2010
DOI: 10.1016/j.neuroscience.2010.07.047
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Neuropeptide coding of sympathetic preganglionic neurons; focus on adrenally projecting populations

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Cited by 22 publications
(24 citation statements)
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“…In-situ hybridization for custom synthesized and validated prepro-enkephalin (PPE) riboprobe incorporated with digoxigenin (DIG)-11-UTP (Roche Applied Science, Mannheim, Germany) was performed (final concentration 1000 ng/ml) in conjunction with fluorescent immunohistochemical (IHC) detection as described previously (Bowman et al, 2013;Kumar et al, 2010;Parker et al, 2013). No alkaline phosphatase reaction product is seen after hybridization with our PPE mRNA sense probe, or in the absence of antisense DIGriboprobes in rat spinal cord tissue (Kumar et al, 2010;Parker et al, 2013).…”
Section: 7mentioning
confidence: 99%
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“…In-situ hybridization for custom synthesized and validated prepro-enkephalin (PPE) riboprobe incorporated with digoxigenin (DIG)-11-UTP (Roche Applied Science, Mannheim, Germany) was performed (final concentration 1000 ng/ml) in conjunction with fluorescent immunohistochemical (IHC) detection as described previously (Bowman et al, 2013;Kumar et al, 2010;Parker et al, 2013). No alkaline phosphatase reaction product is seen after hybridization with our PPE mRNA sense probe, or in the absence of antisense DIGriboprobes in rat spinal cord tissue (Kumar et al, 2010;Parker et al, 2013).…”
Section: 7mentioning
confidence: 99%
“…No alkaline phosphatase reaction product is seen after hybridization with our PPE mRNA sense probe, or in the absence of antisense DIGriboprobes in rat spinal cord tissue (Kumar et al, 2010;Parker et al, 2013). Table 1 details the antibodies used.…”
Section: 7mentioning
confidence: 99%
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“…(d'Ascanio et al, 2002;Nestler et al, 1999). Polyclonal CTB antiserum was raised in rabbit and conjugated to biotin (Virostat; 7927), No labeling was seen in the brains of rats that were not injected with CTB in the spinal cord (see also Kumar et al, 2010).…”
Section: Antibody Characterization and Titrationmentioning
confidence: 99%
“…In effect, there may be a shift in the balance of PAC 1 , compared with VPAC 1 and VPAC 2 , function. Furthermore, the chemical phenotype of SPN that project to epinephrine-releasing chromaffin cells is different to that of SPN, regulating norepinephrine-releasing chromaffin cells (24). Therefore, the results observed here may be due to partial blockade of PAC 1 receptors by catestatin, with a change in the balance toward excitation of epinephrine-releasing pathways that cause an increase in heart rate, a large decrease in peripheral resistance, and a subsequent fall in blood pressure (14,16).…”
Section: Catestatin Amplifies Responses To Pacap-38mentioning
confidence: 75%