A phenolphthalein that is used as a diagnostic aid in hepatic function determination.
Liquid substances produced by living organisms to fulfill specific functions or excreted as waste.
A water-soluble radiographic contrast media for cholecystography and intravenous cholangiography.
A bile pigment that is a degradation product of HEME.
Membrane proteins whose primary function is to facilitate the transport of negatively charged molecules (anions) across a biological membrane.
A tricarbocyanine dye that is used diagnostically in liver function tests and to determine blood volume and cardiac output.
Negatively charged atoms, radicals or groups of atoms which travel to the anode or positive pole during electrolysis.
A subclass of ORGANIC ANION TRANSPORTERS that do not rely directly or indirectly upon sodium ion gradients for the transport of organic ions.
An emulsifying agent produced in the LIVER and secreted into the DUODENUM. Its composition includes BILE ACIDS AND SALTS; CHOLESTEROL; and ELECTROLYTES. It aids DIGESTION of fats in the duodenum.
A large lobed glandular organ in the abdomen of vertebrates that is responsible for detoxification, metabolism, synthesis and storage of various substances.
Proteins involved in the transport of organic anions. They play an important role in the elimination of a variety of endogenous substances, xenobiotics and their metabolites from the body.
The movement of materials (including biochemical substances and drugs) through a biological system at the cellular level. The transport can be across cell membranes and epithelial layers. It also can occur within intracellular compartments and extracellular compartments.
Steroid acids and salts. The primary bile acids are derived from cholesterol in the liver and usually conjugated with glycine or taurine. The secondary bile acids are further modified by bacteria in the intestine. They play an important role in the digestion and absorption of fat. They have also been used pharmacologically, especially in the treatment of gallstones.
Transport proteins that carry specific substances in the blood or across cell membranes.
A tripeptide with many roles in cells. It conjugates to drugs to make them more soluble for excretion, is a cofactor for some enzymes, is involved in protein disulfide bond rearrangement and reduces peroxides.
Genetically identical individuals developed from brother and sister matings which have been carried out for twenty or more generations or by parent x offspring matings carried out with certain restrictions. This also includes animals with a long history of closed colony breeding.
The rate dynamics in chemical or physical systems.

Quantitative aspects in the assessment of liver injury. (1/199)

Liver function data are usually difficult to use in their original form when one wishes to compare the hepatotoxic properties of several chemical substances. However, procedures are available for the conversion of liver function data into quantal responses. These permit the elaboration of dose-response lines for the substances in question, the calculation of median effective doses and the statistical analysis of differences in liver-damaging potency. These same procedures can be utilized for estimating the relative hazard involved if one compares the liver-damaging potency to the median effective dose for some other pharmacologie parameter. Alterations in hepatic triglycerides, lipid peroxidation, and the activities of various hepatic enzymes can also be quantitiated in a dose-related manner. This permits the selection of equitoxic doses required for certain comparative studies and the selection of doses in chemical interaction studies. The quantitative problems involved in low-frequency adverse reactions and the difficulty these present in the detection of liver injury in laboratory animals are discussed.  (+info)

Polyspecific substrate uptake by the hepatic organic anion transporter Oatp1 in stably transfected CHO cells. (2/199)

The rat liver organic anion transporting polypeptide (Oatp1) has been extensively characterized mainly in the Xenopus laevis expression system as a polyspecific carrier transporting organic anions (bile salts), neutral compounds, and even organic cations. In this study, we extended this characterization using a mammalian expression system and confirm the basolateral hepatic expression of Oatp1 with a new antibody. Besides sulfobromophthalein [Michaelis-Menten constant (Km) of approximately 3 microM], taurocholate (Km of approximately 32 microM), and estradiol- 17beta-glucuronide (Km of approximately 4 microM), substrates previously shown to be transported by Oatp1 in transfected HeLa cells, we determined the kinetic parameters for cholate (Km of approximately 54 microM), glycocholate (Km of approximately 54 microM), estrone-3-sulfate (Km of approximately 11 microM), CRC-220 (Km of approximately 57 microM), ouabain (Km of approximately 3,000 microM), and ochratoxin A (Km of approximately 29 microM) in stably transfected Chinese hamster ovary (CHO) cells. In addition, three new substrates, taurochenodeoxycholate (Km of approximately 7 microM), tauroursodeoxycholate (Km of approximately 13 microM), and dehydroepiandrosterone sulfate (Km of approximately 5 microM), were also investigated. The results establish the polyspecific nature of Oatp1 in a mammalian expression system and definitely identify conjugated dihydroxy bile salts and steroid conjugates as high-affinity endogenous substrates of Oatp1.  (+info)

Maturational disturbance of chondrocytes in Cbfa1-deficient mice. (3/199)

Cbfa1, a transcription factor that belongs to the runt-domain gene family, plays an essential role in osteogenesis. Cbfa1-deficient mice completely lacked both intramembranous and endochondral ossification, owing to the maturational arrest of osteoblasts, indicating that Cbfa1 has a fundamental role in osteoblast differentiation. However, Cbfa1 was also expressed in chondrocytes, and its expression was increased according to the maturation of chondrocytes. Terminal hypertrophic chondrocytes expressed Cbfa1 extensively. The significant expression of Cbfa1 in hypertrophic chondrocytes was first detected at embryonic day 13.5 (E13.5), and its expression in hypertrophic chondrocytes was most prominent at E14.5-16.5. In Cbfa1-deficient mice, whose entire skeleton was composed of cartilage, the chondrocyte differentiation was disturbed. Calcification of cartilage occurred in the restricted parts of skeletons, including tibia, fibula, radius, and ulna. Type X collagen, BMP6, and Indian hedgehog were expressed in their hypertrophic chondrocytes. However, osteopontin, bone sialoprotein, and collagenase 3 were not expressed at all, indicating that they are directly regulated by Cbfa1 in the terminal hypertrophic chondrocytes. Chondrocyte differentiation was severely disturbed in the rest of the skeleton. The expression of PTH/PTHrP receptor, Indian hedgehog, type X collagen, and BMP6 was not detected in humerus and femur, indicating that chondrocyte differentiation was blocked before prehypertrophic chondrocytes. These findings demonstrate that Cbfa1 is an important factor for chondrocyte differentiation.  (+info)

Primary active transport of organic anions on bile canalicular membrane in humans. (4/199)

Biliary excretion of several anionic compounds was examined by assessing their ATP-dependent uptake in bile canalicular membrane vesicles (CMV) prepared from six human liver samples. 2, 4-Dinitrophenyl-S-glutathione (DNP-SG), leukotriene C4 (LTC4), sulfobromophthalein glutathione (BSP-SG), E3040 glucuronide (E-glu), beta-estradiol 17-(beta-D-glucuronide) (E2-17G), grepafloxacin glucuronide (GPFXG), pravastatin, BQ-123, and methotrexate, which are known to be substrates for the rat canalicular multispecific organic anion transporter, and taurocholic acid (TCA), a substrate for the bile acid transporter, were used as substrates. ATP-dependent and saturable uptake of TCA, DNP-SG, LTC4, E-glu, E2-17G, and GPFXG was observed in all human CMV preparations examined, suggesting that these compounds are excreted in the bile via a primary active transport system in humans. Primary active transport of the other substrates was also seen in some of CMV preparations but was negligible in the others. The ATP-dependent uptake of all the compounds exhibited a large inter-CMV variation, and there was a significant correlation between the uptake of glutathione conjugates (DNP-SG, LTC4, and BSP-SG) and glucuronides (E-glu, E2-17G, and GPFXG). However, there was no significant correlation between TCA and the other organic anions, implying that the transporters for TCA and for organic anions are different also in humans. When the average value for the ATP-dependent uptake by each preparation of human CMVs was compared with that of rat CMVs, the uptake of glutathione conjugates and nonconjugated anions (pravastatin, BQ-123, and methotrexate) in humans was approximately 3- to 76-fold lower than that in rats, whereas the uptake of glucuronides was similar in the two species. Thus there is a species difference in the primary active transport of organic anions across the bile canalicular membrane that is less marked for glucuronides.  (+info)

Uptake of bromosulfophthalein via SO2-4/OH- exchange increases the K+ conductance of rat hepatocytes. (5/199)

In confluent primary cultures of rat hepatocytes, micromolar concentrations of bromosulfophthalein (BSP) lead to a sizeable hyperpolarization of membrane voltage. The effect is a saturable function of BSP concentration yielding an apparent value of 226 micromol/l and a Vmax of -10.3 mV. The BSP-induced membrane hyperpolarization is inhibited by the K+ channel blocker Ba2+, and in cable-analysis and ion-substitution experiments it becomes evident that the effect is due to a significant increase in cell membrane K+ conductance. Voltage changes were attenuated by the simultaneous administration of SO2-4, succinate, and cholate (cis-inhibition) and increased after preincubation with SO2-4 and succinate (trans-stimulation), suggesting that the effect occurs via BSP uptake through the known SO2-4/OH- exchanger. Microfluorometric measurements reveal that BSP-induced activation of K+ conductance is not mediated by changes in cell pH, cell Ca2+, or cell volume. It is concluded that K+ channel activation by BSP (as well as by DIDS and indocyanine green) may reflect a physiological mechanism linking the sinusoidal uptake of certain anions to their electrogenic canalicular secretion.  (+info)

Hepatic uptake of the magnetic resonance imaging contrast agent gadoxetate by the organic anion transporting polypeptide Oatp1. (6/199)

Gadoxetate is a new hepatobiliary magnetic resonance imaging contrast agent. It is specifically taken up by hepatocytes, and its uptake can be inhibited by the coadministration of bromosulfophthalein, suggesting an involvement of one or several of the cloned organic anion transporting polypeptides Oatp1, Oatp2, and/or OATP. In this study, we demonstrated saturable uptake of gadoxetate by Oatp1 cRNA-injected Xenopus laevis oocytes (Km approximately 3.3 mM). In contrast, gadoxetate was not taken up by Oatp2 or OATP cRNA-injected oocytes. Oatp1-mediated gadoxetate uptake (100 microM) could be inhibited by 10 microM bromosulfophthalein (45%), 200 microM taurocholate (92%), 100 microM rifamycin SV (97%), and 100 microM rifampicin (51%). These results show that gadoxetate is a low-affinity substrate of Oatp1. Oatp1-mediated gadoxetate transport demonstrated a similar apparent Km value and cis-inhibition pattern as previously determined in rats in vivo, indicating that Oatp1 is significantly involved in gadoxetate uptake into rat liver.  (+info)

Kinetic modeling of slow dissociation of bromosulphophthalein from albumin in perfused rat liver: toxicological implications. (7/199)

Due to strong binding between organic anions and albumin, the kinetics of the binding process must be carefully considered in biologically-based models used for predictive toxicology applications. Specifically, the slow dissociation rate of an organic anion from the protein may lead to reduced availability of free anion in its flow through the capillaries of an organ. In this work, the effect of the dissociation rate of the anion bromosulphophthalein (BSP) from albumin was studied in isolated, perfused rat livers in the presence of albumin concentrations of 0.25, 1, and 4% (w/v) and an initial BSP concentration of 20 microM. The uptake of BSP from the perfusion medium was modeled using a biologically-based kinetic model of the sinusoidal and intracellular liver compartments. The best fit of the model to data resulted in the prediction of a slow dissociation rate constant for the BSP-albumin of between 0.097 and 0.133 s(-1). Assuming BSP and albumin to be in binding equilibrium in the sinusoidal space, with rapid binding-rate constants, as is often done, produced an unacceptable fit. These results indicate that the strong binding interaction between BSP and albumin, beyond keeping the concentration of free chemical low due to a small equilibrium dissociation constant, can also reduce uptake by an organ due to the slow release of BSP from the protein during passage through the capillaries. The implication of this dissociation-limited condition, when extrapolating to other doses and in-vivo situations, is discussed.  (+info)

Down-regulation by extracellular ATP of rat hepatocyte organic anion transport is mediated by serine phosphorylation of oatp1. (8/199)

Recent studies implicate a role in hepatocyte organic anion transport of a plasma membrane protein that has been termed oatp1 (organic anion transport protein 1). Little is known regarding mechanisms by which its transport activity is modulated in vivo. In previous studies (Campbell, C. G., Spray, D. C., and Wolkoff, A. W. (1993) J. Biol. Chem. 268, 15399-15404), we demonstrated that hepatocyte uptake of sulfobromophthalein was down-regulated by extracellular ATP. We have now found that extracellular ATP reduces the V(max) for transport of sulfobromophthalein by rat hepatocytes; K(m) remains unaltered. Reduced transport also results from incubation of hepatocytes with the phosphatase inhibitors okadaic acid and calyculin A. Immunoprecipitation of biotinylated cell surface proteins indicates that oatp1 remains on the cell surface after exposure of cells to ATP or phosphatase inhibitor, suggesting that loss of transport activity is not caused by transporter internalization. Exposure of (32)P-loaded hepatocytes to extracellular ATP results in serine phosphorylation of oatp1 with the appearance of a single major tryptic phosphopeptide; oatp1 from control cells is not phosphorylated. This phosphopeptide comigrates with one of four phosphopeptides resulting from incubation of cells with okadaic acid. These studies indicate that the phosphorylation state of oatp1 must be an important consideration when assessing alterations of its functional expression in pathobiological states.  (+info)

Sulfobromophthalein (BSP or bromsulphthalein) is not typically defined in a medical dictionary as it is a chemical compound. However, I can provide you with some information about its use in a medical context:

Sulfobromophthalein is a chemical compound primarily used for liver function tests. It is a dye that is injected into the patient's bloodstream, and then its clearance rate from the blood is measured to evaluate liver function. A healthy liver should quickly remove the dye from the blood and excrete it through the bile ducts into the digestive system. If the liver is not functioning properly, the clearance of sulfobromophthalein will be slower, leading to higher levels of the dye remaining in the bloodstream over time.

The test using sulfobromophthalein has largely been replaced by more modern and specific liver function tests; however, it was once widely used for assessing overall liver health and diagnosing conditions such as hepatitis, cirrhosis, and liver damage due to various causes.

Fluids and secretions in a medical context refer to the various liquids produced by different tissues, organs, and systems in the body. These fluids have specific compositions and functions that are essential for maintaining homeostasis and supporting physiological processes. Here are brief definitions of some key fluids and secretions:

1. Intracellular fluid (ICF): The fluid inside cells, accounting for about 65% of total body water. It contains various ions, nutrients, waste products, and organelles necessary for cell function.
2. Extracellular fluid (ECF): The fluid outside cells, making up around 35% of total body water. ECF is further divided into interstitial fluid, blood plasma, and transcellular fluid.
* Interstitial fluid: The fluid that surrounds the cells in the body, acting as a medium for exchanging nutrients, waste products, and gases between cells and blood vessels.
* Blood plasma: The liquid component of blood, containing water, ions, nutrients, waste products, hormones, gases, and proteins that help regulate fluid balance, immunity, and other vital functions.
* Transcellular fluid: Specialized fluids found in specific locations, such as cerebrospinal fluid (CSF) surrounding the brain and spinal cord, synovial fluid lubricating joints, pleural fluid surrounding lungs, pericardial fluid around the heart, and aqueous humor within the eyes.
3. Secretions: Fluids produced by glands or specialized cells, which can be classified into exocrine and endocrine secretions.
* Exocrine secretions: Fluids released through ducts to specific locations on the body's surface or into cavities. Examples include saliva from salivary glands, digestive enzymes from the pancreas, bile from the liver and gallbladder, sweat from sweat glands, and mucus from respiratory and reproductive tracts.
* Endocrine secretions: Hormones released directly into the bloodstream by endocrine glands or cells, such as insulin from the pancreas, thyroid hormones from the thyroid gland, adrenal hormones from the adrenal gland, and steroid hormones from the ovaries and testes.
4. Excretions: Waste products eliminated from the body, including urine (containing urea and other metabolic waste), feces (containing undigested food particles, bacteria, and bile pigments), sweat (containing water, salts, and small amounts of waste products), and carbon dioxide exhaled through the lungs.
5. Diapedesis: The process by which white blood cells (leukocytes) move from blood vessels into surrounding tissues to combat infection or inflammation. This occurs through gaps between endothelial cells lining blood vessel walls, allowing leukocytes to migrate towards sites of injury or infection.
6. Transudate: A clear, straw-colored fluid that forms when there is increased hydrostatic pressure or decreased oncotic (protein) pressure in the capillaries, causing leakage into surrounding tissues. This can occur due to heart failure, liver cirrhosis, or kidney disease.
7. Exudate: A cloudy, yellowish-green or brown fluid that forms when there is inflammation or infection in the body, leading to increased vascular permeability and leakage of proteins, white blood cells, and other cellular debris into surrounding tissues. This can be seen in conditions such as pneumonia, abscesses, or burns.
8. Plasma: The liquid component of blood, which carries cells (red blood cells, white blood cells, and platelets) and various substances (nutrients, hormones, waste products, gases) throughout the body. Plasma is about 90% water and 10% dissolved solutes, including proteins, electrolytes, glucose, lipids, vitamins, and gases.
9. Serum: The clear, straw-colored fluid that remains after blood clots and the clotting factors are removed. Serum contains all the dissolved substances found in plasma except for fibrinogen and other clotting factors. It is commonly used for diagnostic tests to measure various components, such as electrolytes, enzymes, hormones, antibodies, and drugs.
10. Hematocrit: The percentage of red blood cells in whole blood, measured by centrifuging a sample of blood to separate the cellular components from the plasma. A high hematocrit indicates increased numbers of red blood cells, which may be due to dehydration, living at high altitudes, or certain medical conditions like polycythemia vera. A low hematocrit suggests anemia or blood loss.
11. Hemoglobin: The iron-containing protein in red blood cells responsible for carrying oxygen from the lungs to tissues and carbon dioxide from tissues to the lungs. Each hemoglobin molecule can bind four oxygen molecules, making it highly efficient at transporting oxygen throughout the body.
12. Mean corpuscular volume (MCV): The average size of red blood cells, measured in femtoliters (fL). MCV is calculated by dividing the hematocrit by the red blood cell count. Normal values range from 80-100 fL. High MCV suggests macrocytic anemia, while low MCV indicates microcytic anemia.
13. Mean corpuscular hemoglobin (MCH): The average amount of hemoglobin in a red blood cell, measured in picograms (pg). MCH is calculated by dividing the total amount of hemoglobin by the red blood cell count. Normal values range from 27-31 pg. High MCH suggests macrocytic anemia, while low MCH indicates microcytic anemia.
14. Mean corpuscular hemoglobin concentration (MCHC): The average concentration of hemoglobin in a red blood cell, measured as a percentage. MCHC is calculated by dividing the total amount of hemoglobin by the hematocrit. Normal values range from 32-36%. High MCHC suggests hemoglobinopathies or dehydration, while low MCHC indicates iron deficiency anemia.
15. Red cell distribution width (RDW): A measure of the variation in red blood cell size, expressed as a coefficient of variation (CV). RDW is calculated by dividing the standard deviation of red blood cell volume by the MCV and multiplying by 100. Normal values range from 11-14.5%. High RDW suggests anisocytosis, which can be seen in various types of anemia, including iron deficiency anemia, megaloblastic anemia, and hemolytic anemia.
16. Platelet count: The number of platelets (thrombocytes) present in a sample of blood, expressed as cells per liter (cells/L). Normal values range from 150-450 x 10^9/L. Low platelet counts can be seen in various conditions, including vitamin B12 or folate deficiency, disseminated intravascular coagulation (DIC), and certain medications. High platelet counts can be seen in inflammatory conditions, malignancies, and certain medications.
17. Mean platelet volume (MPV): The average size of platelets in a sample of blood, expressed as femtoliters (fL). Normal values range from 7-12 fL. High MPV suggests increased platelet production or activation, which can be seen in various conditions, including inflammatory disorders, malignancies, and certain medications. Low MPV suggests decreased platelet production or increased destruction, which can be seen in various conditions, including vitamin B12 or folate deficiency, DIC, and certain medications.
18. Platelet distribution width (PDW): A measure of the variability in size of platelets in a sample of blood, expressed as a percentage. Normal values range from 10-20%. High PDW suggests increased platelet production or activation, which can be seen in various conditions, including inflammatory disorders, malignancies, and certain medications. Low PDW suggests decreased platelet production or increased destruction, which can be seen in various conditions, including vitamin B12 or folate deficiency, DIC, and certain medications.
19. Reticulocyte count: The number of reticulocytes (immature red blood cells) present in a sample of blood, expressed as a percentage of the total red blood cell count. Normal values range from 0.5-2%. High reticulocyte counts can be seen in various conditions that cause increased red blood cell production, such as hemolytic anemia or blood loss. Low reticulocyte counts can be seen in various conditions that cause decreased

Iodipamide is not typically defined in a medical dictionary or resource as it is not a medical term itself, but rather a chemical compound. Iodipamide is a radiocontrast agent that contains iodine atoms and is used during imaging procedures such as X-rays and CT scans to enhance the visibility of internal body structures.

The chemical formula for iodipamide is C8H9I5N2O2, and it is a type of organoiodine compound that is highly water-soluble and radiopaque, making it useful as a contrast agent in medical imaging. Iodipamide works by blocking X-rays and absorbing them, which allows the radiologist to see the internal structures more clearly on an X-ray or CT scan image.

While iodipamide is generally considered safe for use as a contrast agent, it can cause side effects in some people, including allergic reactions, kidney damage, and thyroid problems. As with any medical procedure, patients should discuss the risks and benefits of using iodipamide with their healthcare provider before undergoing an imaging exam.

Bilirubin is a yellowish pigment that is produced by the liver when it breaks down old red blood cells. It is a normal byproduct of hemoglobin metabolism and is usually conjugated (made water-soluble) in the liver before being excreted through the bile into the digestive system. Elevated levels of bilirubin can cause jaundice, a yellowing of the skin and eyes. Increased bilirubin levels may indicate liver disease or other medical conditions such as gallstones or hemolysis. It is also measured to assess liver function and to help diagnose various liver disorders.

Anion transport proteins are specialized membrane transport proteins that facilitate the movement of negatively charged ions, known as anions, across biological membranes. These proteins play a crucial role in maintaining ionic balance and regulating various physiological processes within the body.

There are several types of anion transport proteins, including:

1. Cl-/HCO3- exchangers (also known as anion exchangers or band 3 proteins): These transporters facilitate the exchange of chloride (Cl-) and bicarbonate (HCO3-) ions across the membrane. They are widely expressed in various tissues, including the red blood cells, gastrointestinal tract, and kidneys, where they help regulate pH, fluid balance, and electrolyte homeostasis.
2. Sulfate permeases: These transporters facilitate the movement of sulfate ions (SO42-) across membranes. They are primarily found in the epithelial cells of the kidneys, intestines, and choroid plexus, where they play a role in sulfur metabolism and absorption.
3. Cl- channels: These proteins form ion channels that allow chloride ions to pass through the membrane. They are involved in various physiological processes, such as neuronal excitability, transepithelial fluid transport, and cell volume regulation.
4. Cation-chloride cotransporters: These transporters move both cations (positively charged ions) and chloride anions together across the membrane. They are involved in regulating neuronal excitability, cell volume, and ionic balance in various tissues.

Dysfunction of anion transport proteins has been implicated in several diseases, such as cystic fibrosis (due to mutations in the CFTR Cl- channel), distal renal tubular acidosis (due to defects in Cl-/HCO3- exchangers), and some forms of epilepsy (due to abnormalities in cation-chloride cotransporters).

Indocyanine green (ICG) is a sterile, water-soluble, tricarbocyanine dye that is used as a diagnostic agent in medical imaging. It is primarily used in ophthalmology for fluorescein angiography to examine blood flow in the retina and choroid, and in cardiac surgery to assess cardiac output and perfusion. When injected into the body, ICG binds to plasma proteins and fluoresces when exposed to near-infrared light, allowing for visualization of various tissues and structures. It is excreted primarily by the liver and has a half-life of approximately 3-4 minutes in the bloodstream.

An anion is an ion that has a negative electrical charge because it has more electrons than protons. The term "anion" is derived from the Greek word "anion," which means "to go up" or "to move upward." This name reflects the fact that anions are attracted to positively charged electrodes, or anodes, and will move toward them during electrolysis.

Anions can be formed when a neutral atom or molecule gains one or more extra electrons. For example, if a chlorine atom gains an electron, it becomes a chloride anion (Cl-). Anions are important in many chemical reactions and processes, including the conduction of electricity through solutions and the formation of salts.

In medicine, anions may be relevant in certain physiological processes, such as acid-base balance. For example, the concentration of anions such as bicarbonate (HCO3-) and chloride (Cl-) in the blood can affect the pH of the body fluids and help maintain normal acid-base balance. Abnormal levels of anions may indicate the presence of certain medical conditions, such as metabolic acidosis or alkalosis.

Organic anion transporters (OATs) are membrane transport proteins that facilitate the movement of organic anions across biological membranes. The term "sodium-independent" refers to the fact that these particular OATs do not require the presence of sodium ions for their transport function.

Sodium-independent OATs are a subgroup of the larger family of organic anion transporters, which also includes sodium-dependent OATs. These transporters play important roles in the elimination and distribution of various endogenous and exogenous organic anions, including drugs, toxins, and metabolic waste products.

In the kidney, for example, sodium-independent OATs are located in the basolateral membrane of renal tubular epithelial cells and are involved in the secretion and reabsorption of organic anions. They help maintain the balance of these compounds in the body by facilitating their movement into and out of cells, often in conjunction with other transport proteins that move these compounds across the apical membrane of the tubular epithelial cells.

Overall, sodium-independent OATs are important for the proper functioning of various physiological processes, including drug disposition, toxin elimination, and waste product clearance.

Bile is a digestive fluid that is produced by the liver and stored in the gallbladder. It plays an essential role in the digestion and absorption of fats and fat-soluble vitamins in the small intestine. Bile consists of bile salts, bilirubin, cholesterol, phospholipids, electrolytes, and water.

Bile salts are amphipathic molecules that help to emulsify fats into smaller droplets, increasing their surface area and allowing for more efficient digestion by enzymes such as lipase. Bilirubin is a breakdown product of hemoglobin from red blood cells and gives bile its characteristic greenish-brown color.

Bile is released into the small intestine in response to food, particularly fats, entering the digestive tract. It helps to break down large fat molecules into smaller ones that can be absorbed through the walls of the intestines and transported to other parts of the body for energy or storage.

The liver is a large, solid organ located in the upper right portion of the abdomen, beneath the diaphragm and above the stomach. It plays a vital role in several bodily functions, including:

1. Metabolism: The liver helps to metabolize carbohydrates, fats, and proteins from the food we eat into energy and nutrients that our bodies can use.
2. Detoxification: The liver detoxifies harmful substances in the body by breaking them down into less toxic forms or excreting them through bile.
3. Synthesis: The liver synthesizes important proteins, such as albumin and clotting factors, that are necessary for proper bodily function.
4. Storage: The liver stores glucose, vitamins, and minerals that can be released when the body needs them.
5. Bile production: The liver produces bile, a digestive juice that helps to break down fats in the small intestine.
6. Immune function: The liver plays a role in the immune system by filtering out bacteria and other harmful substances from the blood.

Overall, the liver is an essential organ that plays a critical role in maintaining overall health and well-being.

Organic anion transporters (OATs) are membrane transport proteins that are responsible for the cellular uptake and excretion of various organic anions, such as drugs, toxins, and endogenous metabolites. They are found in various tissues, including the kidney, liver, and brain, where they play important roles in the elimination and detoxification of xenobiotics and endogenous compounds.

In the kidney, OATs are located in the basolateral membrane of renal tubular epithelial cells and mediate the uptake of organic anions from the blood into the cells. From there, the anions can be further transported into the urine by other transporters located in the apical membrane. In the liver, OATs are expressed in the sinusoidal membrane of hepatocytes and facilitate the uptake of organic anions from the blood into the liver cells for metabolism and excretion.

There are several isoforms of OATs that have been identified, each with distinct substrate specificities and tissue distributions. Mutations in OAT genes can lead to various diseases, including renal tubular acidosis, hypercalciuria, and drug toxicity. Therefore, understanding the function and regulation of OATs is important for developing strategies to improve drug delivery and reduce adverse drug reactions.

Biological transport refers to the movement of molecules, ions, or solutes across biological membranes or through cells in living organisms. This process is essential for maintaining homeostasis, regulating cellular functions, and enabling communication between cells. There are two main types of biological transport: passive transport and active transport.

Passive transport does not require the input of energy and includes:

1. Diffusion: The random movement of molecules from an area of high concentration to an area of low concentration until equilibrium is reached.
2. Osmosis: The diffusion of solvent molecules (usually water) across a semi-permeable membrane from an area of lower solute concentration to an area of higher solute concentration.
3. Facilitated diffusion: The assisted passage of polar or charged substances through protein channels or carriers in the cell membrane, which increases the rate of diffusion without consuming energy.

Active transport requires the input of energy (in the form of ATP) and includes:

1. Primary active transport: The direct use of ATP to move molecules against their concentration gradient, often driven by specific transport proteins called pumps.
2. Secondary active transport: The coupling of the movement of one substance down its electrochemical gradient with the uphill transport of another substance, mediated by a shared transport protein. This process is also known as co-transport or counter-transport.

Bile acids and salts are naturally occurring steroidal compounds that play a crucial role in the digestion and absorption of lipids (fats) in the body. They are produced in the liver from cholesterol and then conjugated with glycine or taurine to form bile acids, which are subsequently converted into bile salts by the addition of a sodium or potassium ion.

Bile acids and salts are stored in the gallbladder and released into the small intestine during digestion, where they help emulsify fats, allowing them to be broken down into smaller molecules that can be absorbed by the body. They also aid in the elimination of waste products from the liver and help regulate cholesterol metabolism.

Abnormalities in bile acid synthesis or transport can lead to various medical conditions, such as cholestatic liver diseases, gallstones, and diarrhea. Therefore, understanding the role of bile acids and salts in the body is essential for diagnosing and treating these disorders.

Carrier proteins, also known as transport proteins, are a type of protein that facilitates the movement of molecules across cell membranes. They are responsible for the selective and active transport of ions, sugars, amino acids, and other molecules from one side of the membrane to the other, against their concentration gradient. This process requires energy, usually in the form of ATP (adenosine triphosphate).

Carrier proteins have a specific binding site for the molecule they transport, and undergo conformational changes upon binding, which allows them to move the molecule across the membrane. Once the molecule has been transported, the carrier protein returns to its original conformation, ready to bind and transport another molecule.

Carrier proteins play a crucial role in maintaining the balance of ions and other molecules inside and outside of cells, and are essential for many physiological processes, including nerve impulse transmission, muscle contraction, and nutrient uptake.

Glutathione is a tripeptide composed of three amino acids: cysteine, glutamic acid, and glycine. It is a vital antioxidant that plays an essential role in maintaining cellular health and function. Glutathione helps protect cells from oxidative stress by neutralizing free radicals, which are unstable molecules that can damage cells and contribute to aging and diseases such as cancer, heart disease, and dementia. It also supports the immune system, detoxifies harmful substances, and regulates various cellular processes, including DNA synthesis and repair.

Glutathione is found in every cell of the body, with particularly high concentrations in the liver, lungs, and eyes. The body can produce its own glutathione, but levels may decline with age, illness, or exposure to toxins. As such, maintaining optimal glutathione levels through diet, supplementation, or other means is essential for overall health and well-being.

"Inbred strains of rats" are genetically identical rodents that have been produced through many generations of brother-sister mating. This results in a high degree of homozygosity, where the genes at any particular locus in the genome are identical in all members of the strain.

Inbred strains of rats are widely used in biomedical research because they provide a consistent and reproducible genetic background for studying various biological phenomena, including the effects of drugs, environmental factors, and genetic mutations on health and disease. Additionally, inbred strains can be used to create genetically modified models of human diseases by introducing specific mutations into their genomes.

Some commonly used inbred strains of rats include the Wistar Kyoto (WKY), Sprague-Dawley (SD), and Fischer 344 (F344) rat strains. Each strain has its own unique genetic characteristics, making them suitable for different types of research.

In the context of medicine and pharmacology, "kinetics" refers to the study of how a drug moves throughout the body, including its absorption, distribution, metabolism, and excretion (often abbreviated as ADME). This field is called "pharmacokinetics."

1. Absorption: This is the process of a drug moving from its site of administration into the bloodstream. Factors such as the route of administration (e.g., oral, intravenous, etc.), formulation, and individual physiological differences can affect absorption.

2. Distribution: Once a drug is in the bloodstream, it gets distributed throughout the body to various tissues and organs. This process is influenced by factors like blood flow, protein binding, and lipid solubility of the drug.

3. Metabolism: Drugs are often chemically modified in the body, typically in the liver, through processes known as metabolism. These changes can lead to the formation of active or inactive metabolites, which may then be further distributed, excreted, or undergo additional metabolic transformations.

4. Excretion: This is the process by which drugs and their metabolites are eliminated from the body, primarily through the kidneys (urine) and the liver (bile).

Understanding the kinetics of a drug is crucial for determining its optimal dosing regimen, potential interactions with other medications or foods, and any necessary adjustments for special populations like pediatric or geriatric patients, or those with impaired renal or hepatic function.

I. The influence of estradiol and estriol on hepatic disposal of sulfobromophthalein (BSP) in man". J Clin Invest. 43 (10): ...
I. The influence of estradiol and estriol on hepatic disposal of sulfobromophthalein (BSP) in man". J Clin Invest. 43 (10): ...
I. The Influence of Estradiol and Estriol on Hepatic Disposal of Sulfobromophthalein (BSP) in Man". The Journal of Clinical ...
... sulfobromophthalein, and other anions". Journal of Clinical Investigation. 48 (11): 2156-67. doi:10.1172/jci106182. PMC 297469 ...
... and hepatic sulfobromophthalein clearance during general anesthesia in man". J Clin Invest. J Clin Invest. 40 (3): 592-8. doi: ...
... sulfobromophthalein, and other anions". The Journal of Clinical Investigation. 48 (11): 2156-67. doi:10.1172/JCI106182. PMC ...
... the most potent are sulfobromophthalein, p-aminobenzylglutamate, and sulfathalazine. This may have pharmacological relevance in ...
... sulfobromophthalein MeSH D02.755.625.808 - thymolphthalein MeSH D02.755.684.602 - phloretin MeSH D02.755.684.602.615 - ...
Cholescintigraphy using sulfobromophthalein (BSP) have shown that the transport capacity of dye into bile is reduced by less ...
V04CD03 Sermorelin V04CD04 Corticorelin V04CD05 Somatorelin V04CD06 Macimorelin V04CE01 Galactose V04CE02 Sulfobromophthalein ...
OATP-B is the third bromosulphophthalein uptake system localized at the basolateral membrane of human hepatocytes. OATP-B, OATP-C, and OATP8 account for the major part of sodium-independent bile salt, organic anion, and drug clearance of human liver.
Increased sulfobromophthalein retention.. * Increased prothrombin and factors VII, VIII, IX and X; decreased antithrombin 3: ...
Increased sulfobromophthalein retention and other hepatic function tests.. *Coagulation tests: increase in prothrombin factors ...
I. The influence of estradiol and estriol on hepatic disposal of sulfobromophthalein (BSP) in man". J Clin Invest. 43 (10): ...
sulfobromophthalein. MTT. 3(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide. LC. liquid chromatography. HEK. human ...
DHEA-s, DHEA sulfate; BSP, sulfobromophthalein; AZT, azidothymidine (zidovudine). The values were expressed as a percentage of ... Salicylate, glutarate, penicillin G, sulfobromophthalein, taurocholate, corticosterone (a neutral steroid hormone), quinidine, ... sulfobromophthalein, penicillin G, bile salts and tetraethyl ammonium bromide. The hOAT3 protein was shown to be localized in ... sulfobromophthalein, ibuprofen, furosemide, bumetanide and azidothymidine were from Sigma (St. Louis, MO). All other chemicals ...
Probenecid decreases both hepatic and renal excretion of sulfobromophthalein (BSP). The tubular reabsorption of phosphorus is ...
Sulfobromophthalein Disodium Salt Hydrate Catalog No: 970-01 Form: Powder 970-01. Synthetic. Powder. More Info. ...
E. The following laboratory tests may be affected by progestins: hepatic function (increased sulfobromophthalein retention and ...
Pravastatin uptake into INS-1e cells was detected and this transport was inhibited by sulfobromophthalein and rifampicin, both ...
... estrone-3-sulfate and sulfobromophthalein (BSP) are transported with much lower efficiency. Gene Name:. SLCO1C1. Uniprot ID:. ...
SULFOBROMOPHTHALEIN 55600 SULFOSALICYLIC ACID 55605 SULFOXONE SODIUM 55610 SULFUR 55613 SULFURATED LIME 55615 SULINDAC 55618 ...
... methotrexate and sulfobromophthalein (BSP). Gene Name:. SLCO1B3. Uniprot ID:. Q9NPD5 Molecular weight:. 77402.2. References. * ...
A knowledge graph of biological entities such as genes, gene functions, diseases, phenotypes and chemicals. Embeddings are generated with Walking RDF and OWL method ...
Synonyms: bromosulfophthalein , BSP , sulfobromophthalein Compound class: Synthetic organic Comment: This ligand is represented ...
Read chapter 4 of Williams Manual of Hematology, 8e online now, exclusively on AccessHemOnc. AccessHemOnc is a subscription-based resource from McGraw Hill that features trusted medical content from the best minds in medicine.
Sulfobromophthalein Medicine & Life Sciences 100% * Organic Anion Transporters Medicine & Life Sciences 94% ...
Effects of perfluoroalkyl carboxylic acids on the uptake of sulfobromophthalein via organic anion transporting polypeptides in ...
Sulfobromophthalein and other liver function test values may be increased.. (g). The effects of medroxyprogesterone acetate on ...
Here it was demonstrated that oxandrolone causes the lowest sulfobromophthalein (BSP; a marker of liver stress) retention among ...
Research shows that 20mg of oxandrolone causes 72% less BSP ( Sulfobromophthalein; a marker of liver stress), compared to an ...
Mediates the Na(+)-independent transport of organic anions such as sulfobromophthalein (BSP) and conjugated (taurocholate) and ...
I. The influence of estradiol and estriol on hepatic disposal of sulfobromophthalein (BSP) in man. J Clin Invest 1964; 43(10): ...
Compared to an identical dose of fluoxymesterone, 20 mg of oxandrolone induces 72% less BSP (Sulfobromophthalein; a measure of ...
Anavar causes the lowest sulfobromophthalein retention when compared with results from Methyltestosterone, Norethandrolone, ...
Sulfobromophthalein; a marker of liver stress). ...
Cluster: AK-47 (Liver wound/sulfobromophthalein collapsing necklace), 2005-2006. Contemporary Arts Museum Houston ...

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