Definition and research guide
This page combines a MeSH definition, publication statistics and selected research abstracts. It is a starting point for reading the literature, not a medical textbook or a systematic evidence review.
Content available: 3 complete abstracts (718 words), 8 references. Full article text is not stored or reproduced here; follow the PMID, DOI or PMC links to read the original sources and their access terms.
Definition
A derivative of chloral hydrate that was used as a sedative but has been replaced by safer and more effective drugs. Its most common use is as a general anesthetic in animal experiments.
Definition: NLM Medical Subject Headings (MeSH) scope note (Public domain (U.S. National Library of Medicine); attribution requested). View the MeSH record.
Also known as: alpha-Chloralose; alpha Chloralose; Anhydroglucochloral; Glucochloral; Glucochloralose; beta-Chloralose; beta Chloralose.
Where it fits in the MeSH classification
- Broader topics
- Chloral Hydrate; Glucosides
Related concepts
- Chloral Hydrate
Research landscape
PubMed indexes 1,193 records tagged with the MeSH heading “Chloralose” (counts retrieved 2026-10-31). 10 of them (0.8%) were published from 2020 onward, and the busiest period so far is through 1999 with 1,053 records.
Reviews account for 17 records (1.4%) and meta-analyses for 0. Randomized controlled trials number 0 (0.0%) as a share of all records on the topic. Randomized trials make up only a small share of this literature, so much of what is known comes from laboratory, observational or descriptive work.
Show the data
| Period | Records |
|---|---|
| through 1999 | 1,053 |
| 2000-2009 | 87 |
| 2010-2019 | 43 |
| 2020 onward | 10 |
Publication-type chart data
| Type | Records | Share |
|---|---|---|
| Reviews | 17 | 1.4% |
| Meta-analyses | 0 | 0.0% |
| Randomized controlled trials | 0 | 0.0% |
Method: PubMed query "Chloralose"[MeSH Terms] with publication-type and date filters, retrieved 2026-10-31.
Reading the evidence in drugs and chemicals
Studies of a chemical or drug can answer very different questions: what it is and how it behaves in cells and animals, how the body handles it, and whether it changes outcomes in people. Laboratory and animal findings often do not carry over to patients, and observational studies of exposures are confounded by who uses a substance and why. Nothing on this page is a recommendation to use, avoid, start or stop any substance or medicine; talk to a qualified clinician or pharmacist about your own situation. Check the dose, the species, the comparison group and whether a patient-relevant outcome was measured.
Evidence from open-access studies
These open-access studies come from PubMed’s best-match results for this heading (papers whose main topic it is), ranked here by citation count, with one recent addition. Each abstract is reproduced in full under its recorded open licence so that you can read the authors’ own words. They illustrate the literature; they are not a systematic summary of it. Citation counts measure attention, not reliability or clinical benefit.
| Study / authors | Year | Source label / design | Europe PMC citations | Licence / source |
|---|---|---|---|---|
| Comparing the Effects of Isoflurane and Alpha Chloralose upon Mouse Physiology | 2016 | Research article Design not recorded in structured metadata | 45 | cc0 PMID 27148970 · DOI · PMC4858227 |
| Stability of the acetic acid-induced bladder irritation model in alpha chloralose-anesthetized female cats | 2013 | Research article Design not recorded in structured metadata | 14 | cc by PMID 24040064 · DOI · PMC3767621 |
| Alpha-chloralose poisoning in cats: clinical findings in 25 confirmed and 78 suspected cases | 2022 | Research article Design not recorded in structured metadata | 3 | cc by PMID 35757929 · DOI · PMC9510939 |
Comparing the Effects of Isoflurane and Alpha Chloralose upon Mouse Physiology [1]
Abstract reading summary — source excerpts
- Opening excerpt
- Functional magnetic resonance imaging of mice requires that the physiology of the mouse (body temperature, respiration and heart rates, blood pH level) be maintained in order to prevent changes affecting the outcomes of functional scanning, namely blood oxygenation level dependent (BOLD) measures and cerebral blood flow (CBF).
- Closing excerpt
- We suggest that alpha chloralose does not maintain normal mouse physiology adequately for functional brain imaging outcome measures.
- Interpretation limits
- Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (179 words)
Functional magnetic resonance imaging of mice requires that the physiology of the mouse (body temperature, respiration and heart rates, blood pH level) be maintained in order to prevent changes affecting the outcomes of functional scanning, namely blood oxygenation level dependent (BOLD) measures and cerebral blood flow (CBF). The anesthetic used to sedate mice for scanning can have major effects on physiology. While alpha chloralose has been commonly used for functional imaging of rats, its effects on physiology are not well characterized in the literature for any species. In this study, we anesthetized or sedated mice with isoflurane or alpha chloralose for up to two hours, and monitored physiological parameters and arterial blood gasses. We found that, when normal body temperature is maintained, breathing rates for both drugs decrease over the course of two hours. In addition, alpha chloralose causes a substantial drop in heart rate and blood pH with severe hypercapnia (elevated blood CO2) that is not seen in isoflurane-treated animals. We suggest that alpha chloralose does not maintain normal mouse physiology adequately for functional brain imaging outcome measures.
Abstract reproduced from the open-access article under the recorded cc0 licence; © the authors. PMID 27148970 · DOI · PMC4858227
Stability of the acetic acid-induced bladder irritation model in alpha chloralose-anesthetized female cats [2]
Abstract reading summary — source excerpts
- Opening excerpt
- Time- and vehicle-related variability of bladder and urethral rhabdosphincter (URS) activity as well as cardiorespiratory and blood chemistry values were examined in the acetic acid-induced bladder irritation model in α-chloralose-anesthetized female cats.
- Closing excerpt
- These data provide an ample evaluation of the health of the animals, stability of voiding function and appropriateness of the model for testing drugs designed to evaluate lower urinary tract as well as cardiovascular and respiratory systems function.
- Interpretation limits
- Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (246 words)
Time- and vehicle-related variability of bladder and urethral rhabdosphincter (URS) activity as well as cardiorespiratory and blood chemistry values were examined in the acetic acid-induced bladder irritation model in α-chloralose-anesthetized female cats. Additionally, bladder and urethra were evaluated histologically using Mason trichrome and toluidine blue staining. Urodynamic, cardiovascular and respiratory parameters were collected during intravesical saline infusion followed by acetic acid (0.5%) to irritate the bladder. One hour after starting acetic acid infusion, a protocol consisting of a cystometrogram, continuous infusion-induced rhythmic voiding contractions, and a 5 min "quiet period" (bladder emptied without infusion) was precisely repeated every 30 minutes. Administration of vehicle (saline i.v.) occurred 15 minutes after starting each of the first 7 cystometrograms and duloxetine (1mg/kg i.v.) after the 8(th). Acetic acid infusion into the bladder increased URS-EMG activity, bladder contraction frequency, and decreased contraction amplitude and capacity, compared to saline. Bladder activity and URS activity stabilized within 1 and 2 hours, respectively. Duloxetine administration significantly decreased bladder contraction frequency and increased URS-EMG activity to levels similar to previous reports. Cardiorespiratory parameters and blood gas levels remained consistent throughout the experiment. The epithelium of the bladder and urethra were greatly damaged and edema and infiltration of neutrophils in the lamina propria of urethra were observed. These data provide an ample evaluation of the health of the animals, stability of voiding function and appropriateness of the model for testing drugs designed to evaluate lower urinary tract as well as cardiovascular and respiratory systems function.
Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 24040064 · DOI · PMC3767621
Alpha-chloralose poisoning in cats: clinical findings in 25 confirmed and 78 suspected cases [3]
Abstract reading summary — source excerpts
- Opening excerpt
- ObjectivesThe aim of this study was to describe the clinical picture in cats with alpha-chloralose (AC) intoxication and to confirm AC in serum from suspected cases of AC poisoning.
- Closing excerpt
- A severe clinical picture upon presentation could be misinterpreted as a grave prognosis and awareness about AC poisoning may avoid unnecessary euthanasia.
- Interpretation limits
- Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (293 words)
ObjectivesThe aim of this study was to describe the clinical picture in cats with alpha-chloralose (AC) intoxication and to confirm AC in serum from suspected cases of AC poisoning.MethodsSuspected cases of AC poisoning were identified in patient records from a small animal university hospital from January 2014 to February 2020. Clinical signs of intoxication described in respective records were compiled, the cats were graded into four intoxication severity scores and hospitalisation time and mortality were recorded. Surplus serum from select cases in late 2019 and early 2020 was analysed to detect AC with a quantitative ultra-high performance liquid chromatography tandem mass spectrometry analysis, and the AC concentration was compared with the respective cat's intoxication severity score.ResultsSerum from 25 cats was available for analysis and AC poisoning was confirmed in all. Additionally, 78 cats with a clinical suspicion of AC intoxication were identified in the patient records, most of which presented from September to April. The most common signs of intoxication were ataxia, tremors, cranial nerve deficits and hyperaesthesia. The prevalence of clinical signs and intoxication severity differed from what has previously been reported, with our population presenting with less severe signs and no deaths due to intoxication. The majority had a hospitalisation time Conclusions and relevanceThis study describes the clinical signs and prognosis in feline AC intoxication. There were no mortalities in confirmed cases, indicating that AC-poisoned cats have an excellent prognosis when treated in a timely manner. Recognition of AC intoxication as a differential diagnosis for acute onset of the described neurological signs in areas where AC exposure is possible may influence clinical decision-making and help avoid excessive diagnostic procedures. A severe clinical picture upon presentation could be misinterpreted as a grave prognosis and awareness about AC poisoning may avoid unnecessary euthanasia.
Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 35757929 · DOI · PMC9510939
Key reviews and meta-analyses
The most cited review-type papers among PubMed’s best-match results for this heading, listed with bibliographic details only. Follow the links for the full text and access terms.
- Research article The pharmacology of chloralose. A review [4]
- Research article A review of laboratory animal anesthesia with chloral hydrate and chloralose [5]
- Research article TELECEPTIVE COMPONENTS OF THE CEREBELLAR FUNCTION [6]
- Research article Alpha-chloralose as a canine anesthetic [7]
- Research article Pharmacology and toxicology of alpha chloralose: a review [8]
References
- Low LA, Bauer LC, Klaunberg BA. Comparing the Effects of Isoflurane and Alpha Chloralose upon Mouse Physiology. . 2016. PMID 27148970 · DOI · PMC4858227
- Kullmann FA, Wells GI, Langdale CL, Zheng J, Thor KB. Stability of the acetic acid-induced bladder irritation model in alpha chloralose-anesthetized female cats. . 2013. PMID 24040064 · DOI · PMC3767621
- Tegner C, Lundgren S, Dreimanis K, Åberg AT, Windahl U. Alpha-chloralose poisoning in cats: clinical findings in 25 confirmed and 78 suspected cases. . 2022. PMID 35757929 · DOI · PMC9510939
- Balis GU, Monroe RR. The pharmacology of chloralose. A review. Psychopharmacologia. 1964. PMID 5318644 · DOI
- Silverman J, Muir WW. A review of laboratory animal anesthesia with chloral hydrate and chloralose. Lab Anim Sci. 1993. PMID 8355479
- FADIGA E, PUPILLI GC. TELECEPTIVE COMPONENTS OF THE CEREBELLAR FUNCTION. Physiol Rev. 1964. PMID 14174152 · DOI
- Holzgrefe HH, Everitt JM, Wright EM. Alpha-chloralose as a canine anesthetic. Lab Anim Sci. 1987. PMID 3320515
- Lees P. Pharmacology and toxicology of alpha chloralose: a review. Vet Rec. 1972. PMID 4562133 · DOI
About this article
- Sources
- NLM Medical Subject Headings (definition, synonyms); NCBI PubMed (counts, identifiers); Europe PMC (open-access abstracts and citation counts).
- Verification
- Every reference was resolved against PubMed on 2026-10-31; title, year and DOI matched.
- Review state
- automated source verified; no human expert review has been recorded yet.
- Version
- 1, last updated 2026-10-31.
See how EvidenceLib is built. Spotted an error? Email support@evidencehelix.com.
Evidence strength
EvidenceHelix's computed view of the study designs behind this topic: how common meta-analyses, randomized trials and reviews are, how recent the literature is, and a plain-language reading. It describes the design mix of the literature. It is not a quality appraisal of any study, and it is not medical advice.