2003
DOI: 10.1016/s0006-8993(03)03087-7
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Expression of neuropeptide Y and cholecystokinin in the rat brain by chronic mild stress

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Cited by 74 publications
(49 citation statements)
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References 38 publications
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“…In addition to the neural effects, the stressed animals showed a net weight loss during the course of the CUS, consistent with other studies of the effects of chronic stress (Kim et al, 2003;Lin et al, 2005;Larsen et al, 2010), whereas the control animals continued to gain weight during the 2 weeks, the animals that underwent CUS did not. Moreover, while corticosterone levels increased in the stressed animals following 2 weeks of CUS, consistent with prior studies of the effects of chronic stress (Hawley et al, 2010), the increase fell just short of statistical significance.…”
Section: Stress-induced Body Weight Loss and Corticosterone Changessupporting
confidence: 90%
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“…In addition to the neural effects, the stressed animals showed a net weight loss during the course of the CUS, consistent with other studies of the effects of chronic stress (Kim et al, 2003;Lin et al, 2005;Larsen et al, 2010), whereas the control animals continued to gain weight during the 2 weeks, the animals that underwent CUS did not. Moreover, while corticosterone levels increased in the stressed animals following 2 weeks of CUS, consistent with prior studies of the effects of chronic stress (Hawley et al, 2010), the increase fell just short of statistical significance.…”
Section: Stress-induced Body Weight Loss and Corticosterone Changessupporting
confidence: 90%
“…This chronic stress model has been shown to produce typical signs of chronic stress exposure, such as elevated corticosterone (Hawley et al, 2010), cardiovascular responses (Hawley et al, 2010), decreased or slowed weight gain (Kim et al, 2003;Lin et al, 2005;Larsen et al, 2010), and decreased neurogenesis (Liu et al, 2007). The CUS paradigm used in the present study was adapted from previously described protocols (Matthews et al, 1995;Alfarez et al, 2003;Gouirand and Matuszewich, 2005;Hawley et al, 2010), and expanded to include more ethologically relevant stressors encountered by an animal in daily life, such as predator odors, sounds, and simulated noninvasive insect-like ''bites'' (Hawley et al, 2010).…”
Section: Chronic Unpredictable Stress (Cus)mentioning
confidence: 99%
“…The reason for this difference is not clear. However, it was reported that NPY immunoreactivity was found mainly in cell bodies of the hypothalamic areas including the ARC and NPY-immunoreactive fibers can be seen in the periventricular hypothalamic nucleus, paraventricular thalamic nucleus, or the PVN, a major site of NPY release (51). Our results suggest that CS may inhibit NPY release or transport in the PVN, rather than synthesis in the ARC even though treatment with CS tended to reduce the expression of NPY in the ARC.…”
Section: Discussionmentioning
confidence: 46%
“…The application of OBX as well as social isolation might promote anterograde transport of CART from the PVN and ARC neuronal cell bodies to the CeA and that the elevation of CART in the CeA might be the key factor in the regulation of depression-like behavior. This concept is supported by the circumstantial evidences such as (1) demonstrated role of PVN and ARC neurons in depression (Baker et al, 1996;Makino et al, 2000;Kim et al, 2003;Sergeyev et al, 2005), (2) occurrence of neuronal connectivity from the PVN and ARC to the amygdala (Eskay et al, 1979;O'Donohue et al, 1979;Cone, 2005), (3) the recognition of amygdala as a site for processing of the depression-related information (Aggleton, 1993;Song et al, 1996;Huang and Lin, 2006;Dannlowski et al, 2008), (4) increase in the CART content in the CeA of rat and its importance in ethanol withdrawal-induced anxiety-like behavior (Dandekar et al, 2008a), (5) our observation that direct injection of CART into the CeA resulted in antidepressant-like effect in the normal rat, and (f) that the depression-like conditions in the socially isolated and OBX animals were reversed by intra-CeA CART treatment. Moreover, the possibility of upregulation of CART expression locally in the CeA following social isolation and OBX may not be ruled out.…”
Section: Effect Of Obx and Social Isolation On Cart-immunoreactivitymentioning
confidence: 70%
“…Moreover, following social isolation and OBX, endogenous CART system was investigated in the paraventricular nucleus (PVN), periventricular area (PeA), arcuate nucleus (ARC), perifornical nucleus (PeF), CeA, prefrontal cortex (PFC), Edinger-Westphal nucleus (EW), and locus coeruleus (LC) using immunocytochemistry coupled with morphometric analysis. These neuroanatomical areas were chosen for this investigation because of abundance of CART (Koylu et al, , 1998Vrang, 2006), and some of them (PVN, ARC, CeA, PFC, and LC) are reported to be involved in the processing of depressionrelated signals (Baker et al, 1996;Song et al, 1996;Makino et al, 2000;Kim et al, 2003;Stone et al, 2007;Dannlowski et al, 2008;Orsetti et al, 2008). Furthermore, this work provided a unique opportunity to compare the CART immunocytochemical profile in the brain of rats subjected to social isolation and OBX, the two different models for generating depression, and to identify common features, if any.…”
Section: Introductionmentioning
confidence: 99%