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Somatostatin

Somatostatin is a peptide hormone that regulates the endocrine system by inhibiting the release of numerous other hormones, including growth hormone, thyroid-stimulating hormone, and insulin.
It is produced by specialized cells called delta cells, primarily found in the pancreas and gastrointestinal tract.
Somatostatin plays a key role in maintaining homeostasis and suppressing excessive secretion of hormones.
It has a wide range of therapeutic applications, including the treatment of acromegaly, neuroendocrine tumors, and diarrhea.
Researchers can optimize their somatostatin studies with PubCompare.ai, an AI-powered tool that enhances reproducibility and accuracy by locating protocols from literature, preprints, and patents, and providing intelligent comparisons to identify the best protocols and products for their experiments.
This can streamline the research process and deliver more reliable results.

Most cited protocols related to «Somatostatin»

Adult wild-type, male and female transgenic Parvalbumin-IRES-Cre30 (link) (Jax 008069), Parvalbumin-2a-Cre29 (Jax 012358), Tyrosine Hydroxylase-Cre (EMMA 00254), and Somatostatin-Flp C57/BL6 mice were group housed up to four to a cage and kept on a reverse 12 hour light/dark cycle with ad libitum food and water. Experimental protocols were approved by Stanford University IACUC and meet guidelines of the National Institutes of Health guide for the Care and Use of Laboratory Animals.
Publication 2014
Adult Animals, Laboratory Animals, Transgenic Females Food Institutional Animal Care and Use Committees Internal Ribosome Entry Sites Males Mice, Laboratory Parvalbumins Somatostatin Tyrosine 3-Monooxygenase
Rats and mice were maintained on a standard diet and water ad lib. After anesthesia (pentobarbital; 50 mg/kg) liver and kidney were fixed and paraffin-embedded. Cholangiocytes were isolated from control and PCK rats as described(20 (link)) and from liver transplant tissue of healthy human beings and patients with ADPKD (see Supporting Information for details). PAS and OCT were kindly provided by Novartis USA. The protocol was approved by the Mayo IACUC.
Treatment protocol is shown in Fig. 1. Rodents received PAS and OCT for 6 weeks. Drug doses were chosen based on our studies.(7 (link)) Somatostatin analogues were dissolved in sterile water and administered via osmotic mini-pumps (model 2002, Alzet Osmotic Pumps, Cupertino, CA). Pumps were implanted subcutaneously on the animal back under anesthesia with 1.5% isoflurane (Baxter, Deerfield, IL). They were replaced every 2 weeks; at this time OCT and PAS concentrations were adjusted to the animal weight. Cystic and fibrotic areas were analyzed as described in Supporting Information.
See Supporting Information for additional experimental procedures.
Publication 2012
Anesthesia Animals Cyst Diet Fibrosis Homo sapiens Institutional Animal Care and Use Committees Isoflurane Kidney Liver Mice, House Osmosis Paraffin Patients Pentobarbital Pharmaceutical Preparations Polycystic Kidney, Autosomal Dominant Rattus Rodent Somatostatin Sterility, Reproductive Tissue Grafts Treatment Protocols
One of the most important features of an evidence map is the cataloging of the large number and variety of outcomes reported in the published literature. This step typically occurs after data extraction since the scope of an evidence-map database is large. Thus, it is often difficult to pre-define all outcome categories of interest. The research team worked with the stakeholder panel to classify outcomes into clinically and biologically meaningful outcome categories that could be used in evidence-map analyses. The research team recorded outcomes reported in each publication and took the first attempt in identifying clinically and biologically relevant groups. Standardized coding was then developed for each outcome category. Feedback was sought from the stakeholder panel, and the outcome categories and coding were modified based on the final consensus of the stakeholder panel. Table 2 shows the final list of outcomes for each outcome category that are reported in the studies included in the LCS evidence-map database. Specifically, outcomes related to appetite or satiety ratings such as hunger score and desire to eat were often rated by a visual analog scale (VAS) and were classified under the ‘Appetite’ category. Outcomes focused on neurological measurements and sensing signals by the brain were classified under the ‘Energy Sensing’ category. Body weight, body composition and changes in weight-related outcomes were classified under the ‘Body Weight or Composition’ category. The ‘Dietary Intake’ category included outcomes such as energy intake, dietary intake, food intake and carbohydrate intake, and finally the ‘Glycemic’ category included glucose, insulin and gastric hormones. Our stakeholder panel did not identify additional outcomes that were not reported in the literature. Both outcome categories and full outcome lists were included in the evidence-map database, which can be used in future analyses with current or new outcome category coding.

Outcomes of interest by outcome groups in the LCS evidence-map database

Outcome groupsOutcomes of interest
AppetiteAppetite ratings using a visual analog scale (VAS), hunger, desire to eat, fullness, prospective consumption, thirst, motivational and behavioral factors reported through questionnaire
Energy sensing by brainNeurological measurements (fMRI, EEG), sensory rating (sweetness, intensity, pleasantness, sensory specific satiation), taste, perception and preference, taste reaction time
Body weight or body compositionBody weight, body composition, BMI, waist circumferences, weight or BMI changes
Dietary intakeEnergy intake, dietary intake, food intake, carbohydrate intake, sugar intake, salt intake, water intake
GlycemicGlucose, Hemoglobin A1c (HbA1c), insulin concentration, insulin sensitivity, hypoglycemia, glucagon, glucose-dependent insulinotropic peptide (GIP), glucagon-like peptide-1 (GLP-1), peptide tyrosine tyrosine (PYY), cholecystokinin (CCK), enterostatin, ghrelin, leptin, somatostatin, oxyntomodulin
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Publication 2016
Body Composition Brain Carbohydrates Cholecystokinin Eating fMRI Gastric Inhibitory Polypeptide Ghrelin Glucagon Glucagon-Like Peptide 1 Glucose Hemoglobin A, Glycosylated Hormones Hunger Hypoglycemia Insulin Insulin Sensitivity Leptin Motivation Oxyntomodulin procolipase Sodium Chloride, Dietary Somatostatin Stomach Taste Thirst tyrosyltyrosine Visual Analog Pain Scale Waist Circumference

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Publication 2012
Antibodies Antigens, Nuclear Apoptosis Biological Assay Cell Nucleus Cells DAPI Electron Microscopy Equus asinus Fluorescein-5-isothiocyanate Genotype Glucagon Immunofluorescence Immunohistochemistry In Situ Nick-End Labeling Insulin Laser Scanning Microscopy Microscopy, Confocal Molecular Probes Mus Pancreas Pancreatic beta Cells Peroxidase Proteins Somatostatin Student Tissues Transcription Factor
Literature searches were performed by meeting participants to identify new data in English language papers published between January 2014 and October 2019, and indexed in PubMed. Search terms included “acromegaly” and terms associated with each topic, including “biochemical control”, “tumor volume”, “clinical symptoms”, “side effects”, “neurosurgery”, “radiother-apy”, “somatostatin analogue”, “somatostatin receptor ligand”, “pegvisomant”, “morbidity”, “mortality”, “quality of life”,and “guidelines”. After brief plenary overviews on the state of the art for each topic, participants were divided into breakout groups for further analysis of the assigned topics and subsequently reported their conclusions to the whole group.
Consensus recommendations were produced based on speaker presentations, subgroup discussions, and reports. After the meeting, the Scientific Committee graded the evidence supporting the recommendations, and then graded the
consensus recommendations on the basis of the quality of evidence (Table 2). Final graded consensus recommendations were approved by all meeting participants.
Publication 2020
Acromegaly Ligands Neurosurgical Procedures pegvisomant Somatostatin Somatostatin Receptor

Most recents protocols related to «Somatostatin»

If the patient's preoperative total bilirubin was >300 mmol/L, percutaneous transhepatic cholangial drainage (PTCD) should be performed for two weeks to reduce jaundice or preoperative total bilirubin to <51 mmol/L. On the 3rd day after operation, when the flow of nasogastric tube was less than 200 mL/D, nasogastric tube was removed. On the 3rd day after operation, the drainage fluid of abdominal drainage tube was collected, and the concentration of amylase was detected. When the drainage volume was less than 20 mL, drainage tube was removed. On the 5th day after operation, routine computed tomography (CT) scanning was performed on the upper abdomen to understand abdominal abscess and effusion. On the 3rd day after operation, patients began to eat liquid food. All patients were treated with somatostatin analogues.
International Study Group of Pancreatic Surgery (ISGPF) classification was used for the definition of postoperative complications (POPF, delayed gastric emptying, and postpancreatectomy hemorrhage (PPH)) [30 (link)–32 (link)], while POPF grades B and C were regarded as clinically relevant. Postoperative bleeding was defined as a PPH grade B or C according to the ISGPF [32 (link)]. Acute pancreatitis was chemically defined as an elevated serum amylase and/or lipase level (at least three times of the normal level) for at least 3 consecutive days on the 3rd day after operation. Acute pancreatitis was confirmed by CT. The classification of postoperative complications was the Clavien-Dindo classification [33 (link)]. The FRS is a 10-point scale that relies on weighted effect of four variables including gland texture, pathology, duct size, and estimated blood loss [34 (link), 35 (link)]. The weighted aggregate of these risk factors was used to calculate the individual FRS score (0-10) for each patient.
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Publication 2023
Abdomen Abdominal Abscess Abdominal Cavity Amylase Bilirubin Drainage Food Hemorrhage Hyperamylasemia Icterus Lipase Pancreas Pancreatitis, Acute Patients Postoperative Complications Serum Somatostatin Surgery, Day X-Ray Computed Tomography
Experiments were performed on male and female C57/Bl6 mice aged 4–8 weeks. Slc6a4-cre::Rosa-TdTomato (SERT-Cre) and Sst-cre::Rosa-TdTomato transgenic lines were used to fluorescently label DRN 5-HT and somatostatin (SOM) GABA neurons, respectively. Animals were group-housed and kept on a 12:12 hr light/dark cycle with access to food and water ad libitum. All experiments were carried out in accordance with procedures approved by the University of Ottawa Animal Care and Veterinary Services (protocol numbers CMM-164, CMM-176, CMM-1711, CMM-1743, and CMM-2737).
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Publication 2023
Animals Animals, Transgenic Females Food GABAergic Neurons Males Mice, Laboratory Rosa SLC6A4 protein, human Somatostatin tdTomato

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Publication 2023
Abdomen Amylase Antibiotics, Antitubercular Choledochojejunostomy Condoms Drainage Gastrojejunostomy Pancreas Pancreaticoduodenectomy Pancreaticojejunostomy Patients Somatostatin Surgeons Surgical Anastomoses Therapy, Diet
At admission, every patient had a medical interview and underwent a physical examination. Blood samples of all patients were taken after overnight fasting. IGF-1 and GH were measured. According to guidelines, nadir GH in the oral glucose tolerance test was measured in all non-diabetic patients. In patients with diabetes mellitus and in those, who had already been treated with somatostatin analogues, random GH was calculated as an arithmetic mean of five measurements of blood samples obtained every 30 min. MRI scan of the pituitary gland was also performed routinely in all patients with acromegaly unless there were no contraindications. Treatment naïve acromegaly was diagnosed when all of the following criteria were fulfilled:

IGF-1 elevated above the age-adjusted upper norm limit

Lack of suppression of GH below 1 ng/mL in 75 g oral glucose tolerance test (patients without diabetes) or random GH levels above 2.5 ng/mL (patients with diabetes)

A pituitary gland tumour visualised in magnetic resonance imaging (MRI) or computed tomography (CT) (in patients with contraindications for MRI).

Previously treated patients who achieved age-normalisation of IGF-1 and normalisation of GH (GH < 1 ng/mL in 75 g OGTT or random GH < 2.5 ng/mL in diabetic patients) were classified as a stable/controlled group. Acromegaly was considered active/uncontrolled (non-remission group) when IGF-1 and GH were elevated in patients who had already been treated. Patients who could not be classified according to the above-mentioned criteria were excluded from the analysis. Tumour invasiveness was defined as the infiltration of surrounding tissues.
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Publication 2023
Acromegaly BLOOD Diabetes Mellitus IGF1 protein, human Neoplasm Invasiveness Oral Glucose Tolerance Test Patients Physical Examination Pituitary Neoplasms Somatostatin Tissues X-Ray Computed Tomography
Between September 2013 and December 2016, a total of 51 consecutive patients with clinically and functionally confirmed type 2 amiodarone-induced thyrotoxicosis were treated on the clinical bases of the Sechenov University (University Clinical Hospitals № 1 and 2). Among these 51 patients, we enrolled 39 registered in the hospitals mentioned above. The inclusion criteria were the following: (1) history of amiodarone treatment; (2) a serum concentration of amiodarone at 0.5–2.5 mg/mL; (3) decreased levels of thyroid-stimulating hormone (TSH), increased concentration of free thyroxine (T4), free triiodothyronine (T3); (4) an decrease of 99mTc-pertechnetate accumulation and thyroid uptake of less than 1% according to scintigraphy. The remaining 12 patients were excluded from the study according to the exclusion criteria: (1) any proven thyroid disease prior to amiodarone treatment; (2) administration of lithium drugs, glucocorticoids, phenytoin, interferon, iron supplements, estrogens, somatostatin analogs; (3) pregnancy and lactation; (4) severe comorbidities; (5) mental disorders affecting patient compliance. Thirty-nine patients receiving amiodarone treatment for at least six months exhibiting no thyroid pathology were included as a control arm.
Participants have provided written informed consent and all experimental methods were in accordance with the 1975 Declaration of Helsinki. This study was approved by the Review Board of the Sechenov University. All procedures were performed in accordance with the ethical principles for medical research.
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Publication 2023
Amiodarone Breast Feeding Dietary Supplements Estrogens Glucocorticoids Interferons Iron Liothyronine Lithium Mental Disorders Patients Pertechnetate Phenytoin Pregnancy Radionuclide Imaging Serum Somatostatin Thyroid Diseases Thyroid Gland Thyrotoxicosis Thyrotropin Thyroxine

Top products related to «Somatostatin»

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Somatostatin is a synthetic peptide hormone that functions as an inhibitor of various endocrine and exocrine secretions. It is primarily used as a laboratory reagent for research and experimental purposes.
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MAB354 is a laboratory equipment product manufactured by Merck Group. It is designed for use in various scientific research and analytical applications. The core function of MAB354 is to provide a reliable and precise measurement or analysis of samples. Detailed technical specifications and intended use cases are not available in this unbiased and factual presentation.
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DAPI is a fluorescent dye used in microscopy and flow cytometry to stain cell nuclei. It binds strongly to the minor groove of double-stranded DNA, emitting blue fluorescence when excited by ultraviolet light.
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Guinea pig anti-insulin is a laboratory reagent used for the detection and measurement of insulin in biological samples. It is a specific antibody produced in guinea pigs that binds to insulin, allowing for its identification and quantification through various analytical techniques.
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Goat anti-somatostatin is a polyclonal antibody produced in goats and directed against the neuropeptide somatostatin. It is intended for use in research applications involving the detection and quantification of somatostatin in various biological samples.
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Alexa Fluor 488 is a fluorescent dye used in various biotechnological applications. It has an excitation maximum at 495 nm and an emission maximum at 519 nm, producing a green fluorescent signal. Alexa Fluor 488 is known for its brightness, photostability, and pH-insensitivity, making it a popular choice for labeling biomolecules in biological research.
Rat anti-somatostatin is an antibody product used in laboratory research. It is designed to detect and bind to the somatostatin peptide hormone. Somatostatin is involved in the regulation of various physiological processes. The rat anti-somatostatin antibody can be utilized in techniques such as immunoassays to study somatostatin and its functions.
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The A0566 is a lab equipment product from Agilent Technologies. It is designed to perform a core laboratory function. No further details about its intended use or specific capabilities are provided.
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Mouse anti-glucagon is a laboratory reagent used for the detection and quantification of glucagon, a peptide hormone produced by the pancreas that plays a role in regulating blood glucose levels. This product is designed for use in various research and diagnostic applications.

More about "Somatostatin"

Somatostatin, also known as growth hormone-inhibiting hormone (GHIH) or somatotropin release-inhibiting factor (SRIF), is a cyclic peptide hormone that plays a crucial role in regulating the endocrine system.
This versatile molecule is produced by specialized delta cells, predominantly found in the pancreas and gastrointestinal tract.
Somatostatin's primary function is to inhibit the release of various hormones, including growth hormone, thyroid-stimulating hormone, and insulin, thereby maintaining homeostasis and suppressing excessive hormone secretion.
Somatostatin's therapeutic applications are wide-ranging, making it a valuable tool in the treatment of conditions like acromegaly, neuroendocrine tumors, and diarrhea.
Researchers can optimize their somatostatin studies by utilizing PubCompare.ai, an AI-powered tool that enhances the reproducibility and accuracy of their experiments.
PubCompare.ai helps researchers locate relevant protocols from literature, preprints, and patents, and provides intelligent comparisons to identify the best protocols and products for their specific needs.
This streamlined approach can deliver more reliable results and accelerate the research process.
Beyond somatostatin, researchers may also work with related biomolecules such as MAB354, DAPI, A0564, Guinea pig anti-insulin, Goat anti-somatostatin, Alexa Fluor 488, Rat anti-somatostatin, A0566, and Mouse anti-glucagon.
These tools and reagents can be integrated into somatostatin-focused studies to provide a comprehensive understanding of this critical endocrine regulator.
By leveraging the insights and capabilities offered by PubCompare.ai, researchers can unlock new discoveries and advance our knowledge of somatostatin and its role in maintaining physiological balance.