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.
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Somatostatin
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.
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
Animals, Laboratory
Animals, Transgenic
Females
Food
Institutional Animal Care and Use Committees
Internal Ribosome Entry Sites
Males
Mice, Laboratory
Parvalbumins
Somatostatin
Tyrosine 3-Monooxygenase
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 groups | Outcomes of interest |
---|---|
Appetite | Appetite 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 brain | Neurological measurements (fMRI, EEG), sensory rating (sweetness, intensity, pleasantness, sensory specific satiation), taste, perception and preference, taste reaction time |
Body weight or body composition | Body weight, body composition, BMI, waist circumferences, weight or BMI changes |
Dietary intake | Energy intake, dietary intake, food intake, carbohydrate intake, sugar intake, salt intake, water intake |
Glycemic | Glucose, 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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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
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
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.
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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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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Animals
Animals, Transgenic
Females
Food
GABAergic Neurons
Males
Mice, Laboratory
Rosa
SLC6A4 protein, human
Somatostatin
tdTomato
Protocol full text hidden due to copyright restrictions
Open the protocol to access the free full text link
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).
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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.
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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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»
Sourced in United States, Argentina
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.
Sourced in United States, Switzerland
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.
Sourced in United States, Germany, United Kingdom, Japan, China, Canada, Italy, Australia, France, Switzerland, Spain, Belgium, Denmark, Panama, Poland, Singapore, Austria, Morocco, Netherlands, Sweden, Argentina, India, Finland, Pakistan, Cameroon, New Zealand
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.
Sourced in United States, Denmark, Japan, United Kingdom
The A0564 is a compact and versatile laboratory equipment designed for precise measurement and analysis. It features a range of high-quality sensors and advanced data processing capabilities to support a variety of scientific applications. The core function of the A0564 is to provide accurate and reliable data for research, testing, and quality control purposes.
Sourced in United States, United Kingdom, Denmark, Canada
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.
Sourced in United States
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.
Sourced in United States, United Kingdom, Germany, Japan, France, Italy, Canada, China, Spain, Switzerland, Denmark, Australia, Hungary, Belgium, Ireland, Israel, Netherlands, Moldova, Republic of, India, Austria, Czechia, Poland
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.
Sourced in United States, Denmark
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.
Sourced in United States, Denmark
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.
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.