Answer:
Suppose that at a given point along a capillary, the following forces exist: Capillary hydrostatic pressure (HPc) = 30 mmHg Interstitial fluid hydrostatic pressure (HPif) = 0 mmHg Capillary colloid osmotic pressure (OPc) = 25 mmHg Interstitial fluid colloid osmotic pressure (OPif) = 2 mmHg. The net filtration pressure at this point in the capillary is <u>7mmHg.</u>
Explanation:
Capillary hydrostatic pressure (HPc) = 30 mmHg
Interstitial fluid hydrostatic pressure (HPif) = 0 mmHg
Capillary colloid osmotic pressure (OPc) = 25 mmHg
Interstitial fluid colloid osmotic pressure (OPif) = 2 mmHg
Net filtration pressure= hydrostatic pressure gradient - Oncotic pressure gradient
Hydrostatic pressure gradient = Capillary hydrostatic pressure - Interstitial hydrostatic pressure = 30mmHg - 0 mmHg = 30 mmHg
Oncotic pressure gradient = Capillary colloid osmotic pressure - Interstitial fluid colloid osmotic pressure =25 - 2 = 23 mmHg
Net filtration pressure= hydrostatic pressure gradient - Oncotic pressure gradient = 30 mmHg - 23 mmHg = 7 mmHg.
Hence, The net filtration pressure at this point in the capillary is <u>7mmHg.</u>
Answer:
The options
A. Additional cables
B. Slip rings
C. Multiple rows of detectors
D. Electron beam CT.
The CORRECT ANSWER IS B.
B. Slip rings
Explanation:
During the 1990s, the use of slip ring technology promoted consecutive rotation of the x-ray tube (via removal of cables) and concurrent couch locomotion.
The Sixth-generation CT scanning is referred to as helical (or spiral) CT—allowing procurement of volume multislice scanning.
Today's helical multislice scanners, makes use of thousands of detectors (around 60+ rows), can derive continuous data procurement of 128 "slices" per tube rotation and can undergo 3D multiplanar reformation (MPR).
Fifth-generation CT employs electron beam; as the ultra high-speed CT is employed majorly for cardiac imaging.
Answer:
Pseudopodia are temporary and cytoplasm-filled parts of the cell membrane that are able to change their form in order to move.
Explanation:
Pseudopodia are temporary and cytoplasm-filled parts of the cell membrane that are able to change their form in order to move. They are used in some eukaryotic cells to move around or to eat. Most cells that do this are called amoeboids. The amoeba is a common example. ... Pseudopods can also capture prey by phagocytosis.
Explanation:
-Q. <em>How do membrane proteins aid in the movement of hydrophilic substances across the membrane?</em>
Transport proteins spanning the plasma membrane facilitate the movement of ions and other complex, polar molecules which are typically prevented from moving across the membrane from the extracellular or intracellular space.
Lipids are composed of fatty acids which form the hydrophobic tail and glycerol which forms the hydrophilic head; glycerol is a 3-Carbon alcohol which is water soluble, while the fatty acid tail is a long chain hydrocarbon (hydrogens attached to a carbon backbone) with up to 36 carbons.
Their polarity or arrangement can give these non-polar macromolecules hydrophilic and hydrophobic properties. Via diffusion, small water molecules can move across the phospholipid bilayer acts as a semi-permeable membrane into the extracellular fluid or the cytoplasm which are both hydrophilic and contain large concentrations of polar water molecules or other water-soluble compounds. The hydrophilic heads of the bilayer are attracted to water while their water-repellent hydrophobic tails face towards each other- allowing molecules of water to diffuse across the membrane along the concentration gradient.
Similarly via osmosis, molecules of water pass through the membrane due to the difference in osmotic pressure on either side of the phospholipid by layer this means that the water moves from regions of high osmotic pressure/concentration to regions of low pressure/ concentration to a steady state.
Transmembrane proteins are embedded within the membrane from the extracellular fluid to the cytoplasm, and are sometimes attached to glycoproteins (proteins attached to carbohydrates) which function as cell surface markers. Transport proteins are transmembrane proteins involed in moving molecules across the membrane.
There are two types:
- Channels or pores are filled with water, enabling charged molecules to diffuse across the membrane, from regions of high concentration to regions of lower concentration down the concentration gradient -this is a passive part of facilitated diffusion. Channels may undergo minor changes to become open or closed whereas pores are always in open states <em>e.g. H2O movement into and out of the cell via aquaporins.</em>
- Carrier proteins bind specifically bind to molecules and move them across or against concentration gradients. Unlike facilitated diffusion, carrier proteins directly or indirectly use energy in the form of ATP and modify solute specific regions, that aid in regulating ion exchange, through the hydrophobic layer of the plasma membrane- this is called <em>active transport.</em> <em>e.g. Na+/K+transported by the enzyme ATPase </em>
<em>Learn more about membrane components at brainly.com/question/1971706</em>
<em>Learn more about plasma membrane transport at brainly.com/question/11410881</em>
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