Can the human brain generate new neurons?
History Module: The Growth of New Neurons in the Adult Human Brain
Scientific knowledge at any given point in time can be described as the particular set of theories and models to which the scientific community currently subscribes to explain the world. What makes science so interesting is that periods of consensus, when a particular scientific paradigm predominates, are typically followed by periods of radical questioning, in which the previously received wisdom gets shaken to its foundations.
One example of such a revolution occurred in the neurosciences in the early 1990s. For over a century, scientists had agreed that in adult mammals, if nerve cells in the brain were damaged or died, unlike other cells in the body, they were not replaced. In other words, it was taken as an article of faith that new neurons never developed in the adult human brain. Each of us was born with as many neurons in our brains as we would ever have, and for the rest of our lives, the number of these neurons decreased continuously, though they could continue making new connections with one another until the day we died.
But for the past decade or so, this formerly unquestioned assumption has been gradually undermined, and recent studies indicate that certain parts of the brains of primates, including humans, may maintain their ability to produce new neurons throughout adult life.
Source: Barry L. Jacobs, Henriette van Praag, Fred H. Gage
When we speak of the ābirthā of new neurons, or neurogenesis, in the adult brain, what we are actually talking about is the process by which stem cells, such as those found in the hippocampus, divide in two. One of the two cells will remain a stem cell, while the other will turn into a neuron.
Through this process, which occurs throughout the body, cells that could potentially do anything acquire their final specialization: some become blood cells, while others become muscle or skin cells. And some others, as we now know, become functional nerve cells, with dendrites and axons that connect them to other parts of the hippocampus.
The following paragraphs review the events that led scientists to conclude that functional new neurons very likely do continue to form in the adult human brain, a process known as neurogenesis. As we shall see, a scientific revolution such as this one doesnāt usually happen overnight. More often, a body of observations accumulates gradually over a long time until it eventually refutes the original concept.
The scientific dogma that no new neurons form in the adult human brain resulted in part from experiments conducted on rhesus monkeys in the 1960s (in particular by Pasko Rakic of Yale University). These experiments focused on the development of synapses to explain the plasticity of the brain.
The first set of results that began to contradict this dogma were published in 1965. Working with adult rats, Joseph Altman and Gopal Das of the Massachusetts Institute of Technology (MIT) reported the birth of new cells in fairly primitive regions of the brain: the olfactory system and the dentate gyrus of the hippocampus. But these scientists were still uncertain whether these were neurons or glial cells.
In the 1980s, other researchers detected the appearance of new neurons in the brains of canaries that were learning new songs. Evidence began to accumulate in other experiments as well, such as an increase in the brain weight of rats after they had been trained to run labyrinths. But until the 1990s, most scientists continued to endorse the position that no new neurons ever form in the adult brain.
In the late 1980s, Elizabeth Gould, who was studying the effects of various hormones on the brain, was puzzled to observe several signs of the birth of new neurons in the rat hippocampus. She mentioned these observations in articles published in 1992 and 1993, but they drew little attention from the scientific community.
In 1996, Dr. Gould and Bruce McEwen observed that stress reduced the formation of these new neurons in the brains of rats. These observations drew more attention, because they appeared to show that the environment could influence the formation of nerve cells.
In spring 1998, Gould and her team reported having observed neurogenesis in the hippocampus and the olfactory bulbs of adult primates (marmoset monkeys). The following fall, the same observation was made in rhesus monkeys, which are even more closely related to humans. These results in rhesus monkeys were soon confirmed, in May 1999, by David R. Kornack and Pasko Rakic.
In , the team of Swedish researcher Peter Eriksson and American researcher Fred H. Gage published a study demonstrating that new neurons are generated in the dentate gyrus of the adult human brain. The study also showed that these new neurons were produced from stem cells, then migrated through the granular layer and differentiated into mature neurons with axons and dendrites.
In, Gouldās team further refined its observations by showing that the extent of neurogenesis was proportional to the amount of cognitive stimulus that the animal received from its environment. Thus, an enriched environment would promote neurogenesis while an impoverished environment would reduce it. Likewise, rats that interacted socially were found to have more new neurons than rats that were isolated in individual cages.
In, Dr. Gould published an article, in the journal Science, stating that new neurons were produced in three associative regions of the neocortex of adult rhesus monkeys: the prefrontal, inferior temporal, and posterior parietal cortexes. These regions are involved in higher cognitive functions such as decisionmaking, short-term memory, recognition of faces and the position of objects in space, and so on. Many scientists found it far harder hard to accept the idea that even this most recently evolved part of the brain could generate new neurons.
In 2000, Eriksson and Gage published another study, in which they showed that new neurons are generated in the dentate gyrus of people up to 72 years of age.
Also in 2000, other articles appeared that linked neurogenesis in the hippocampus with depression. Researchers already knew that stress slowed down neurogenesis. Now they observed that therapeutic interventions that increased the level of serotonin in the brain also increased neurogenesis. The idea that neurogenesis might play a role in precipitating and curing episodes of depression began to be discussed more and more.
In, Rakic published an article in which he contradicted Gouldās results and concluded that though neurogenesis does in fact occur in the hippocampus of adult primates, there is no compelling evidence that it does so in their neocortex. The debate on this issue continues.
In, Henriette van Praag, Fred H. Gage, and their team reported that the membranes of the new neurons generated in the hippocampus of adult mice have normal properties that enable them to propagate action potentials and form functional synapses. The finding that new neurons can develop in various parts of the brain and establish functional connections with the neurons that were already there opens new prospects for the treatment of degenerative diseases such as Alzheimerās and Parkinsonās.
Source: Heather A. Cameron
One-week-old neurons newly developed in the dentate gyrus of an adult rat brain
The story continuesā¦
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