scholarly journals Effect of 6-Hydroxydopamine Treatment in the Area Postrema on Morphine-Induced Emesis in Ferrets

2002 ◽  
Vol 89 (4) ◽  
pp. 422-425 ◽  
Author(s):  
Takashi Yoshikawa ◽  
Naoyuki Yoshida
1988 ◽  
Vol 254 (4) ◽  
pp. R711-R716 ◽  
Author(s):  
T. A. Day ◽  
J. R. Sibbald

Recent studies confirm that the supraoptic nucleus (SON) receives a direct projection from the nucleus of the solitary tract (NTS). We have examined the effect of NTS stimulation on antidromically identified SON neurosecretory cells that were classified as arginine vasopressin (AVP) or oxytocin (OXY) secreting in accord with basal activity patterns and responsiveness to arterial baroreceptor activation. Medial NTS stimulation at the level of the obex or area postrema excited 78% (59 of 76) of putative AVP cells (onset latency 52 +/- 1 ms) but only 20% (3 of 15) of putative OXY cells. Commissural NTS stimulation did not excite AVP cells (n = 13). After complete SON catecholamine afferent disruption, achieved by local injection of 6-hydroxydopamine, AVP cells tested were unresponsive to medial NTS stimulation (12 of 13), although arterial baroreceptor activation inhibited four of four cells. These data indicate that medial NTS stimulation preferentially excites SON AVP cells and that this effect involves an adrenergic input to SON. A direct projection from the A2 catecholamine cell group of the NTS may be involved, although the long latency to excitation and the poor correspondence between effective NTS stimulation sites and the location of the A2 group within NTS raise the possibility that a relay projection, possibly through the A1 catecholamine cell group of the ventrolateral medulla, may be involved.


1976 ◽  
Vol 104 (1) ◽  
pp. 187-192 ◽  
Author(s):  
Peter M. Klara ◽  
Richard M. Kostrezewa ◽  
Kenneth R. Brizzee

Author(s):  
Shams M. Ghoneim ◽  
Frank M. Faraci ◽  
Gary L. Baumbach

The area postrema is a circumventricular organ in the brain stem and is one of the regions in the brain that lacks a fully functional blood-brain barrier. Recently, we found that disruption of the microcirculation during acute hypertension is greater in area postrema than in the adjacent brain stem. In contrast, hyperosmolar disruption of the microcirculation is greater in brain stem. The objective of this study was to compare ultrastructural characteristics of the microcirculation in area postrema and adjacent brain stem.We studied 5 Sprague-Dawley rats. Horseradish peroxidase was injected intravenously and allowed to circulate for 1, 5 or 15 minutes. Following perfusion of the upper body with 2.25% glutaraldehyde in 0.1 M sodium cacodylate, the brain stem was removed, embedded in agar, and chopped into 50-70 μm sections with a TC-Sorvall tissue chopper. Sections of brain stem were incubated for 1 hour in a solution of 3,3' diaminobenzidine tetrahydrochloride (0.05%) in 0.05M Tris buffer with 1% H2O2.


1976 ◽  
Vol 17 (3) ◽  
pp. 419-419 ◽  
Author(s):  
Masayori OZAKI ◽  
Kazunobu SUGAWARA ◽  
Naoko TAKAMI ◽  
Masashi OGAWA ◽  
Masami NIWA

2020 ◽  
Vol 20 (10) ◽  
pp. 1560-1568 ◽  
Author(s):  
Yan-Qiu Wang ◽  
Yi-Bing Chen ◽  
Dong Xu ◽  
Yuan-Lu Cui

Objective: Energy metabolism disorder is one of the causes of Parkinson's disease (PD). Rodents, such as rats and mice are often used to establish animal models of PD. This paper used a bibliometric method to analyze the studies of rat and mouse PD models published between 2009 and 2018 in the Web of Science (WOS) database using CiteSpace V software. In addition, we conducted a literature review on the development status and research hotspots in this field in the past ten years. Methods: The related articles on rat and mouse PD models were retrieved from the WOS database, and an analysis of the keywords in these articles was conducted using CiteSpace V. A timeline graph was developed by the software in order to show the focus of researchers in the PD field. Results : A total of 8,636 articles were obtained. Results of the cluster analysis in the PD field such as neuroinflammation, oxidative stress, and autophagy, contributed to the systematic review about the pathogenesis of PD. At the same time, based on the property of the model drug, this review has summarized and compared different administration techniques and mechanisms of 6-hydroxydopamine (6- OHDA), 1-methyl-4-phenyl-1, 2, 4, 5-tetrahydropyridine (MPTP), paraquat and rotenone. Conclusion: According to the bibliometric analysis, studies on PD were focused on the mechanisms of oxidative stress, neuroinflammation, and autophagy. Activated microglia releases inflammatory cytokines; mitochondrial dysfunction is caused by oxidative damage of mitochondrial protein; abnormal autophagy-lysosome pathway can lead to abnormal protein deposition in dopaminergic neurons. In addition, although many animal models of PD have been established, there are some limitations of such models. Therefore, it is necessary to develop models that accurately mimic human PD.


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