This document summarizes various mechanisms of transport across cell membranes. It discusses passive transport mechanisms like diffusion and facilitated diffusion via transport proteins. Active transport mechanisms powered by ATP hydrolysis are also described, including primary active transport directly powered by ATP and secondary active transport using ion gradients. Specific transport proteins for ions like sodium, potassium, and water are detailed. The document also covers transport of larger molecules via endocytosis and exocytosis, and defines different types of endocytosis.
This study investigated the efficacy of diazepam (DZP) and phenobarbital (PB) in terminating convulsive status epilepticus (CSE) in a mouse model of glucose transporter type 1 deficiency (G1D) syndrome. The researchers found that G1D mice were more susceptible to CSE induced by pilocarpine and less responsive to DZP and PB treatment compared to wild-type mice. Specifically, early treatment with DZP or PB stopped CSE in fewer G1D mice, and late treatment was ineffective. This suggests that drugs used to treat CSE, which inhibit glucose transporter function, may negatively impact outcomes for G1D patients experiencing CSE by exacerbating metabolic
Sodium glucose co transporter( SGLT2) Inhibitors Philip Vaidyan
This document discusses sodium-glucose co-transporter 2 (SGLT2) inhibitors, a new class of drugs for treating type 2 diabetes. SGLT2 inhibitors work by blocking glucose reabsorption in the kidney, increasing urinary glucose excretion in a glucose-dependent manner. Three SGLT2 inhibitors have been approved by the FDA - canagliflozin, dapagliflozin, and empagliflozin. SGLT2 inhibitors offer advantages over other anti-diabetic drugs in that they are non-insulin dependent and can be used throughout the course of diabetes. However, long-term safety studies are still needed to fully assess their risk-benefit profile.
Membranes contain lipids and cholesterol that allow for lateral movement and flexibility. Membrane proteins such as G-protein coupled receptors and transporters control the flow of substances across membranes. G-protein receptors undergo conformational changes upon binding extracellular stimuli, activating intracellular G-proteins and downstream responses. Transporters use passive, active primary and secondary mechanisms to move molecules like glucose and ions across membranes according to concentration gradients.
This document provides an overview of cell membranes and transport systems. It begins by defining the cell membrane and outlining its key functions, including maintaining cell integrity, selective permeability, and transport. It then describes the fluid mosaic model of the cell membrane's structure, which is composed of a phospholipid bilayer with embedded and peripheral proteins. Various types of membrane proteins and their functions are also discussed. The document focuses on different mechanisms of transport across the membrane, including simple diffusion, facilitated diffusion, active transport (primary and secondary), ion channels, and transporter proteins. Specific transport proteins like glucose transporters and ion pumps/channels are highlighted as examples.
Passive transporters like glucose transporter 2 and aquaporins are transmembrane proteins that catalyze the passive movement of molecules like glucose and water across cell membranes. Glucose transporter 2 enables passive glucose movement between the liver and blood while aquaporins regulate water flow by forming pores that selectively conduct water molecules into and out of cells.
Glucose is the main carbohydrate in blood, circulating at 65-110 mg/100 ml. It is an important fuel for muscles. Glucose enters muscles via GLUT4 glucose transporters. There are several glucose transporters with different properties - GLUT1 transports glucose in most cells, GLUT2 in liver and pancreas, GLUT3 in neurons and testes, and GLUT4 in muscles and fat which is activated by insulin. Insulin promotes glucose uptake in muscles by recruiting more GLUT4 transporters to the membrane from intracellular storage vesicles.
The document discusses insulin, its actions, receptors, and regulation. It states that insulin's main sites of action are the liver, muscle, and adipose tissue. Insulin stimulates glycogenesis, lipogenesis, and protein synthesis while inhibiting glycogenolysis, lipolysis, and protein breakdown. Insulin receptors are present on most cells, with high concentrations in the liver, muscle, and fat tissue. GLUT4 is the glucose transporter stimulated by insulin in muscle and fat tissue to increase glucose uptake.
This document summarizes various mechanisms of transport across cell membranes. It discusses passive transport mechanisms like diffusion and facilitated diffusion via transport proteins. Active transport mechanisms powered by ATP hydrolysis are also described, including primary active transport directly powered by ATP and secondary active transport using ion gradients. Specific transport proteins for ions like sodium, potassium, and water are detailed. The document also covers transport of larger molecules via endocytosis and exocytosis, and defines different types of endocytosis.
This study investigated the efficacy of diazepam (DZP) and phenobarbital (PB) in terminating convulsive status epilepticus (CSE) in a mouse model of glucose transporter type 1 deficiency (G1D) syndrome. The researchers found that G1D mice were more susceptible to CSE induced by pilocarpine and less responsive to DZP and PB treatment compared to wild-type mice. Specifically, early treatment with DZP or PB stopped CSE in fewer G1D mice, and late treatment was ineffective. This suggests that drugs used to treat CSE, which inhibit glucose transporter function, may negatively impact outcomes for G1D patients experiencing CSE by exacerbating metabolic
Sodium glucose co transporter( SGLT2) Inhibitors Philip Vaidyan
This document discusses sodium-glucose co-transporter 2 (SGLT2) inhibitors, a new class of drugs for treating type 2 diabetes. SGLT2 inhibitors work by blocking glucose reabsorption in the kidney, increasing urinary glucose excretion in a glucose-dependent manner. Three SGLT2 inhibitors have been approved by the FDA - canagliflozin, dapagliflozin, and empagliflozin. SGLT2 inhibitors offer advantages over other anti-diabetic drugs in that they are non-insulin dependent and can be used throughout the course of diabetes. However, long-term safety studies are still needed to fully assess their risk-benefit profile.
Membranes contain lipids and cholesterol that allow for lateral movement and flexibility. Membrane proteins such as G-protein coupled receptors and transporters control the flow of substances across membranes. G-protein receptors undergo conformational changes upon binding extracellular stimuli, activating intracellular G-proteins and downstream responses. Transporters use passive, active primary and secondary mechanisms to move molecules like glucose and ions across membranes according to concentration gradients.
This document provides an overview of cell membranes and transport systems. It begins by defining the cell membrane and outlining its key functions, including maintaining cell integrity, selective permeability, and transport. It then describes the fluid mosaic model of the cell membrane's structure, which is composed of a phospholipid bilayer with embedded and peripheral proteins. Various types of membrane proteins and their functions are also discussed. The document focuses on different mechanisms of transport across the membrane, including simple diffusion, facilitated diffusion, active transport (primary and secondary), ion channels, and transporter proteins. Specific transport proteins like glucose transporters and ion pumps/channels are highlighted as examples.
Passive transporters like glucose transporter 2 and aquaporins are transmembrane proteins that catalyze the passive movement of molecules like glucose and water across cell membranes. Glucose transporter 2 enables passive glucose movement between the liver and blood while aquaporins regulate water flow by forming pores that selectively conduct water molecules into and out of cells.
Glucose is the main carbohydrate in blood, circulating at 65-110 mg/100 ml. It is an important fuel for muscles. Glucose enters muscles via GLUT4 glucose transporters. There are several glucose transporters with different properties - GLUT1 transports glucose in most cells, GLUT2 in liver and pancreas, GLUT3 in neurons and testes, and GLUT4 in muscles and fat which is activated by insulin. Insulin promotes glucose uptake in muscles by recruiting more GLUT4 transporters to the membrane from intracellular storage vesicles.
The document discusses insulin, its actions, receptors, and regulation. It states that insulin's main sites of action are the liver, muscle, and adipose tissue. Insulin stimulates glycogenesis, lipogenesis, and protein synthesis while inhibiting glycogenolysis, lipolysis, and protein breakdown. Insulin receptors are present on most cells, with high concentrations in the liver, muscle, and fat tissue. GLUT4 is the glucose transporter stimulated by insulin in muscle and fat tissue to increase glucose uptake.
SGLT2 Inhibitors (Gliflozins): A New Class of Drugs to treat Type 2 Diabetes:Naina Mohamed, PhD
Sodium-Glucose Linked Transporter 2 (SGLT2) inhibitors such as Dapagliflozin (Farxiga), Canagliflozin (Invokana) and Empagliflozin (Jardiance) are a new class of oral drugs available to treat type 2 diabetes mellitus (Type 2 DM).
This document discusses various mechanisms of transport in animal physiology, including:
1) Passive transport mechanisms like simple diffusion and facilitated diffusion, as well as active transport mechanisms.
2) The concepts of equilibrium, passive transport which moves with equilibrium, and active transport which moves against equilibrium.
3) Specific passive transport mechanisms like simple diffusion, facilitated diffusion through ion channels, and the factors that determine permeability.
4) How concentration gradients, electrical gradients, and electrochemical equilibrium interact to drive ion transport across membranes.
Active transport moves materials against a concentration or electrochemical gradient and requires energy in the form of ATP. There are two main types: primary active transport which directly utilizes ATP hydrolysis to transport ions via pumps like the Na-K ATPase pump, and secondary active transport which utilizes the gradient established by primary transport to move another substance like symporters and antiporters. Primary transporters include P-type ATPases, V-type ATPases, and F-type ATPases which transport ions like calcium, protons, and help generate mitochondrial membrane potential. Secondary transporters couple the movement of one solute to the gradient of another like the Na-glucose symporter or the Na-Ca exchanger. Active transport is
Carrier mediated drug transport involves drug molecules binding to carrier proteins in cell membranes to be shuttled across. There are two main types - active transport, which uses energy like ATP hydrolysis, and includes primary active transporters like ABC transporters and P-type ATPases like Na+/K+ ATPase; and secondary active transport which uses the gradient of one solute to transport another, like symporters and antiporters. Drugs can also be transported within cells via vesicular transport into intracellular vesicles for release. Key transporters involved in intestinal drug absorption include amino acid, peptide, glucose and bile acid transporters as well as P-glycoprotein efflux pumps.
This document summarizes different types of transport mechanisms in animal cells. It describes passive transport mechanisms like facilitated diffusion that move solutes down their electrochemical gradient. It also describes active transport mechanisms that use energy (ATP) to move solutes against their gradient, including primary active transport via ATPases and secondary active transport using solute gradients. It discusses the coupling of solute transport and defines terms like cotransport and countertransport. Finally, it covers colligative properties of solutions like osmotic pressure and freezing point depression that depend on the number of dissolved particles.
There are 13 glucose transporter proteins (GLUTs) that transport glucose across cell membranes. They are divided into 3 classes. Class I includes GLUT1-4, the most well studied of which are GLUT1, GLUT2, GLUT3 and GLUT4. GLUT1 transports glucose across the blood-brain barrier. GLUT2 acts as a bidirectional transporter in the liver and pancreas. GLUT3 transports glucose into neurons. GLUT4 is the insulin-regulated transporter that transports glucose into muscle and fat cells for storage. Defects in these transporters can lead to diseases like diabetes.
Glucose transport into cells is mediated by glucose transporter (GLUT) proteins. [1] There are five main GLUT transporters that are involved in glucose transport and each has a distinct tissue distribution and function. [2] GLUT transporters use a flip-flop mechanism to transport glucose across the cell membrane according to the concentration gradient. [3] Insulin regulates glucose transport by stimulating the translocation of GLUT4 and GLUT1 transporters from intracellular vesicles to the cell membrane, increasing the influx of glucose into cells.
This document provides information about the digestion and absorption of carbohydrates and their clinical significance. It discusses how carbohydrates are digested by amylases in the mouth, stomach, and small intestine. Disaccharides are further broken down by disaccharidases in the small intestine. The monosaccharides glucose, fructose, and galactose are then absorbed into the bloodstream, primarily through sodium-dependent and sodium-independent glucose transporters. Clinical conditions like lactose intolerance result from deficiencies in disaccharidases like lactase. Overall, the document outlines the multi-step process of carbohydrate digestion and absorption and its implications for health.
PPT on Direct Seeded Rice presented at the three-day 'Training and Validation Workshop on Modules of Climate Smart Agriculture (CSA) Technologies in South Asia' workshop on April 22, 2024.
JAMES WEBB STUDY THE MASSIVE BLACK HOLE SEEDSSérgio Sacani
The pathway(s) to seeding the massive black holes (MBHs) that exist at the heart of galaxies in the present and distant Universe remains an unsolved problem. Here we categorise, describe and quantitatively discuss the formation pathways of both light and heavy seeds. We emphasise that the most recent computational models suggest that rather than a bimodal-like mass spectrum between light and heavy seeds with light at one end and heavy at the other that instead a continuum exists. Light seeds being more ubiquitous and the heavier seeds becoming less and less abundant due the rarer environmental conditions required for their formation. We therefore examine the different mechanisms that give rise to different seed mass spectrums. We show how and why the mechanisms that produce the heaviest seeds are also among the rarest events in the Universe and are hence extremely unlikely to be the seeds for the vast majority of the MBH population. We quantify, within the limits of the current large uncertainties in the seeding processes, the expected number densities of the seed mass spectrum. We argue that light seeds must be at least 103 to 105 times more numerous than heavy seeds to explain the MBH population as a whole. Based on our current understanding of the seed population this makes heavy seeds (Mseed > 103 M⊙) a significantly more likely pathway given that heavy seeds have an abundance pattern than is close to and likely in excess of 10−4 compared to light seeds. Finally, we examine the current state-of-the-art in numerical calculations and recent observations and plot a path forward for near-future advances in both domains.
BIRDS DIVERSITY OF SOOTEA BISWANATH ASSAM.ppt.pptxgoluk9330
Ahota Beel, nestled in Sootea Biswanath Assam , is celebrated for its extraordinary diversity of bird species. This wetland sanctuary supports a myriad of avian residents and migrants alike. Visitors can admire the elegant flights of migratory species such as the Northern Pintail and Eurasian Wigeon, alongside resident birds including the Asian Openbill and Pheasant-tailed Jacana. With its tranquil scenery and varied habitats, Ahota Beel offers a perfect haven for birdwatchers to appreciate and study the vibrant birdlife that thrives in this natural refuge.
PPT on Sustainable Land Management presented at the three-day 'Training and Validation Workshop on Modules of Climate Smart Agriculture (CSA) Technologies in South Asia' workshop on April 22, 2024.
(June 12, 2024) Webinar: Development of PET theranostics targeting the molecu...Scintica Instrumentation
Targeting Hsp90 and its pathogen Orthologs with Tethered Inhibitors as a Diagnostic and Therapeutic Strategy for cancer and infectious diseases with Dr. Timothy Haystead.
Signatures of wave erosion in Titan’s coastsSérgio Sacani
The shorelines of Titan’s hydrocarbon seas trace flooded erosional landforms such as river valleys; however, it isunclear whether coastal erosion has subsequently altered these shorelines. Spacecraft observations and theo-retical models suggest that wind may cause waves to form on Titan’s seas, potentially driving coastal erosion,but the observational evidence of waves is indirect, and the processes affecting shoreline evolution on Titanremain unknown. No widely accepted framework exists for using shoreline morphology to quantitatively dis-cern coastal erosion mechanisms, even on Earth, where the dominant mechanisms are known. We combinelandscape evolution models with measurements of shoreline shape on Earth to characterize how differentcoastal erosion mechanisms affect shoreline morphology. Applying this framework to Titan, we find that theshorelines of Titan’s seas are most consistent with flooded landscapes that subsequently have been eroded bywaves, rather than a uniform erosional process or no coastal erosion, particularly if wave growth saturates atfetch lengths of tens of kilometers.
SGLT2 Inhibitors (Gliflozins): A New Class of Drugs to treat Type 2 Diabetes:Naina Mohamed, PhD
Sodium-Glucose Linked Transporter 2 (SGLT2) inhibitors such as Dapagliflozin (Farxiga), Canagliflozin (Invokana) and Empagliflozin (Jardiance) are a new class of oral drugs available to treat type 2 diabetes mellitus (Type 2 DM).
This document discusses various mechanisms of transport in animal physiology, including:
1) Passive transport mechanisms like simple diffusion and facilitated diffusion, as well as active transport mechanisms.
2) The concepts of equilibrium, passive transport which moves with equilibrium, and active transport which moves against equilibrium.
3) Specific passive transport mechanisms like simple diffusion, facilitated diffusion through ion channels, and the factors that determine permeability.
4) How concentration gradients, electrical gradients, and electrochemical equilibrium interact to drive ion transport across membranes.
Active transport moves materials against a concentration or electrochemical gradient and requires energy in the form of ATP. There are two main types: primary active transport which directly utilizes ATP hydrolysis to transport ions via pumps like the Na-K ATPase pump, and secondary active transport which utilizes the gradient established by primary transport to move another substance like symporters and antiporters. Primary transporters include P-type ATPases, V-type ATPases, and F-type ATPases which transport ions like calcium, protons, and help generate mitochondrial membrane potential. Secondary transporters couple the movement of one solute to the gradient of another like the Na-glucose symporter or the Na-Ca exchanger. Active transport is
Carrier mediated drug transport involves drug molecules binding to carrier proteins in cell membranes to be shuttled across. There are two main types - active transport, which uses energy like ATP hydrolysis, and includes primary active transporters like ABC transporters and P-type ATPases like Na+/K+ ATPase; and secondary active transport which uses the gradient of one solute to transport another, like symporters and antiporters. Drugs can also be transported within cells via vesicular transport into intracellular vesicles for release. Key transporters involved in intestinal drug absorption include amino acid, peptide, glucose and bile acid transporters as well as P-glycoprotein efflux pumps.
This document summarizes different types of transport mechanisms in animal cells. It describes passive transport mechanisms like facilitated diffusion that move solutes down their electrochemical gradient. It also describes active transport mechanisms that use energy (ATP) to move solutes against their gradient, including primary active transport via ATPases and secondary active transport using solute gradients. It discusses the coupling of solute transport and defines terms like cotransport and countertransport. Finally, it covers colligative properties of solutions like osmotic pressure and freezing point depression that depend on the number of dissolved particles.
There are 13 glucose transporter proteins (GLUTs) that transport glucose across cell membranes. They are divided into 3 classes. Class I includes GLUT1-4, the most well studied of which are GLUT1, GLUT2, GLUT3 and GLUT4. GLUT1 transports glucose across the blood-brain barrier. GLUT2 acts as a bidirectional transporter in the liver and pancreas. GLUT3 transports glucose into neurons. GLUT4 is the insulin-regulated transporter that transports glucose into muscle and fat cells for storage. Defects in these transporters can lead to diseases like diabetes.
Glucose transport into cells is mediated by glucose transporter (GLUT) proteins. [1] There are five main GLUT transporters that are involved in glucose transport and each has a distinct tissue distribution and function. [2] GLUT transporters use a flip-flop mechanism to transport glucose across the cell membrane according to the concentration gradient. [3] Insulin regulates glucose transport by stimulating the translocation of GLUT4 and GLUT1 transporters from intracellular vesicles to the cell membrane, increasing the influx of glucose into cells.
This document provides information about the digestion and absorption of carbohydrates and their clinical significance. It discusses how carbohydrates are digested by amylases in the mouth, stomach, and small intestine. Disaccharides are further broken down by disaccharidases in the small intestine. The monosaccharides glucose, fructose, and galactose are then absorbed into the bloodstream, primarily through sodium-dependent and sodium-independent glucose transporters. Clinical conditions like lactose intolerance result from deficiencies in disaccharidases like lactase. Overall, the document outlines the multi-step process of carbohydrate digestion and absorption and its implications for health.
PPT on Direct Seeded Rice presented at the three-day 'Training and Validation Workshop on Modules of Climate Smart Agriculture (CSA) Technologies in South Asia' workshop on April 22, 2024.
JAMES WEBB STUDY THE MASSIVE BLACK HOLE SEEDSSérgio Sacani
The pathway(s) to seeding the massive black holes (MBHs) that exist at the heart of galaxies in the present and distant Universe remains an unsolved problem. Here we categorise, describe and quantitatively discuss the formation pathways of both light and heavy seeds. We emphasise that the most recent computational models suggest that rather than a bimodal-like mass spectrum between light and heavy seeds with light at one end and heavy at the other that instead a continuum exists. Light seeds being more ubiquitous and the heavier seeds becoming less and less abundant due the rarer environmental conditions required for their formation. We therefore examine the different mechanisms that give rise to different seed mass spectrums. We show how and why the mechanisms that produce the heaviest seeds are also among the rarest events in the Universe and are hence extremely unlikely to be the seeds for the vast majority of the MBH population. We quantify, within the limits of the current large uncertainties in the seeding processes, the expected number densities of the seed mass spectrum. We argue that light seeds must be at least 103 to 105 times more numerous than heavy seeds to explain the MBH population as a whole. Based on our current understanding of the seed population this makes heavy seeds (Mseed > 103 M⊙) a significantly more likely pathway given that heavy seeds have an abundance pattern than is close to and likely in excess of 10−4 compared to light seeds. Finally, we examine the current state-of-the-art in numerical calculations and recent observations and plot a path forward for near-future advances in both domains.
BIRDS DIVERSITY OF SOOTEA BISWANATH ASSAM.ppt.pptxgoluk9330
Ahota Beel, nestled in Sootea Biswanath Assam , is celebrated for its extraordinary diversity of bird species. This wetland sanctuary supports a myriad of avian residents and migrants alike. Visitors can admire the elegant flights of migratory species such as the Northern Pintail and Eurasian Wigeon, alongside resident birds including the Asian Openbill and Pheasant-tailed Jacana. With its tranquil scenery and varied habitats, Ahota Beel offers a perfect haven for birdwatchers to appreciate and study the vibrant birdlife that thrives in this natural refuge.
PPT on Sustainable Land Management presented at the three-day 'Training and Validation Workshop on Modules of Climate Smart Agriculture (CSA) Technologies in South Asia' workshop on April 22, 2024.
(June 12, 2024) Webinar: Development of PET theranostics targeting the molecu...Scintica Instrumentation
Targeting Hsp90 and its pathogen Orthologs with Tethered Inhibitors as a Diagnostic and Therapeutic Strategy for cancer and infectious diseases with Dr. Timothy Haystead.
Signatures of wave erosion in Titan’s coastsSérgio Sacani
The shorelines of Titan’s hydrocarbon seas trace flooded erosional landforms such as river valleys; however, it isunclear whether coastal erosion has subsequently altered these shorelines. Spacecraft observations and theo-retical models suggest that wind may cause waves to form on Titan’s seas, potentially driving coastal erosion,but the observational evidence of waves is indirect, and the processes affecting shoreline evolution on Titanremain unknown. No widely accepted framework exists for using shoreline morphology to quantitatively dis-cern coastal erosion mechanisms, even on Earth, where the dominant mechanisms are known. We combinelandscape evolution models with measurements of shoreline shape on Earth to characterize how differentcoastal erosion mechanisms affect shoreline morphology. Applying this framework to Titan, we find that theshorelines of Titan’s seas are most consistent with flooded landscapes that subsequently have been eroded bywaves, rather than a uniform erosional process or no coastal erosion, particularly if wave growth saturates atfetch lengths of tens of kilometers.
Candidate young stellar objects in the S-cluster: Kinematic analysis of a sub...Sérgio Sacani
Context. The observation of several L-band emission sources in the S cluster has led to a rich discussion of their nature. However, a definitive answer to the classification of the dusty objects requires an explanation for the detection of compact Doppler-shifted Brγ emission. The ionized hydrogen in combination with the observation of mid-infrared L-band continuum emission suggests that most of these sources are embedded in a dusty envelope. These embedded sources are part of the S-cluster, and their relationship to the S-stars is still under debate. To date, the question of the origin of these two populations has been vague, although all explanations favor migration processes for the individual cluster members. Aims. This work revisits the S-cluster and its dusty members orbiting the supermassive black hole SgrA* on bound Keplerian orbits from a kinematic perspective. The aim is to explore the Keplerian parameters for patterns that might imply a nonrandom distribution of the sample. Additionally, various analytical aspects are considered to address the nature of the dusty sources. Methods. Based on the photometric analysis, we estimated the individual H−K and K−L colors for the source sample and compared the results to known cluster members. The classification revealed a noticeable contrast between the S-stars and the dusty sources. To fit the flux-density distribution, we utilized the radiative transfer code HYPERION and implemented a young stellar object Class I model. We obtained the position angle from the Keplerian fit results; additionally, we analyzed the distribution of the inclinations and the longitudes of the ascending node. Results. The colors of the dusty sources suggest a stellar nature consistent with the spectral energy distribution in the near and midinfrared domains. Furthermore, the evaporation timescales of dusty and gaseous clumps in the vicinity of SgrA* are much shorter ( 2yr) than the epochs covered by the observations (≈15yr). In addition to the strong evidence for the stellar classification of the D-sources, we also find a clear disk-like pattern following the arrangements of S-stars proposed in the literature. Furthermore, we find a global intrinsic inclination for all dusty sources of 60 ± 20◦, implying a common formation process. Conclusions. The pattern of the dusty sources manifested in the distribution of the position angles, inclinations, and longitudes of the ascending node strongly suggests two different scenarios: the main-sequence stars and the dusty stellar S-cluster sources share a common formation history or migrated with a similar formation channel in the vicinity of SgrA*. Alternatively, the gravitational influence of SgrA* in combination with a massive perturber, such as a putative intermediate mass black hole in the IRS 13 cluster, forces the dusty objects and S-stars to follow a particular orbital arrangement. Key words. stars: black holes– stars: formation– Galaxy: center– galaxies: star formation
Candidate young stellar objects in the S-cluster: Kinematic analysis of a sub...
Types of glucose transporter
1. Types of Glucose Transporter
1. GLUT1
Present in all human tissue, numbers of the carrier protein molecule GLUT-1 are more numerous
in red blood vessels, in the protective membrane of the blood vessels in the brain and in fetal
tissues. GLUT-1 has a strong affinity for glucose molecules, and ensures that both the brain and
red blood cells receive appropriate levels of glucose. GLUT-1 is also able to transport galactose,
but is unable to transport fructose.
2. GLUT-2
GLUT-2 has a lower affinity for glucose than GLUT-1. It is present throughout all bodily tissues,
with the major expression sites being the liver, kidney, pancreas and small intestine. GLUT-2 is
capable of transporting glucose, fructose and galactose. GLUT-2 is most active as a glucose
transporter when high levels of glucose are present, such as after food.
3. GLUT-3
The major expression sites of GLUT-3 are the brain, placenta and testes. GLUT-3 has a high
affinity for glucose, and is also able to transport galactose, but is unable to carry fructose.
GLUT-3 is the primary glucose carrier for neurons or nerve cells.
4. GLUT-4
GLUT-4 is an insulin responsive glucose transporter that has a high affinity for glucose. GLUT-4
only carries glucose. The major expression sites are the cardiac muscle, the skeletal system and
adipocyte cells. Adipocyte cells are fat cells specializing in storing energy as fats. GLUT-4
transports glucose molecules into adipocytes. Adipocyte cells and the skeletal system both
require insulin as well as a glucose transporter protein to absorb glucose molecules from the
bloodstream. Insulin is released from the pancreas which then attaches to receptors on the
adipocyte and skeletal cell membranes. As GLUT-4 is an insulin responsive protein, it is alerted
to the presence of the insulin bound to the receptors on the cell membrane. The GLUT-4
molecule is then able to transport the glucose molecule across the cell membrane and into the
cell.
5. SGLUT-1
SGLUT-1 is a cotransporter molecule, with primary expression sites in the intestinal mucosa and
kidneys. The intestinal mucosa is the lining of the large and small intestine which absorbs
nutrients. Cotransporter molecules usually carry two different sorts of molecules. SGLUT-1
carries one molecule of either glucose or galactose as well as two sodium ions. SGLUT-1 is
unable to carry fructose.
References
Types of Glucose Transporters By Katy Willis, eHow Contributor [online].
available at http://www.ehow.com/list_6869400_types-glucose-transporters.html
AccessedOctober2,2013