Answer:
Until recently, most neuroscientists thought we were born with all the neurons we were ever going to have. As children we might produce some new neurons to help build the pathways - called neural circuits - that act as information highways between different areas of the brain. But scientists believed that once a neural circuit was in place, adding any new neurons would disrupt the flow of information and disable the brain’s communication system.
In 1962, scientist Joseph Altman challenged this belief when he saw evidence of neurogenesis (the birth of neurons) in a region of the adult rat brain called the hippocampus. He later reported that newborn neurons migrated from their birthplace in the hippocampus to other parts of the brain. In 1979, another scientist, Michael Kaplan, confirmed Altman’s findings in the rat brain, and in 1983 he found neural precursor cells in the forebrain of an adult monkey.
These discoveries about neurogenesis in the adult brain were surprising to other researchers who didn’t think they could be true in humans. But in the early 1980s, a scientist trying to understand how birds learn to sing suggested that neuroscientists look again at neurogenesis in the adult brain and begin to see how it might make sense. In a series of experiments, Fernando Nottebohm and his research team showed that the numbers of neurons in the forebrains of male canaries dramatically increased during the mating season. This was the same time in which the birds had to learn new songs to attract females.
Why did these bird brains add neurons at such a critical time in learning? Nottebohm believed it was because fresh neurons helped store new song patterns within the neural circuits of the forebrain, the area of the brain that controls complex behaviors. These new neurons made learning possible. If birds made new neurons to help them remember and learn, Nottebohm thought the brains of mammals might too.
Other scientists believed these findings could not apply to mammals, but Elizabeth Gould later found evidence of newborn neurons in a distinct area of the brain in monkeys, and Fred Gage and Peter Eriksson showed that the adult human brain produced new neurons in a similar area.
For some neuroscientists, neurogenesis in the adult brain is still an unproven theory. But others think the evidence offers intriguing possibilities about the role of adult-generated neurons in learning and memory.
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People will have a harder time exchanging goods and services and many businesses will shut down as a result.
Answer:
d. all of the above
Explanation:
The diencephalon is a part of the brain located inferiorly and anteriorly to the corpus callosum, part of the telencephalon, and superior to the midbrain, delimited by the latter by an imaginary line that runs from the nipple to the posterior commissure (epithalamus). The diencephalon consists of: thalamus, hypothalamus, epithalamus, metatalamus and subthalamus. For this reason, we can conclude that the correct answer to your question is "d. All of the above".
Answer:
As the outer layer of your skin separates your body from its environment, the cell membrane (also known as the plasma membrane) separates the inner contents of a cell from its exterior environment. This cell membrane provides a protective barrier around the cell and regulates which materials can pass in or out.
Explanation:
Answer:
The correct option is A. Steroid hormones exert their action by entering the nucleus of a cell and initiating or altering the expression of a gene.
Explanation:
Steroid hormones are derived from cholesterol and regulate multiple biological processes. All steroid hormones exert their action by crossing the plasma membrane and by binding with their respective intracellular receptors. They stimulate cell growth in a very different way, their lipophilic nature gives them the ability to cross lipid barriers, so, without the need for extracellular signals, these hormones can easily enter the cell, cross the cytoplasm and reach the nucleus. There they bind to specific receptors that are associated with DNA promoter regions, modifying their structure and promoting the expression of the genes under their control.
