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Centennial Perspectives
Centennial Perspectives are short
review, or perspective articles, on important topics in pharmacology
and therapeutics summarizing the development of knowledge on the
topic over the last century.
Centennial Perspectives will appear
in all of ASPET's journals over the course of the next two years and
will be freely available online immediately after publication.
If you would like to write a Centennial Perspective, please contact
Richard Dodenhoff, ASPET's Journals Director,
rdodenhoff@aspet.org.

The Singular Moral Compass of Otto Krayer
Molecular Interventions 5: 324-329 (2005)
Rebecca Anderson, Early Development
Operations, Amgen, Inc.
On June 15, 1933, Otto Krayer sat down to write the
most important letter of his professional career. The
thirty-three-year-old clinical scientist had just been
offered the chair of pharmacology and toxicology at the
Medical Academy of Düsseldorf, and everyone expected
Krayer to accept the appointment. He declined. "I will
abstain from winning a position that corresponds to my
inclinations and abilities," he wrote, "rather than make
a decision contrary to my conviction or, by remaining inauspiciously
silent, further an opinion about me that is not in accordance
with the facts." Krayer saw the removal of the Jewish
incumbent chairman, Philipp Ellinger, to be an injustice
that he explicitly challenged. "Under these
circumstances, assuming such a position as the one in
Düsseldorf would impose a great mental burden on me," he
explained. Krayer was the sole scientist to decline the
"call" (as it is said in German) to a chaired position that,
in accordance with Nazi law, could no longer be occupied by
a Jew. Krayer’s moral stand, so carefully and
thoughtfully considered, enraged the German authorities.
The sanctions they imposed, banning him from teaching or
even using university libraries, effectively ended his
promising academic career in Germany. Contemporaries of
Krayer who faced similar censorship were driven to become
vocal political dissidents. Otto Krayer, on the other
hand, did not enter into external, political discourse,
and chose rather to leave his homeland in order to pursue his
interests in pharmacology. He went on to lead a highly
productive professional life, in the sphere of science,
that was always guided by an uncompromising moral
compass.

Torald Sollmann's Studies
of Mustard Gas
Molecular Interventions 7:124-128 (2007)
Brian M. Cox, Professor, Dept of Pharmacology,
Uniformed Services University of the Health Sciences
In 1919, Torald Sollmann published
two papers in the on the ability of selected solvents and
absorbents to modify the severity of skin lesions induced
by mustard gas (1,1'-thiobis[2-chlorethane], or
dichloroethyl sulfide). Mustard gas, or sulfur mustard, is
a vesicating agent that had recently been used on troops
fighting in the First World War. Sollmann’s studies were
unusual, at least by today’s standards, in that he chose
to study the effects of this highly toxic compound on
himself and on students who volunteered for the project.
These studies did not provide insights into the mechanism
of action of mustard gas or lead to the introduction of a
novel antidote, and they certainly do not count among the
major contributions to pharmacological research that
arose from Sollmann’s long and distinguished career.
Nevertheless, the papers are of interest because they
shed light on the way that pharmacology was practiced by one
of the founding members of the American Society for
Pharmacology and Experimental Therapeutics. The
willingness of Sollmann to expose both himself and his
students to significant personal risk in the search for
protective measures against mustard gas may also reflect
the sense of fear and concern in the public at the use of
chemical warfare in the twentieth century.
The
Development of Drug Metabolism Research as Expressed in the
Publications of ASPET: Part 1,1909-1958
Drug Metabolism and Disposition,
36: 105 (2008)
Patrick J. Murphy,
Butler University
This is the first
of three articles covering the development of drug metabolism
research in the US during the first 100 years of ASPET. Prior to
1909 the majority of drug metabolism research was performed in
Europe. The period from 1909-1958 saw extensive development of the
methods required for modern metabolism studies. Examples of trends
and specific discoveries are drawn from the archives of ASPET
publications.
The Development of Drug
Metabolism Research as Expressed in the Publications of ASPET,
Part 2 - 1959-1983
Drug
Metabolism and Disposition,
36: 981 (2008)
Patrick Murphy,
Butler University
In 25 years
drug metabolism research went from using sub cellular
particles of undefined content to an understanding of metabolism
at the molecular level. The discovery of cytochrome P450,
enzyme induction, reactive intermediates, and genetic
polymorphisms provided milestones in the field. New
publications from ASPET chronicled the discoveries
and provided communications to advance the science of
drug metabolism.
The Development of Drug
Metabolism Research as Expressed in the Publications of ASPET,
Part 3 - 1984-2008,
Drug Metabolism and Disposition,
36: 1977 (2008)
Patrick Murphy,
Butler University
The dramatic changes in drug metabolism research in the last 25
years are well documented in the publications of ASPET.
New analytical tools combined with modern molecular biological
techniques have provided unprecedented access to the workings of
the cell. A field that concentrated on only a handful of
primary enzymes now has a list of hundreds in its purview.
Genetic variation, environmental impact, and molecular diversity
have all come under study in attempts to follow the fate of
drugs and chemicals. Examples from ASPET journals will be
used to illustrate the dramatic advancements in the field.
A
Brief History of Great Discoveries in Pharmacology: In
Celebration of the Centennial Anniversary of the Founding of the
American Society of Pharmacology and Experimental Therapeutics
Pharmacological Reviews, 59: 289-359 (2007)
Ronald P. Rubin,
Professor and Chair, Dept of Pharmacology &
Toxicology, SUNY-Buffalo Medical School
When the American Society of
Pharmacology and Experimental Therapeutics (ASPET1)
Centennial Committee began considering ways to celebrate
the Society's 100th anniversary in 2008, an early interest
was expressed in having a publication that presented
the research history of the discipline. However, the
Committee recognized that such a tome would fill a
very large volume and be an immense task.
Several problems were perceived. First, it
would take an enormous effort, one which few authors
would be willing to undertake. Second, the likelihood
that a quality publication of that magnitude could be
produced by 2008 was slight. Third, no matter how thorough
an author might be, the work of many excellent
pharmacologists would be omitted and could lead to
conflicts. Finally, possibly the most important
problem would be that the shear mass of material
would not attract many young pharmacologists as readers. More
than anything else, the Centennial Committee wants this
publication to be interesting to young scientists.
It came to the attention of the Committee that
Dr. Ronald Rubin had been independently considering
writing about key discoveries in the history of
pharmacology. The Committee offered to sponsor the
project. What follows is the outcome of that effort by Dr.
Rubin. In the view of the Committee, what Dr. Rubin has
written avoids the major problems noted above.
The history is written in a highly interesting
vein and is of a length that can be read in a
relatively short period of time. The theses chosen
are of such importance and are developed in such a
style that it would be difficult to fault their selection.
The lead investigators that Dr. Rubin highlights were (or
are) remarkable individuals. Although each discovery
discussed herein culiminated in a Nobel Prize, many
other familiar names are woven into the fabric, and
the evolution of ideas from multiple individuals is
emphasized.
The Centennial Committee is pleased to sponsor
this publication and hopes that the memories of more
senior scientists will be relived and that young
scientists will find the stories inspiring. We give
our thanks to Dr. Rubin for his efforts and for these
fine results.
William W. Fleming on behalf of the Centennial Committee

A Brief History of ASPET on Its Centennial Anniversary
Molecular Interventions, 7: 288-302 (2007)
John Parascandola, Historical Consultant,
Rockville, MD
On December 28, 1908, eighteen men met in the
pharmacology lecture room of the Johns Hopkins University
Medical School to establish the American Society for
Pharmacology and Experimental Therapeutics (ASPET). In
2008 ASPET celebrates its Centennial, presenting an appropriate
occasion for a look back at its history.
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Women
in ASPET: A Centennial Perspective
The Pharmacologist,
49: 124-137 (2007)Marlene L. Cohen, Holly L. Brevig, Christine K. Carrico, Lynn
Wecker
As the centennial approaches,
the Women’s Committee of ASPET was inspired to document,
recognize and commemorate the contributions of women to the
Society. This retrospective analysis provides a review of the
role women played in the leadership, growth and accomplishments
of ASPET since its formation in 1908. The information gathered
was highly dependent on records from ASPET as documented in
editions of The Pharmacologist,
a documentary of the
first 60 years of ASPET (Chen, 1969),
the assistance of the
ASPET Executive Office, information readily available on the
internet, and our collective recollection of events and
situations. We hope that this information is both informative
and useful as we move into ASPET's next century.
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Centennial
Perspective: Peter B. Dews and Pharmacological Studies
on
Behavior
Journal
of Pharmacology and Experimental Therapeutics,
326: 683 (2008)
James E. Barrett and
Jack Bergman
The publication by Peter
B. Dews of a series of five articles in this
journal entitled "Studies on Behavior", beginning in
1955 and ending in 1959, were contributions of
extraordinary significance in laying a foundation
for the emergence of the discipline of behavioral
pharmacology. The series of articles were
rigorous in their approach, dramatic in terms of the
results, and provocative in their implications.
Published at the near half-century mark of the
founding of the American Society for
Pharmacological and Experimental Therapeutics, it is
appropriate to now provide a Centennial
Perspective on the impact of these studies over
the 50 years following their publication and to
comment on the way in which they helped to influence the
directions in which this discipline has evolved.
 Humanized
Mouse Lines and Their Application for Prediction of Human
Drug Metabolism and Toxicological Risk Assessment
Journal of
Pharmacology and Experimental Therapeutics,
327: 288 (2008)
Frank J. Gonzalez and Connie
Cheung
Cytochrome P450s (P450s)
are important enzymes involved in the metabolism
of xenobiotics, particularly clinically used drugs,
and are also responsible for metabolic activation of
chemical carcinogens and toxins. Many xenobiotics
can activate nuclear receptors that in turn
induce the expression of genes encoding
xenobiotic metabolizing enzymes and drug transporters.
Marked species differences in the expression and
regulation of cytochromes P450 and xenobiotic
nuclear receptors exist. Thus obtaining reliable
rodent models to accurately reflect human drug and
carcinogen metabolism is severely limited. Humanized
transgenic mice were developed in an effort to
create more reliable in vivo systems to study and
predict human responses to xenobiotics. Human
P450s or human xenobiotic-activated nuclear receptors
were introduced directly or replaced the corresponding
mouse gene, thus creating "humanized" transgenic
mice. Mice expressing human CYP1A1/CYP1A2,
CYP2E1, CYP2D6, CYP3A4, CY3A7, PXR, PPAR
were generated and characterized. These humanized
mouse models offers a broad utility in the
evaluation and prediction of toxicological risk
that may aid in the development of safer drugs.
Guidelines for preparing a Centennial
Perspective (pdf) |