveratrol suppresses the angiogenesis and tumor growth of gliomas in rats,” Clinical Cancer Research, vol. 10, no. 6, pp. 2190–2202, 2004.
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