Oné R. Pagán

Dr. Oné R. Pagán

orcid

Research Focus & Metrics

Academic Career Length

33Years (1994-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
1 October 2006 in Neuroscience Letters
Verified
Journal Article
Closed access
OPOné R. Pagán
Oné R. Pagán
ARAmanda L. Rowlands
Amanda L. Rowlands
KUKimberly R. Urban
Kimberly R. Urban

24 November 1998 in Proceedings of the National Academy of Sciences
Verified
Journal Article
Open access
PDF file
Henning UlrichHenning Ulrich
Henning Ulrich
JIJoseph E. Ippolito
Joseph E. Ippolito
OPOné R. Pagán
Oné R. Pagán
VEVesna A. Eterovic
Vesna A. Eterovic
RHRichard M. Hann
Richard M. Hann
GHGeorge P. Hess
George P. Hess
The nicotinic acetylcholine receptor (AChR) controls signal transmission between cells in the nervous system. Abused drugs such as cocaine inhibit this receptor. Transient kinetic investigations indicate that inhibitors decrease the channel-opening equilibrium constant [Hess, G. P. & Grewer, C. (1998) Methods Enzymol. 291, 443–473]. Can compounds be found that compete with inhibitors for their binding site but do not change the channel-opening equilibrium? The systematic evolution of RNA ligands by exponential enrichment methodology and the AChR in Torpedo californica electroplax membranes were used to find RNAs that can displace inhibitors from the receptor. The selection of RNA ligands was carried out in two consecutive steps: ( i ) a gel-shift selection of high-affinity ligands bound to the AChR in the electroplax membrane, and ( ii ) subsequent use of nitrocellulose filters to which both the membrane-bound receptor and RNAs bind strongly, but from which the desired RNA can be displaced from the receptor by a high-affinity AChR inhibitor, phencyclidine. After nine selection rounds, two classes of RNA molecules that bind to the AChR with nanomolar affinities were isolated and sequenced. Both classes of RNA molecules are displaced by phencyclidine and cocaine from their binding site on the AChR. Class I molecules are potent inhibitors of AChR activity in BC 3 H1 muscle cells, as determined by using the whole-cell current-recording technique. Class II molecules, although competing with AChR inhibitors, do not affect receptor activity in this assay; such compounds or derivatives may be useful for alleviating the toxicity experienced by millions of addicts.

1 January 2017 in The International Journal of Developmental Biology
Verified
Journal Article
Closed access
OPOné R. Pagán
Oné R. Pagán
Although planarians are established model organisms in developmental biology and regeneration studies, in the last forty years or so, they have caught the attention of pharmacologists, especially to study the pharmacology of drugs of abuse. This review covers the following topics: some fundamentals of the history of animal models and planarians in biomedical research; an abbreviated story of systematic pharmacology research using planarians as a model organism; an example of how planarians are contributing to the search for compounds against acute cocaine toxicity; an analysis of the number of papers on planarians and pharmacological topics from 1900-2016; some perspectives on pharmacology in developmental and regeneration studies, arguing in favor of the planarian model as a leading subject for this interdisciplinary area of research, and finally some concluding thoughts.

22 April 2019 in Philosophical Transactions of the Royal Society B: Biological Sciences
Verified
Journal Article
Open access
OPOné R. Pagán
Oné R. Pagán
One of the most important aspects of the scientific endeavour is the definition of specific concepts as precisely as possible. However, it is also important not to lose sight of two facts: (i) we divide the study of nature into manageable parts in order to better understand it owing to our limited cognitive capacities and (ii) definitions are inherently arbitrary and heavily influenced by cultural norms, language, the current political climate, and even personal preferences, among many other factors. As a consequence of these facts, clear-cut definitions, despite their evident importance, are oftentimes quite difficult to formulate. One of the most illustrative examples about the difficulty of articulating precise scientific definitions is trying to define the concept of a brain. Even though the current thinking about the brain is beginning to take into account a variety of organisms, a vertebrocentric bias still tends to dominate the scientific discourse about this concept. Here I will briefly explore the evolution of our ‘thoughts about the brain’, highlighting the difficulty of constructing a universally (or even a generally) accepted formal definition of it and using planarians as one of the earliest examples of organisms proposed to possess a ‘traditional’, vertebrate-style brain. I also suggest that the time is right to attempt to expand our view of what a brain is, going beyond exclusively structural and taxa-specific criteria. Thus, I propose a classification that could represent a starting point in an effort to expand our current definitions of the brain, hopefully to help initiate conversations leading to changes of perspective on how we think about this concept. This article is part of the theme issue ‘Liquid brains, solid brains: How distributed cognitive architectures process information’.

1 November 1994 in Biochemistry
Verified
Journal Article
Closed access
RHRichard M. Hann
Richard M. Hann
OPOné R. Pagán
Oné R. Pagán
VEVesna A. Eterovic
Vesna A. Eterovic

1 August 2009 in European Journal of Pharmacology
Verified
Journal Article
Closed access
OPOné R. Pagán
Oné R. Pagán
ARAmanda L. Rowlands
Amanda L. Rowlands
AFAngela L. Fattore
Angela L. Fattore
TCTamara Coudron
Tamara Coudron
KUKimberly R. Urban
Kimberly R. Urban
VEVesna A. Eterović
Vesna A. Eterović