Literature DB >> 3525370

Calcitonin gene-related peptide in the hepatic and splanchnic vascular systems of the rat.

Y Sasaki, N Hayashi, A Kasahara, H Matsuda, H Fusamoto, N Sato, C J Hillyard, S Girgis, I MacIntyre, P C Emson.   

Abstract

The distribution and origin of calcitonin gene-related peptide immunoreactive structures in hepatic and splanchnic vasculature of the rat were investigated by the immunofluorescent technique. Calcitonin gene-related peptide immunoreactive fibers were dissociated from compact thick calcitonin gene-related peptide immunoreactive fiber bundles located around the hepatic and splanchnic vasculature, and reached the tunica adventitia of the vasculature. Some fibers penetrated further into the tunica media of the vasculature. In the tunica adventitia of the vasculature, calcitonin gene-related peptide immunoreactive fibers formed a fine meshwork which could be traced to the branches and arterioles. In the liver, calcitonin gene-related peptide immunoreactive innervation extended from porta hepatis to portal triads, running with branches of the hepatic artery and portal vein. Some calcitonin gene-related peptide immunoreactive fibers separated from thinner calcitonin gene-related peptide immunoreactive fiber bundles in portal triads and coursed into the immediately adjacent parenchyma. In the dorsal spinal ganglia (T8-10, L1), calcitonin gene-related peptide immunoreactive cells accounted for about 60% of the total number of ganglion cells. Bilateral vagotomy just below the diaphragm or bilateral transection of the greater splanchnic nerve resulted in a marked decrease of the number of calcitonin gene-related peptide immunoreactive fibers in the vasculature, whereas a combined operation was followed by the complete depletion of calcitonin gene-related peptide immunoreactive fibers. These results indicate that calcitonin gene-related peptide immunoreactive innervation in hepatic and splanchnic vasculature may have a dual origin. In conclusion, the widespread distribution of calcitonin gene-related peptide immunoreactive fibers in the hepatic and splanchnic vasculature suggest that calcitonin gene-related peptide innervation may be involved in sensory transmission.

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Year:  1986        PMID: 3525370     DOI: 10.1002/hep.1840060423

Source DB:  PubMed          Journal:  Hepatology        ISSN: 0270-9139            Impact factor:   17.425


  9 in total

1.  Cross-reactivity of amylin with calcitonin-gene-related peptide binding sites in rat liver and skeletal muscle membranes.

Authors:  A Chantry; B Leighton; A J Day
Journal:  Biochem J       Date:  1991-07-01       Impact factor: 3.857

2.  Abstracts of selected papers: 29th annual meeting of the Japanese Society of Gastroenterology. Kofu, Japan, November 5-7, 1987.

Authors: 
Journal:  Gastroenterol Jpn       Date:  1988-08

3.  Splanchnic and cerebral vasodilatory effects of calcitonin gene-related peptide I in humans.

Authors:  M W Mulholland; M S Sarpa; J Delvalle; L M Messina
Journal:  Ann Surg       Date:  1991-10       Impact factor: 12.969

4.  The effect of CGRP-induced hypotension on organ blood flow during halothane anesthesia in dogs: a comparison with trimetaphan.

Authors:  Shohei Takeda; Teruaki Tomaru; Yutaka Inada
Journal:  J Anesth       Date:  1997-09       Impact factor: 2.078

5.  Endothelium-dependent and endothelium-independent vasodilatation of the hepatic artery of the rabbit.

Authors:  A L Brizzolara; G Burnstock
Journal:  Br J Pharmacol       Date:  1991-05       Impact factor: 8.739

6.  Human alpha-calcitonin gene-related peptide (CGRP) is a potent vasodilator in human mesenteric vasculature.

Authors:  I Marshall; S J Al-Kazwini; J J Holman; R K Craig
Journal:  Br J Clin Pharmacol       Date:  1988-12       Impact factor: 4.335

Review 7.  Peptides in the mammalian cardiovascular system.

Authors:  J Wharton; S Gulbenkian
Journal:  Experientia       Date:  1987-07-15

8.  Postnatal development of the rat portal vein: correlation with occurrence of peptidergic innervation.

Authors:  M Ody; A Thiévent; M Millet; J L Connat
Journal:  Cell Tissue Res       Date:  1993-05       Impact factor: 5.249

9.  Hepatocyte membrane potential regulates serum insulin and insulin sensitivity by altering hepatic GABA release.

Authors:  Caroline E Geisler; Susma Ghimire; Chelsea Hepler; Kendra E Miller; Stephanie M Bruggink; Kyle P Kentch; Mark R Higgins; Christopher T Banek; Jun Yoshino; Samuel Klein; Benjamin J Renquist
Journal:  Cell Rep       Date:  2021-06-29       Impact factor: 9.423

  9 in total

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