Literature DB >> 3709502

Sulfolane-induced hypothermia enhances survivability in mice.

C J Gordon, M D Long, K S Fehlner, R S Dyer.   

Abstract

Mice injected intraperitoneally with sulfolane (tetrahydrothiophene-1,1-dioxide) underwent a significant decrease in metabolic rate and body temperature at ambient temperatures of 20 and 30 degrees C but not 35 degrees C. If given the opportunity, mice treated with sulfolane preferentially sought a cool ambient temperature. When given an LD50 dose of sulfolane (1270 mg/kg), the percentage mortality varied directly with ambient temperature. For example, at 35 degrees C mortality was 75% whereas at 25 degrees C mortality was only 8%. By undergoing an autonomically and behaviorally mediated decrease in body temperature (i.e., regulated hypothermia), sulfolane-treated mice appear to enhance their chance of survival.

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Year:  1986        PMID: 3709502     DOI: 10.1016/s0013-9351(86)80084-6

Source DB:  PubMed          Journal:  Environ Res        ISSN: 0013-9351            Impact factor:   6.498


  4 in total

1.  Thermoregulatory responses of the rabbit to subcutaneous injection of sulfolane.

Authors:  F S Mohler; C J Gordon
Journal:  Arch Toxicol       Date:  1988       Impact factor: 5.153

2.  Toxicokinetics and bioavailability of sulfolane, a ground water contaminant, following oral and intravenous administration in rodents: A dose, species, and sex comparison.

Authors:  Suramya Waidyanatha; Sherry R Black; Timothy R Fennell; Scott L Watson; Purvi R Patel; Stephen D Cooper; James Blake; Veronica Godfrey Robinson; Reshan A Fernando; Chad R Blystone
Journal:  Toxicol Appl Pharmacol       Date:  2019-07-22       Impact factor: 4.219

3.  Health Impact Assessment of Sulfolane on Embryonic Development of Zebrafish (Danio rerio).

Authors:  Soham M Shah; Michael Wahba; Linlong Yu; Gopal Achari; Hamid R Habibi
Journal:  Toxics       Date:  2019-08-23

4.  Comparison of sulfolane effects in Sprague Dawley rats, B6C3F1/N mice, and Hartley guinea pigs after 28 days of exposure via oral gavage.

Authors:  K A Shipkowski; M C Cora; M F Cesta; V G Robinson; S Waidyanatha; K L Witt; M K Vallant; D M Fallacara; M R Hejtmancik; S A Masten; S D Cooper; R A Fernando; C R Blystone
Journal:  Toxicol Rep       Date:  2021-02-06
  4 in total

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