Investigating the Dopaminergic Synapse In Vivo. II. Molecular Imaging Studies in Small Laboratory Animals

2007 ◽  
Vol 18 (6) ◽  
Author(s):  
Susanne Nikolaus ◽  
Rolf Larisch ◽  
Markus Beu ◽  
Christina Antke ◽  
Konstantin Kley ◽  
...  
2007 ◽  
Vol 191 (S51) ◽  
pp. s13-s18 ◽  
Author(s):  
Oliver D. Howes ◽  
Andrew J. Montgomery ◽  
Marie-Claude Asselin ◽  
Robin M. Murray ◽  
Paul M. Grasby ◽  
...  

SummaryThe dopamine hypothesis has been the major pathophysiological theory of psychosis in recent decades. Molecular imaging studies have provided in vivo evidence of increased dopamine synaptic availability and increased presynaptic dopamine synthesis in the striata of people with psychotic illnesses. These studies support the predictions of the dopamine hypothesis, but it remains to be determined whether dopaminergic abnormalities pre-date or are secondary to the development of psychosis. We selectively review the molecular imaging studies of the striatal dopaminergic system in psychosis and link this to models of psychosis and the functional subdivisions of the striatum to make predictions for the dopaminergic system in the prodromal phase of psychosis


2020 ◽  
Author(s):  
Hebaalla Agha ◽  
Christopher R. McCurdy

Molecular imaging studies have paved the road for the development of successful σ1R ligands currently in clinical trials.


2004 ◽  
Vol 96 (6) ◽  
pp. 2109-2114 ◽  
Author(s):  
Sune P. Straszek ◽  
Ole F. Pedersen

The purpose of the study was to measure nasal passageway dimensions in guinea pigs and rats by use of acoustic rhinometry (AR) and by a previously described fluid-displacement method (FDM) (Straszek SP, Taagehoej F, Graff S, and Pedersen OF. J Appl Physiol 95: 635–642, 2003) to investigate the potential of AR in pharmacological research with these animals. We measured the area-distance relationships by AR of nasal cavities postmortem in five guinea pigs (Duncan Hartley, 400 g) and five rats (Wistar, 250 g) by using custom-made equipment scaled for the purpose. Nosepieces were made from plastic pipette tips and either inserted into or glued onto the nostrils. We used liquid perfluorocarbon in the fluid-displacement study, and it was carried out subsequent to the acoustic measurements. We found for guinea pigs that AR measured a mean volume of 98 mm3 (95–100 mm3) (mean and 95% confidence interval) of the first 2 cm of the cavity. FDM measured a mean volume of 146 mm3 (117–175 mm3), meaning that AR only measured 70% (50–90) of the volume by FDM. For rats, the volume from 0 to 2 cm was 58 mm3 (55–61 mm3) by AR and 73 mm3 (60–87 mm3) by FDM, resulting in AR only measuring 83% (66–100%) of volume by FDM (see Table 2 ). We conclude that absolute nasal cavity dimensions are underestimated by AR in guinea pigs and rats. This does not preclude that relative changes may be correctly measured. In vivo trials with AR using rats have not yet been published. The FDM is possibly the most accurate alternative to AR for measurements of the nasal cavity geometry in small laboratory animals, but it can only be used postmortem.


2018 ◽  
Vol 9 (4) ◽  
pp. 105-112 ◽  
Author(s):  
Valeria A. Pechatnikova ◽  
Alexander P. Trashkov ◽  
Maria A. Zelenenko ◽  
Nikolay A. Verlov ◽  
Grigorii A. Chizh ◽  
...  

For a long time non-invasive imaging methods have been inaccessible in preclinical practice; their introduction lately has broadened the boundaries of relevant studies and felicitated new approaches to solving fundamental problems. Up-to-date imaging methods constitute an essential component of preclinical and translational biomedical research allowing quick and non-invasive extended representation of structural organization and functional characteristics of pathological processes in vivo. Methods of radiation diagnosis and nuclear magnetic resonance allow to assess the state of bones, soft tissues, internal organs, blood vessels and peripheral nerve fibers in various animals, not only mammals, but also fish, amphibians, reptiles and insects. Multiparametric studies can uniquely localize any anatomical structure or pathological process. However, not all existing techniques are applicable to various oncological models of small laboratory animals.


Author(s):  
R. S. McCuskey

Most organs in anesthetized small laboratory animals can be studied in vivo by light microscopy of relatively thin (3-5mm), transilluminated areas of the organ. Thicker areas of the organs in these species, as well as thicker organs of larger animals can be examined only by epi-ilumination. However, the resolution obtainable with epi-ilumination usually is inferior to that realized with transillumination. This paper reviews these methods using the liver as an example of the organ of study. A standard compound trinocular microscope is used which is modified for in vivo microscopy and is equipped for both transillumination and epi-illumination. After the animal is anesthetized, the liver is gently exteriorized through a subcostal, abdominal incision and positioned over a window of optical grade mica or glass on a specially designed, heated microscope stage having provisions for draining irrigation fluids. The window overlies a long working distance condenser. The liver is covered by a piece of Saran or Mylar film which holds it in position and limits movements induced by respiration, the heart and the intestines.


2019 ◽  
Vol 3 (4) ◽  
pp. 319-328

Th is review is dedicated to the peculiarities of pathogenesis of the experimental Bolivian hemorrhagic fever (BHF) – the disease, caused by Machupo virus (Arenaviridae family). Th e authors come to the conclusion that for carrying out preclinical researches of the medical means of protection (MMP) in vivo on small laboratory animals it is expedient to use guinea pigs, infected with a strain of Chicava or with a variant of Carvallo strain, adapted for these animals. Th e use of guinea pigs as small laboratory animals when studying pathogenesis of the disease caused by Machupo virus allows to carry out statistically reliable defi nition of quantitative indices of an experimental infection and to select medicines for the fi nal stage of preclinical assessment. As arenaviruses block the process of formation of interferon (IFN) in the infected organism, mice, defective by IFN formation, are the perspective animal models for the study of BHF pathogenesis and may be used for the study of attenuated variants of Machupo virus. Th e Javanese macaques (Macaca fascicularis) are the laboratory animals, modeling the pathogenetic manifestations of BHF in humans. Th ey can be used when carrying out the fi nal stages of preclinical assessment of means of medical protection


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