1996
DOI: 10.1016/0168-0102(95)01015-7
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Involvement of nitric oxide in acute spinal cord injury: an immunocytochemical study using light and electron microscopy in the rat

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Cited by 125 publications
(119 citation statements)
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“…49 Nitric oxide synthetase (NOS) is upregulated following injury and NOS antiserum has been shown to have a protective eect. 39 In the early phase following injury, changes in neurotransmitters such as substance P and acetyl choline have been identi®ed and the expression of trophic factors such as B-50 (GAP-43) studied. 50,51 The early gene c-jun is transiently expressed and c-fos continuously in the experimental model.…”
Section: ± 48mentioning
confidence: 99%
See 1 more Smart Citation
“…49 Nitric oxide synthetase (NOS) is upregulated following injury and NOS antiserum has been shown to have a protective eect. 39 In the early phase following injury, changes in neurotransmitters such as substance P and acetyl choline have been identi®ed and the expression of trophic factors such as B-50 (GAP-43) studied. 50,51 The early gene c-jun is transiently expressed and c-fos continuously in the experimental model.…”
Section: ± 48mentioning
confidence: 99%
“…These generate an in¯ammatory response which is responsible for some of the continuing damage. 36,39,40 Polymorphs and monocytes migrate through the vessel walls into the damaged parenchyma. Here the monocytes are converted to macrophages which present antigens' to lymphocytes which then continue the assault.…”
Section: Restorative Neurologymentioning
confidence: 99%
“…Use of antibodies therapy to neutralize the endogenous effects of their antigens in various disease conditions has been emphasized recently (Sharma et al, 1995d(Sharma et al, , 1996aFaden, 1990). The antibodies are considered much more effective in neutralizing the effects of the neurochemicals in vivo than pharmacological blockade of their receptors (Faden, 1990;Sharma et al, 1995a).…”
Section: Neurotrophins Influence Bcsnb Function To Enhance Neuroregenmentioning
confidence: 98%
“…Thus, one possibility is that spinal injury might trigger NO production in EMNs and could regulate their regenerative responses to such injuries. In the mammalian spinal cord, peripheral nerve injury or spinal cord lesions either up-or down-regulate NOS, depending on the nature of the lesion and the age of the animal [Wu, 1993;Yu, 1994;Zdanski et al, 1994;Sharma et al, 1996;Gordh et al, 1998;Callsen-Cencic et al, 1999;Suzuki et al, 2001]. Depending on the concentration, cell types, and conditions, NO can have either neuroprotective or neurotoxic/ neurodegenerative effects [Krönke et al, 1997;Pantazis et al, 1998;Thippeswamy et al, 2001].…”
Section: Discussionmentioning
confidence: 99%