The Effects of Intra-Cerebral Neuropeptide Y Infusion into the Ventral Hippocampus on Anxiety-Like Behaviour in the Elevated Plus-Maze

Author(s):  
Geoffrey Harrison

Neuropeptide Y (NPY) is one of the most prominent and evolutionarily conserved peptides in the mammalian nervous system. The hippocampus, which contains high densities of NPY producing cells and receptors, is considered a primary structure in the neuroanatomical circuitry of anxiety. Although once considered a homogenous structure, the ventral aspect of the hippocampus is now considered to play a more explicit role in anxiety regulation. To date there is no direct evidence implicating ventral hippocampal NPY in anxiety modulation. By contrasting the defensive behaviours of rats (N=24) in the elevated plus-maze (EPM) model of animal anxiety following intra-cerebral infusions of either experimental NPY (n=12), or saline (n=12), I expect that NPY infusions into the ventral hippocampus will cause marked reductions in anxiety-like behaviour. Specifically, NPY infusions at that site will increase the proportion of entries into, and time spent in, the open arm sections of the EPM, as well as decrease secondary defensive behaviours such as stretch-attend and flatback postures, head-dipping, and sniffing, while in protected portions (walled arms) of the EPM.

2008 ◽  
Vol 1 (1) ◽  
pp. 87-95 ◽  
Author(s):  
Graziela Scarpelli ◽  
Sergio Henrique Alves ◽  
J. Landeira-Fernandez ◽  
Antonio Pedro de Mello Cruz

Author(s):  
Karina Santos Gomes ◽  
Cristiane Álvares Garcia ◽  
Cleopatra da Silva Planeta ◽  
Ricardo Luiz Nunes-de-Souza

2011 ◽  
Vol 7 (4) ◽  
pp. 401-407 ◽  
Author(s):  
Yong Sup Hwang ◽  
Insop Shim ◽  
Jin Woo Chang

Object Hydrocephalus is a pathological enlargement of the ventricles of the brain, which can result from various diseases of the central nervous system. Patients with hydrocephalus frequently show motor abnormalities, such as abnormal gait and posture, as well as intellectual and emotional impairment. The present study was designed to investigate anxiety responses in rats with kaolin-induced hydrocephalus. Methods A total of 26 Sprague-Dawley rats were used for this study. Hydrocephalus was induced in 14 Sprague-Dawley rats by injecting 0.1 ml of 20% kaolin solution into the cisterna magna; 12 rats were administered the same volume of saline in the same fashion and served as controls. Seven of the rats that were injected with kaolin and 6 of the rats injected with saline were killed 3 days after injection (Group 1); the remaining rats were killed 4 weeks after injection (Group 2) to evaluate effects related to acute and chronic hydrocephalus. The rats were tested in an elevated plus maze after induction of hydrocephalus by kaolin injection. After the animals were killed, brain sections were immunostained for cholecystokinin and neuropeptide Y. In addition, tyrosine hydroxlyase immunoreactivity in the ventral tegmental area was evaluated by immunohistological staining. Results The rats with acute hydrocephalus showed decreased entry into and spent less time in the open arms of the elevated plus maze as compared with the control rats. The hydrocephalic rats had significantly more cholecystokinin-immunoreactive neurons and fewer neuropeptide Y–immunoreactive neurons in their brains. In addition, hydrocephalus progress in this model was positively correlated with the anxiety response. The numbers of tyrosine hydroxlyase–immunoreactive neurons were decreased significantly in the hydrocephalic rats as compared with the control rats. Conclusions These results suggest that the rat model of hydrocephalus is characterized by increased anxiety response and is associated with the functional impairment of the central dopamine system.


Author(s):  
Mohammad Sahraei ◽  
Hedayat Sahraei ◽  
Masoomeh Rahimi ◽  
Maryam Khosravi ◽  
Mahin Ganjkhani ◽  
...  

Abstract Objectives The effects of intra-ventral hippocampal memantine administration in male NMRI stressed mice were studied. Methods Two stainless steel gauge 23 guide cannulas were placed in the middle part of the mice ventral hippocampus using stereotaxic coordination. Seven days later, the animals were undergone to the stress protocol as follows: They experience four consecutive electro-foot shock stress sessions lasting for 10 min. Five or 30 min before each stress session, the animals received intra-ventral hippocampal (0.1, 1 and, 5 µg/mouse) or intraperitoneal (1, 5, and 10 mg/kg) memantine respectively. Eight days after stress termination, the animals were tested either for the maintenance of either anxiety (elevated plus maze) or depression (forced swimming test). Results Animals show anxiety eight days after stress termination. Intra-ventral hippocampal infusion of memantine (5 µg/mouse) 5 min before stress inhibited the anxiety-like behaviors. However, other doses of the drug exacerbate the stress effect. The drug, when injected peripherally exacerbated the stress effect in all doses. The drug by itself had no effect. In addition, animals also show depression nine days after stress termination and memantine (0.1, 1, and 5 µg/mouse) reduced the stress effect. The drug (0.1 µg/mouse) by itself induced depression in the animals. However, the drug when injected peripherally reduced the stress effect in all doses. Conclusions It could be concluded that NMDA glutamate receptors in the ventral hippocampus may play a pivotal role in the mediation of maintenance of anxiety and depression induced by stress in the mice.


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