Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
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Query: UNIPROT:P61278 (
somatostatin
)
22,083
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
The distribution and the frequency of occurrence of nine types of gut endocrine cells were revealed using immunohistochemical methods in eight portions from the gastrointestinal tract of the chicken (
Gallus gallus
var domestica). In the proventriculus,
somatostatin
- and gastrin-releasing polypeptide (GRP)-immunoreactive cells were commonly found. Serotonin-, pancreatic glucagon-, and enteroglucagon-immunoreactive cells were uncommon. Avian pancreatic polypeptide (APP)-immunoreactive cells were rare. In the gizzard, numerous GRP-, and a small number of
somatostatin
-immunoreactive cells were observed. The pyloric region was characterized by the presence of abundant gastrin-,
somatostatin
-, and neurotensin-immunoreactive cells. Numerous serotonin-immunoreactive cells were detected in all portions of the intestine. Moderate numbers of neurotensin-immunoreactive cells were detected in all portions of the intestine except for the cecum. A few gastrin- and
somatostatin
-immunoreactive cells were detected in the duodenum and jejunum. A small number of pancreatic glucagon-immunoreactive cells were detected in the jejunum and ileum. Enteroglucagon-immunoreactive cells were detected in the small intestine in increasing numbers forwards the ileum. Motilin-immunoreactive cells were rare in the small intestine.
...
PMID:An immunohistochemical study on the distribution of endocrine cells in the chicken gastrointestinal tract. 280 Jun 74
Somatostatin
and its receptors have a critical role in mammalian growth through their control pattern of secretion of growth hormone, but the evolutionary history of
somatostatin
and
somatostatin
receptors are ill defined. We used comparative whole genome analysis of Danio rerio, Carassius auratus, Xenopus tropicalis,
Gallus gallus
, Monodelphis domestica, Homo sapiens, Sus scrofa, Bos taurus, Mus musculus, Rattus norvegicus, Canis lupus familiaris, Ovis aries, Equus caballus, Pan troglodytes and Macaca mulatto to identify
somatostatin
and
somatostatin
receptors in each species. To date, we have identified a minimum of two genes of
somatostatin
and five somatostatin receptor genes in mammalian species with variable forms. We established a clear evolutionary history of the
somatostatin
system and traced the origin of the
somatostatin
system to 395 million years ago (MYA), identifying critical steps in their evolution.
...
PMID:Evolutionary history of the somatostatin and somatostatin receptors. 1941 43
The present study was designed to investigate the ontogeny and tissue distribution of
somatostatin
and its five receptor subtypes (SSTR1-5) mRNA expression in embryonic chicken (
Gallus gallus
). Brain, gonads (male), intestine, kidney, liver, muscle, stomach and yolk sac membrane (YSM) of chicken embryos on the embryonic (E) ages of 10, 16 and 21days (right before hatch) were investigated. Bisulfite sequencing PCR (BSP) was performed to determine the methylation status of the promoter region of all the six genes in the liver.
Somatostatin
(
SST
) was predominately expressed in intestine, brain and gonads (male) with different ontogenic patterns. The highest expression in intestine was detected at E10. There was ontogenic shift from intestine to brain as development progressed. Expression pattern of SSTRs in brain, intestine and kidney was similar to human embryonic expression. In liver, the ontogenic expression pattern of
SST
and its receptors was associated to methylation status of the respective promoters. Methylation of site Sp1 determines expression level of
SST
, SSTR1, SSTR2 and SSTR3 while site a is important in governing the expression of SSTR4 and SSTR5. The results show that ontogenic expression profile of chicken
SST
and SSTRs is time and tissue specific.
...
PMID:Ontogeny of mRNA expression of somatostatin and its receptors in chicken embryos in association with methylation status of their promoters. 2372 27