Vol. 282, Issue 6, R1544-R1544, June 2002
EDITORIAL
The mouse is a small rabbit
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ARTICLE |
Only a few years back in time, many of us would have viewed the
mouse, from a physiological point of view, to be a miniature rat. In
this month's issue, two reviews on murine physiology and experimental
techniques are published, and the authors share the opinion that this
is surely not the case (2, 3). In fact, Lorenz
(3) sees more similarities between the mouse and rabbit than between the mouse and rat. The mouse, like the rabbit, is extremely sensitive to anesthesia and has labile blood pressure control. Legend has it that Kurt Kramer once claimed rabbits are flowers, not animals. In a table "of mice and men," Janssen and Smits (2) provide a comparison of several human
physiological parameters with those found for this increasingly popular
rodent. Even within individual mouse strains, genetic diversity is
rich. For instance, several articles in the American Journal of
Physiology-Regulatory, Integrative and Comparative Physiology have
shed light on interstrain particularities (1, 4, 5). As
highlighted by Janssen and Smits (2), a fully new
nomenclature was required to simply discern the various parental lines
of the 129 mouse from related strains. The spreading interest in mouse
models has led to several web sites providing useful information
regarding data analysis, nomenclature, anatomy, and autopsy of the
mouse. Several of these sites are now provided in their review.
The main emphasis of the overview by Janssen and Smits (2)
is related to murine autonomic nervous control of circulation. One
interesting conclusion is that mice might be particularly suited as
models for diseases related to enhanced sympathetic activity, because
mice reveal high levels of the prevailing sympathetic tone.
Lorenz (3) focuses more on technical aspects, in
particular with regard to anesthesia, cardiovascular, renal, and
pulmonary techniques. With these two expert overviews, we hope to
bridge the gap between those generating mice models and those
exploiting them.
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FOOTNOTES |
10.1152/ajpregu.00158.2002
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REFERENCES |
1.
Harris, RB,
Mitchell TD,
Yan X,
Simpson JS,
and
Redmann SM, Jr.
Metabolic responses to leptin in obese db/db mice are strain dependent.
Am J Physiol Regulatory Integrative Comp Physiol
281:
R115-R132,
2001[Abstract/Free Full Text].
2.
Janssen, BJA,
and
Smits JFM
Autonomic control of blood pressure in mice: basic physiology and effects of genetic modification.
Am J Physiol Regulatory Integrative Comp Physiol
282:
R1545-R1564,
2002[Abstract/Free Full Text].
3.
Lorenz, JN.
A practical guide to evaluating cardiovascular, renal, and pulmonary function in mice.
Am J Physiol Regulatory Integrative Comp Physiol
282:
R1565-R1582,
2002[Abstract/Free Full Text].
4.
Meerlo, P,
Easton A,
Bergmann BM,
and
Turek FW.
Restraint increases prolactin and REM sleep in C57BL/6J mice but not in BALB/cJ mice.
Am J Physiol Regulatory Integrative Comp Physiol
281:
R846-R854,
2001[Abstract/Free Full Text].
5.
Smith, BK,
Volaufova J,
and
West DB.
Increased flavor preference and lick activity for sucrose and corn oil in SWR/J vs. AKR/J mice.
Am J Physiol Regulatory Integrative Comp Physiol
281:
R596-R606,
2001[Abstract/Free Full Text].
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Pontus B. Persson, Editor
American Journal of Physiology-Regulatory, Integrative and
Comparative Physiology June 2002, Volume 282
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Am J Physiol Regul Integr Comp Physiol 282(6):R1544-R1544
0363-6119/02 $5.00
Copyright © 2002 the American Physiological Society