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Substance P
LE WE PMID CA
Substance P3324Substanz P

12 Hydroxyeicosatetraenoic acid

12 s HPETE

AMG9810 ttTRPV1

BQ123 ttEndothelinETA

BQ788 ttEndothelinETB

Calcitonin gene related peptide

CGRP8 37 ttCGRP

Endothelin

Endotoxin

Endovanilloid

ERSNA efferent renal sympathetic nervous activity

Gastroesophageal reflux disease

H89 ttPKA

Hematopoietic growth factors (Pharmacology)

Inflammation (BASKET)

Ischemia reperfusion

Ischemic preconditioning

Kidney (Nerves afferent)

Kidney (Pressure natriuresis)

L733060 ttNeurokinin1

Mechanotransduction

N oleoyldopamine

PAF

Pain (Neurophysiology)

PAR2

Pelvis (Kidney)

PKC epsilon V1 2 ttPKCepsilon

RAAS (Renin)

Receptor (Neurokinin1)

Resiniferatoxin ttTRPV1

RP67580 ttNeurokinin1

SLIGRL ttPAR2

Sodium (Salt)

Substance P

Tetrabutylammonium tt PotassiumChannels

TRPV1

TRPV4

2001  
1
Substance P: a pioneer amongst neuropeptides.
[11168782] J Intern Med 249(1): 27-40 (2001)
2010  
2
Neurokinin-1 receptor: a new promising target in the treatment of cancer.
[21034671] Discov Med 10(53): 305-13 (2010)
2007  
3
The significance of substance P in physiological and malignant haematopoiesis.
[17172475] J Clin Pathol 60(7): 749-55 (2007)
2008  
4
N-oleoyldopamine, a novel endogenous capsaicin-like lipid, protects the heart against ischemia-reperfusion injury via activation of TRPV1.
[18567714] Am J Physiol Heart Circ Physiol 295(2): H728-35 (2008)
2007  
5
TRPV1 gene knockout impairs preconditioning protection against myocardial injury in isolated perfused hearts in mice.
[17586621] Am J Physiol Heart Circ Physiol 293(3): H1791-8 (2007)
2009  
6
Protease-activated receptor 2-mediated protection of myocardial ischemia-reperfusion injury: role of transient receptor potential vanilloid receptors.
[19812353] Am J Physiol Regul Integr Comp Physiol 297(6): R1681-90 (2009)
2008  
7
TRPV1-mediated protection against endotoxin-induced hypotension and mortality in rats.
[18337316] Am J Physiol Regul Integr Comp Physiol 294(5): R1517-23 (2008)
2008  
8
Transient receptor potential vanilloid type 1 channels act as mechanoreceptors and cause substance P release and sensory activation in rat kidneys.
[18032552] Am J Physiol Renal Physiol 294(2): F316-25 (2008)
2009  
9
Ablation of transient receptor potential vanilloid 1 abolishes endothelin-induced increases in afferent renal nerve activity: mechanisms and functional significance.
[19858408] Hypertension 54(6): 1298-305 (2009)
2010  
10
Viewpoints on Acid-induced inflammatory mediators in esophageal mucosa.
[21103419] J Neurogastroenterol Motil 16(4): 374-88 (2010)
2011  
11
Inhibition of renin release by arachidonic acid metabolites, 12(s)-HPETE and 12-HETE: role of TRPV1 channels.
[21846804] Endocrinology 152(10): 3811-9 (2011)
2010  
12
A role for transient receptor potential vanilloid 4 in tonicity-induced neurogenic inflammation.
[20136846] Br J Pharmacol 159(5): 1161-73 (2010)
2009  
13
Salt intake augments hypotensive effects of transient receptor potential vanilloid 4: functional significance and implication.
[19075100] Hypertension 53(2): 228-35 (2009)
2005  
14
Feed-forward inhibition: a novel cellular mechanism for the analgesic effect of substance P.
[16297242] Mol Pain 1(-): 34 (2005)

Downloaded from http://www.kidney.de - The Database of Free Medical Reviews - The Metatextbook of Medicine - Ossip Groth

All Medline data shown were primarily retrieved from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.


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