Athletes who consume adequate carbohydrates experience adequate liver and muscle glycogen stores.
<h3>What is glycogen?</h3>
Glycogen is a polysaccharide (carbohydrate) composed of many monosaccharide subunits.
Glycogen is a carbohydrate that serves as energy storage in animal cells and human cells.
During muscle contraction, glycogen is used to carry out cellular respiration and thus produce ATP.
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- The phrenic nerve is derived from the cervical plexus and receives innervation from the C3, C4, and C5 nerve roots. It is the longest branch of the cervical plexus.
Why does phrenic nerve supply diaphragm?
- The C3-C5 spinal nerves in the neck give rise to the phrenic nerve, a mixed motor and sensory nerve.
- The diaphragm, the main muscle of respiration, is exclusively controlled by the nerve, making it essential for breathing.
What organ does this nerve supply?.
- The jejunum receives both intrinsic and extrinsic nerve supply.
- The preganglionic parasympathetic and postganglionic sympathetic branches of the celiac plexus provide the autonomic extrinsic supply.
- These neurons go via branches of the major vessels from the mesentery into the jejunum.
What are the 4 types of nerves?
It is conventional, however, to describe nerve types on the basis of their function: motor, sensory, autonomic or cranial.
- Motor Nerves.
- Sensory Nerves.
- Autonomic Nerves.
- Cranial Nerves.
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Answer:
The answer is Honey.
Explanation:
For my concept the best sweetener is and will continue to be honey, because it is a natural product without any other chemical or preparation components that alter its natural condition.
Answer:
Okay
Explanation:
Human topoisomerase I plays an important role in removing positive DNA supercoils that accumulate ahead of replication forks. It also is the target for camptothecin-based anticancer drugs that act by increasing levels of topoisomerase I-mediated DNA scission. Evidence suggests that cleavage events most likely to generate permanent genomic damage are those that occur ahead of DNA tracking systems. Therefore, it is important to characterize the ability of topoisomerase I to cleave positively supercoiled DNA. Results confirm that the human enzyme maintains higher levels of cleavage with positively as opposed to negatively supercoiled substrates in the absence or presence of anticancer drugs. Enhanced drug efficacy on positively supercoiled DNA is due primarily to an increase in baseline levels of cleavage. Sites of topoisomerase I-mediated DNA cleavage do not appear to be affected by supercoil geometry. However, rates of ligation are slower with positively supercoiled substrates. Finally, intercalators enhance topoisomerase I-mediated cleavage of negatively supercoiled substrates but not positively supercoiled or linear DNA. We suggest that these compounds act by altering the perceived topological state of the double helix, making underwound DNA appear to be overwound to the enzyme, and propose that these compounds be referred to as ‘topological poisons of topoisomerase I’
