[ RadSafe ] uranium smoke is a teratogen
ROY HERREN
royherren2005 at yahoo.com
Tue May 27 17:56:26 CDT 2008
Steven,
I'm really quite surprised to read that "James Salsman has objected" to your not having read JL Domingo's paper, and yet he hasn't offered as of yet to share his copy of the full article with you. I appreciate the fact that you've experienced difficulties in acquiring this particular paper. As a reasonable solution to this dilemma, I humble suggest that since James Salsman allegedly has access to the full paper, and since he is so anxious for you to read this important paper that he should share his copy of the full paper with you and the rest of the Radsafe mailing list. Perhaps this e-mail may even serve to encourage James Salsman to take action towards generously sharing his copy of this paper with you and the rest of the Radsafe community. I am confident that the entire Radsafe community is looking forward to reading the paper in question shortly after James Salsman has made it available in a open e-mail text format.
Roy Herren
----- Original Message ----
From: Steven Dapra <sjd at swcp.com>
To: radsafelist <radsafe at radlab.nl>
Sent: Sunday, May 25, 2008 5:55:43 PM
Subject: Re: [ RadSafe ] uranium smoke is a teratogen
May 25
James Salsman has objected to my not having read JL Domingo's
paper "Reproductive and developmental toxicity of natural and depleted
uranium: a
review." [Reprod Toxicol. 2001 Nov-Dec;15(6):603-9.]
The abstract of this paper reads: "Although the biokinetics,
metabolism, and chemical toxicity of uranium are well known, until recently
little attention was paid to the potential toxic effects of uranium on
reproduction and development in mammals. In recent years, it has been
shown that uranium is a developmental toxicant when given orally or
subcutaneously (SC) to mice. Decreased fertility, embryo/fetal toxicity
including teratogenicity, and reduced growth of the offspring have been
observed following uranium exposure at different gestation periods. The
reproductive toxicity, maternal toxicity, embryo/fetal toxicity, and
postnatal effects of uranium, as well as the prevention by chelating agents
of uranium-induced maternal and developmental toxicity are reviewed
here. Data on the toxic effects of depleted uranium on reproduction and
development are also reviewed."
Note that until recently little attention has been paid to the
uranium's possible adverse effects in mammals. That would tend to suggest
--- wouldn't it? --- that uranium isn't obviously injuring or killing
people or animals and that from the outset it might not be much of a health
problem. Epidemiologists probably tend to confine their studies to
substances or conditions that are having an obvious effect, or that can be
plausibly connected with some health outcome.
JL Domingo is popular with James Salsman/Ben Fore, and by doing a
Google search I was able to locate one abstract of a paper, and one full
text of a paper (each with JL Domingo as a co-author) on the effects of
uranium on mice, or on rats. (He is the last co-author listed on each of
the two papers.) I will discuss each of these items (briefly, I hope). At
the end of this message I will present the citations, links and so
forth. All citations have been omitted from my discussion.
Discussion of the ABSTRACT:
The title of the paper is "Influence of Chronic Exposure to
Uranium on Male Reproduction in Mice."
The study mice were treated with treated with five different doses
of uranyl acetate dihydrate that was added to their drinking water. "There
was a significant but non-dose-related decrease in the pregnancy rate of
these animals. Body weights were significantly depressed only" at one of
the dose rates. "The results of this investigation indicate that uranium
does not cause any adverse effect on testicular function in mice at the
concentrations usually ingested in the diet and drinking water, with a
safety factor of more than 1000."
Discussion of the PAPER (which was an "Original Research Article.")
The title of the paper is "Influence of Maternal Stress on
Uranium-Induced Developmental Toxicity in Rats."
From the Introduction: "Although uranium (U) exposure can result
in both chemical and radiological toxicity, in general, chemical toxic
effects from uranium compounds occur at lower exposure levels than
radiological toxicity." (That chemical effects are seen before
radiological effects is well known, however I believe it bears repeating.)
This study exposed pregnant Sprague-Dawley rats to uranyl acetate
dihydrate (UAD); and to stress, by restraining for rats for a certain
period of time each day.
(From the "Results.")
"No external, internal, or skeletal malformations, as well as
external and internal variations, which could be attributed to uranium
exposure or maternal immobilization were noted." Also: "Although in
relation to the control group the total number of fetuses with skeletal
defects was significantly increased by uranium exposure, this increase was
not dose-related."
(From the "Discussion.")
"However, in contrast to the results in mice no significant maternal
toxicity was noted in rats at 1/20 of the LD-50 (0.415 mg/kg/day)." The
significance of this is the different effect of the UAD on different
species. Could the UAD also have a different effect on humans that it does
on rats and mice? The paper again acknowledges the different effects (on
rats and mice), saying, "A comparison of the results of both studies
indicates that mice are more sensitive than rats to the toxic effects of
uranium during gestation."
The paper ends by saying:
"In summary, while the results of the present study in rats
corroborate only partly some of the adverse effects of uranium exposure
during gestation reported in mice, according to the overall data in both
species, the results indicated that uranium is a developmental toxicant in
mammals. Although most pregnant women are not currently exposed to uranium
levels that could cause adverse effects on health, higher rates of uranium
exposure have been reported for some populations (e.g., individuals who
consume foods grown in areas with elevated concentrations of uranium in the
soil, or subjects with elevated uranium levels in their drinking water). In
turn, the military use of DU might be of concern as an additional source of
exposure. On the other hand, if uranium exposures occur at levels that may
provoke maternal toxicity, the potential adverse developmental effects
could be enhanced by stress."
Other than to say that studies on humans would have to tease out
the effects of stress versus those of depleted uranium, there is no need to
comment.
Finally, since James Salsman/Ben Fore like to claim that depleted
uranium, uranyl, etc., cause birth defects, according to the abstract of
this paper, "No teratogenic effects were noted in any group." Let me
reiterate that this paper was co-authored by the JL Domingo whose paper in
Reproductive Toxicology James/Ben has on several occasions derided me for
not reading.
Steven Dapra
Link and publishing data for the Abstract:
<http://toxsci.oxfordjournals.org/cgi/content/abstract/16/4/821>
(1991) Fundam Appl. Toxicol. 16, 821829.
Received July 24, 1990; accepted December 28, 1990
Influence of Chronic Exposure to Uranium on Male Reproduction in Mice
Juan M. Llobet, Juan J. Sirvent, Arturo Ortega, and Jose L Domingo.
Laboratory of Toxicology and Biochemistry San Lorenzo 21, 43201 Reus, Spain
Pathology Unit, School of Medicine, University of Barcelona San Lorenzo 21,
43201 Reus, Spain
Link and publishing data for the Original Research Article:
<http://www.ebmonline.org/cgi/content/full/228/9/1072>
Experimental Biology and Medicine 228:1072-1077 (2003)
Influence of Maternal Stress on Uranium-Induced Developmental Toxicity in Rats
M. Luisa Albina, Montserrat Belles, Mercedes Gomez, Domenec J. Sanchez and
Jose L. Domingo.
Laboratory of Toxicology and Environmental Health, School of Medicine,
"Rovira i Virgili" University, 43201 Reus, Spain
------- END -------
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