Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UNIPROT:P20366 (substance P)
 21,176 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The anatomical and biochemical features of primary sensory afferents and the peptidergic innervation of cremaster motoneuron efferents in the genitofemoral (Gf) nerve were analyzed in the rat using immunohistochemical, histochemical, retrograde tracing and lesion methods. Afferent fibers in the Gf nerve were shown to originate from neurons in L1 and L2 dorsal root ganglia (DRG) and to project to L1 to T12.5 in the spinal cord. Some of the DRG neurons giving rise to these fibers contained substance P (SP) or the enzyme fluoride-resistant acid phosphatase but none appeared to contain somatostatin. The dermatome area of the Gf nerve, as determined by plasma extravasation methods, was located in the rostral scrotal and adjacent abdominal region. Identification of cremaster motoneurons by retrograde labelling from the Gf nerve revealed these neurons to be located in the L1 to L2 spinal cord segment, to have prominent rostrocaudally oriented dendritic aborizations and to receive a rich innervation by fibers containing SP, thyrotropin-releasing hormone (TRH) or met-enkephalin (met-Enk). Lesion studies indicated the SP-and met-Enk-containing fibers to be supplied by local intraspinal systems and the TRH-containing fibers by supraspinal systems. In female rats, motoneurons corresponding to the male version of the cremaster motoneuronal pool were less developed and received far fewer peptidergic connections than that observed in males. The multiple neural systems innervating cremaster motoneurons together with sensory afferents in the Gf and other scrotal nerves are suggested to be involved in the contribution of cremaster muscles to thermoregulation of the scrotum.
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PMID:Neural relations of cremaster motoneurons, spinal cord systems and the genitofemoral nerve in the rat. 393 95

Electrical stimulation of the distal stump of cut peripheral nerves is a commonly accepted way to evoke neurogenic inflammation. Nevertheless, the modulatory effect of biogenic amines and vasoactive peptides released from efferent fibres can be excluded only if the dorsal roots are stimulated. The present study was focussed to investigate plasma extravasation in the appropriate skin and mucosal areas as well as in the genito-urinary organs in response to antidromic stimulation of the lumbar and sacral dorsal roots of the rat. Plasma extravasation was detected by quantitative measurement of the accumulated Evans Blue tracer in tissue pieces. Two unilateral posterior roots were stimulated simultaneously (20 V, 0.5 ms, 5 Hz, 5 min) in each anaesthetized rat. Intensive blueing response occurred in the following tissues: plantar glabrous skin, L4-L5 (L6); dorsum of the hindpaw and ankle joint, L2-L4; ventral surface of the thigh, L2-L4 (L1); abdominal skin, L1-L4; caudal nipples, L1-L2; root of the tail, S1 orifice of the vagina, S1 (L6); vagina, L2-L3, L5-S1; cervix and corpus uteri, L2-L3, L5-S1; lower two-thirds of the uterine horns, L1-L3; urinary bladder, L1-L3, L6-S1; rectum, L5-S1; scrotum (dorsal surface and lower pole), L6-S1; scrotum (ventral surface), L3-L5. No significant dye accumulation was observed in the muscles, testicles, vas deferens and prostate. Plasma extravasation caused by antidromic activation of the dorsal roots was absent or highly reduced after systemic capsaicin pretreatment of the rats. Neurogenic inflammation evoked by antidromic stimulation of the dorsal roots makes this method suitable for mapping the organs where capsaicin-sensitive sensory nerve endings exert their "efferent functions". This first functional description of segmental innervation of capsaicin-sensitive afferent fibres is in agreement with retrograde tracing studies and immunohistochemical localization of substance P in the dorsal root ganglia and peripheral tissues.
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PMID:Plasma extravasation in the skin and pelvic organs evoked by antidromic stimulation of the lumbosacral dorsal roots of the rat. 747 70

In rats treated with Evans blue (i.v.), electrical stimulation of the lumbar spinal nerves produced an extravasation zone in the skin. Stimulation of L1 produced extravasation in the lower abdomen; that of L2, in the cranial region of the hindlimb; that of L3, in the ventral region of the hindlimb and the medial paw; that of L4, in the lateral region of the hindlimb and the middle paw; that of L5, in the caudal region of the hindlimb and the lateral paw; and that of L6, in the caudal region of the hindlimb and the scrotum. Since the substance P antagonist FK224 inhibited the extravasation caused by stimulation of the sciatic nerve, the extravasation zones appeared to be related to antidromic activation of afferent C-fibers. Thus, a dermatome of afferent C-fibers was revealed in rats.
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PMID:Dermatome mapping in the rat hindlimb by electrical stimulation of the spinal nerves. 751 69

1 The dartos is a thin sheet of smooth muscle closely associated with the skin of the scrotum. Although known to play an important role in scrotal thermoregulation, there has been no detailed study into the pharmacology, or thermosensitivity, of the dartos from any species. Here, we investigate these two parameters in the isolated dartos muscle from rat. 2 Field stimulation of the rat dartos caused contractions that were abolished by tetrodotoxin, phentolamine and guanethidine, but unaffected by atropine or L-N(G)-nitroarginine. Exogenous noradrenaline also produced contractions blocked by both phentolamine and prazosin. In muscles with raised tone and negated sympathetic function, field stimulation failed to elicit relaxation. The dartos muscle did not contract in response to carbachol, nicotine, histamine, 5-hydroxytryptamine (all up to 100 micro M) or substance P (up to 1 micro M). 3 Contractile responses to field stimulation and noradrenaline were much greater at 30 degrees C compared with 40 degrees C; indeed, contractions to 1 micro M noradrenaline at 30 degrees C were relaxed by around 80% on heating to 40 degrees C. Similar heat-induced relaxations were observed during contractions to both U46619 (100 nM) and high K (70 mM). 4 In contrast, contractile responses to the myosin phosphatase inhibitor calyculin-A (1 micro M), either in the presence or absence of external calcium, were resistant to relaxation by heating. In calcium-free medium at 30 degrees C, U46619 continued to produce contractions that were again relaxed by 80% on heating to 40 degrees C. However, in the presence of calyculin-A, this heat-induced relaxation was greatly reduced. 5 Thus, the rat dartos muscle receives a functional sympathetic innervation and contracts to noradrenaline via alpha-adrenoceptors. There is no functional inhibitory innervation. Experiments with calyculin-A suggest that myosin phosphatase is a major contributor to the marked thermosensitivity of the dartos muscle.
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PMID:Pharmacology and thermosensitivity of the dartos muscle isolated from rat scrotum. 1216 53