<span>There are numerous proteins in muscle. The main two are thin actin filaments and thick myosin filaments. Thin filaments form a scaffold that thick filaments crawl up. There are many regulatory proteins such as troponin I, troponin C, and tropomyosin. There are also proteins that stabilize the cells and anchor the filaments to other cellular structures. A prime example of this is dystrophin. This protein is thought to stabilize the cell membrane during contraction and prevent it from breaking. Those who lack completely lack dystrophin have a disorder known as Duchene muscular dystrophy. This disease is characterized by muscle wasting begininng in at a young age and usually results in death by the mid 20s. The sarcomere is the repeating unit of skeletal muscle.
Muscle cells contract by interactions of myosin heads on thick filament with actin monomers on thin filament. The myosin heads bind tightly to actin monomers until ATP binds to the myosin. This causes the release of the myosin head, which subsequently swings foward and associates with an actin monomer further up the thin filament. Hydrolysis and of ATP and the release of ADP and a phosphate allows the mysosin head to pull the thick filament up the thin filament. There are roughly 500 myosin heads on each thick filament and when they repeatedly move up the thin filament, the muscle contracts. There are many regulatory proteins of this contraction. For example, troponin I, troponin C, and tropomyosin form a regulatory switch that blocks myosin heads from binding to actin monomers until a nerve impulse stimulates an influx of calcium. This causes the switch to allow the myosin to bind to the actin and allows the muscle to contract. </span><span>
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The use of electronic instruments or other techniques to monitor and change subconscious activities, many of which are regulated by the autonomic nervous system, is called biofeedback.
<h3>What is biofeedback?</h3>
A mind-body approach known as biofeedback employs a variety of monitoring tools to give the body's physical functions, which are typically controlled by the body's automatic systems, conscious control. There are several kinds of biofeedback instruments that can be used to track the development of the activity and show the efficacy of the therapy as it is being administered.
The equipment that measures the following uses biofeedback the most frequently:
- brain activity
- respiration rate
- blood pressure
- heartbeat frequency and heartbeat variability
- tension in muscles
- electrification of the skin
- skin temperature
Devices used to measure body change are:
- Electromyogram (EMG): To measure muscular tension, use this.
- Electrodermal activity (EDA): This measures variations in perspiration rate.
- Measures of finger pulses: These evaluate heart rate and blood pressure.
- Electroencephalogram (EEG): This is used to assess brain electrical activity.
Learn more about biofeedback here:
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Answer:
La pata de un pato y la aleta de un pez son en ambos casos son elementos que les permiten tanto al pato como al pez moverse, además de sus funciones de estabilidad. La aleta de una ballena y el brazo del ser humano, sucede lo mismo que en el caso anterior. En el caso de la aleta de la ballena, es como la aleta del pez. En cuanto al brazo del ser humano permite realizar movimientos que contribuyen al desarrollo de sus funciones, como por ejemplo, agarrar distintos elementos. La pelvis reducida de los cetáceos no tiene actualmente ninguna función.
Explanation:
La pata de un pato es una extremidad que por su estructura le permita nadar perfectamente. En cuanto a la aleta de los peces y ballenas, es una parte de estos animales formada por tejido conjuntivo. Pueden tener distintos tamaños y su principal función no sólo es permitir el movimiento sino también la estabilidad. En cuanto a la pelvis reducida de los cetáceos era algo que tenía sentido en especies de antaño. Durante la evolución, su utilidad de fue perdiendo, como podría mencionarse el ejemplo en los humanos de las muelas de juicio.
Big growth is
<span>macroevolution as small growth is to microevolution</span>
