Evidence map›Paper›PMID 21178502›Full record

ArticleVirulence

Obesity, longevity, quality of life: alteration by dietary 2-mercaptoethanol.

Robert E Click

Abstract read
In one paragraph

Article in Virulence. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

1 author.

Robert E ClickVA Medical Center, Minneapolis, MN, USA. mbclicker@msn.com

Funding

CONTROL OF A COMPOSITE OF DIVERSE IMMUNE FUNCTIONSR01AI019643 · NIAID · UNIVERSITY OF MINNESOTA TWIN CITIES · PI CLICK, ROBERT E · 1985 to 1986
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NCI NIH HHS R01 CA023678NIAID NIH HHS R01AI019643
6 · The paper itself

Abstract

Previous investigations demonstrated that optimization of murine immunological reactivity in tissue culture required a sulfhydryl compound; the most effective being 2-mercaptoethanol (2-Me). Since these reports, 2-Me was found beneficial for both growth/function of other cell-types in vitro, including those of other species, and when fed orally, it impeded and/or reversed some in situ physiological changes associated with aging. More recently, thiol-containing compounds possessing oxidation-reduction potentials weaker than 2-Me were found to impart beneficial effects for many other, including human, diseases. Based on these effects, the research herein addressed the question: What consequences might dietary 2-Me impart on health and disease of mice other than those associated with aging? The main parameters monitored over the lifetime of individual animals exposed to dietary 10⁻³ M 2-Me in their drinking water were: quality of life (obesity and development of recumbent, emaciated and/or cachectic health); longevity; and appearance of tumors. Instead of anticipated toxic attributes, the following unique benefits were found; mean survival of a moderately-lived strain (A/J) was increased 40.8%, high-fat-diet obesity was curtailed in C57BL/10 mice, and a goal of aging intervention protocols, namely preventing loss of quality of life during aging (recumbent, emaciated and/or cachectic) was achieved. Various mechanisms are discussed as they pertain to these findings.

Indexed as

AnimalsDietFemaleLongevityMaleMercaptoethanolMiceMice, Inbred C57BLNeoplasmsObesityMercaptoethanol

Identifiers

PMID21178502
PMCPMC3073360

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.