Environmental enrichment is the stimulation of the brain by its physical and social surroundings. Brains in richer, more stimulating environments have higher rates of synaptogenesis and more complex dendrite arbors, leading to increased brain activity. This effect takes place primarily during neurodevelopment, but also during adulthood to a lesser degree. With extra synapses there is also increased synapse activity, leading to an increased size and number of glial energy-support cells. Environmental enrichment also enhances capillary vasculation, providing the neurons and glial cells with extra energy. The neuropil
(neurons, glial cells, capillaries, combined together) expands,
thickening the cortex. Research on rodent brains suggests that
environmental enrichment may also lead to an increased rate of neurogenesis.
Research on animals finds that environmental enrichment could aid
the treatment and recovery of numerous brain-related dysfunctions,
including Alzheimer's disease and those connected to aging,
whereas a lack of stimulation might impair cognitive development.
Moreover, this research also suggests that environmental enrichment
leads to a greater level of cognitive reserve, the brain's resilience to the effects of conditions such as aging and dementia.
Research on humans suggests that lack of stimulation delays and
impairs cognitive development. Research also finds that attaining and
engaging in higher levels of education, environments in which people
participate in more challenging cognitively stimulating activities,
results in greater cognitive reserve.
Early research
Donald O. Hebb in 1947 found that rats raised as pets performed better on problem solving tests than rats raised in cages.
His research, however, did not investigate the brain nor use
standardized impoverished and enriched environments. Research doing this
first was started in 1960 at the University of California, Berkeley by Mark Rosenzweig,
who compared single rats in normal cages, and those placed in ones with
toys, ladders, tunnels, running wheels in groups. This found that
growing up in enriched environments affected enzyme cholinesterase activity. This work led in 1962 to the discovery that environmental enrichment increased cerebral cortex volume. In 1964, it was found that this was due to increased cerebral cortex thickness and greater synapse and glial numbers.
Also starting around 1960, Harry Harlow studied the effects of maternal and social deprivation on rhesus monkey infants (a form of environmental stimulus deprivation). This established the importance of social stimulation for normal cognitive and emotional development.
Synapses
Synaptogenesis
Rats raised with environmental enrichment have thicker cerebral cortices (3.3–7%) that contain 25% more synapses. This effect of environmental richness upon the brain occurs whether it is experienced immediately following birth, after weaning, or during maturity.
When synapse numbers increase in adults, they can remain high in number
even when the adults are returned to impoverished environment for 30
days
suggesting that such increases in synapse numbers are not necessarily
temporary. However, the increase in synapse numbers has been observed
generally to reduce with maturation. Stimulation affects not only synapses upon pyramidal neurons (the main projecting neurons in the cerebral cortex) but also stellate ones (that are usually interneurons). It also can affect neurons outside the brain in the retina.
Dendrite complexity
Environmental enrichment affects the complexity and length of the dendrite arbors (upon which synapses form). Higher-order dendrite branch complexity is increased in enriched environments, as can the length, in young animals, of distal branches.
Activity and energy consumption
Synapses in animals in enriched environments show evidence of increased synapse activation. Synapses tend to also be much larger. Gamma oscillations become larger in amplitude in the hippocampus.
This increased energy consumption is reflected in glial and local
capillary vasculation that provides synapses with extra energy.
- Glial cell numbers per neuron increase 12–14%
- The direct apposition area of glial cells with synapses expands by 19%
- The volume of glial cell nuclei for each synapse is higher by 37.5%
- The mean volume of mitochondria per neuron is 20% greater
- The volume of glial cell nuclei for each neuron is 63% higher
- Capillary density is increased.
- Capillaries are wider (4.35 μm compared to 4.15 μm in controls)
- Shorter distance exist between any part of the neuropil and a capillary (27.6 μm compared to 34.6 μm)
These energy related changes to the neuropil
are responsible for increasing the volume of the cerebral cortex (the
increase in synapse numbers contributes in itself hardly any extra
volume).
Motor learning stimulation
Part of the effect of environmental enrichment is providing opportunities to acquire motor skills. Research upon “acrobatic” skill learning in the rat shows that it leads to increased synapse numbers.
Maternal transmission
Environmental enrichment during pregnancy has effects upon the fetus such as accelerating its retinal development.
Neurogenesis
Environmental enrichment can also lead to the formation of neurons (at least in rats) and reverses the loss of neurons in the hippocampus and memory impairment following chronic stress. However, its relevance has been questioned for the behavioral effects of enriched environments.
Mechanisms
Enriched environments affect the expression of genes in the cerebral cortex and the hippocampus that determine neuronal structure. At the molecular level, this occurs through increased concentrations of the neurotrophins NGF, NT-3, and changes in BDNF. This alters the activation of cholinergic neurons, 5-HT, and beta-adrenolin. Another effect is to increase proteins such as synaptophysin and PSD-95 in synapses. Changes in Wnt signaling have also been found to mimic in adult mice the effects of environmental enrichment upon synapses in the hippocampus. Increase in neurons numbers could be linked to changes in VEGF.
Rehabilitation and resilience
Research
in animals suggests that environmental enrichment aids in recovery from
an array of neurological disorders and cognitive impairments. There are
two mains areas of focus: neurological rehabilitation and cognitive reserve,
the brain's resistance to the effects of exposure to physical, natural,
and social threats. Although most of these experiments used animal
subjects, mainly rodents, researchers have pointed to the affected areas
of animal brains to which human brains are most similar and used their
findings as evidence to show that humans would have comparable reactions
to enriched environments. The tests done on animals are thus meant to
represent human simulations for the following list of conditions.
Neurological rehabilitation
Autism
A
study conducted in 2011 led to the conclusion that environmental
enrichment vastly improves the cognitive ability of children with autism.
The study found that autistic children who receive olfactory and
tactile stimulation along with exercises that stimulated other paried
sensory modalities clinically improved by 42 percent while autistic
children not receiving this treatment clinically improved by just 7
percent.
The same study also showed that there was significant clinical
improvement in autistic children exposed to enriched sensorimotor
environments, and a vast majority of parents reported that their child's
quality of life was much better with the treatment.
A second study confirmed its effectiveness. The second study also
found after 6 months of sensory enrichment therapy, 21% of the children
who initially had been given an autism classification, using the Autism
Diagnostic Observation Schedule, improved to the point that, although
they remained on the autism spectrum, they no longer met the criteria
for classic autism. None of the standard care controls reached an
equivalent level of improvement. The therapy using the methodologies is titled Sensory Enrichment Therapy.
Alzheimer's disease
Through
environmental enrichment, researchers were able to enhance and
partially repair memory deficits in mice between ages of 2 to 7 months
with characteristics of Alzheimer's disease. Mice in enriched environments performed significantly better on object recognition tests and the Morris Water Maze
than they had when they were in standard environments. It was thus
concluded that environmental enrichment enhances visual and learning
memory for those with Alzheimer's.
Furthermore, it has been found that mouse models of Alzheimer's disease
that were exposed to enriched environment before amyloid onset (at 3
months of age) and then returned to their home cage for over 7 months,
showed preserved spatial memory and reduced amyloid deposition at 13
months old, when they are supposed to show dramatic memory deficits and
amyloid plaque load. These findings reveal the preventive, and
long-lasting effects of early life stimulating experience on
Alzheimer-like pathology in mice and likely reflect the capacity of
enriched environment to efficiently stimulate the cognitive reserve.
Huntington's disease
Research has indicated that environmental enrichment can help relieve motor and psychiatric deficits caused by Huntington's disease.
It also improves lost protein levels for those with the disease, and
prevents striatal and hippocampal deficits in the BDNF, located in the
hippocampus.
These findings have led researchers to suggest that environmental
enrichment has a potential to be a possible form of therapy for those
with Huntington's.
Parkinson's disease
Multiple
studies have reported that environmental enrichment for adult mice
helps relieve neuronal death, which is particularly beneficial to those
with Parkinson's disease. A more recent study shows that environmental enrichment particularly affects the nigrostriatal pathway, which is important for managing dopamine and acetylcholine levels, critical for motor deficits.
Moreover, it was found that environmental enrichment has beneficial
effects for the social implications of Parkinson's disease.
Stroke
Research done in animals has shown that subjects recovering in an enriched environment 15 days after having a stroke
had significantly improved neurobehavioral function. In addition these
same subjects showed greater capability of learning and larger infarct
post-intervention than those who were not in an enriched environment. It
was thus concluded that environmental enrichment had a considerable
beneficial effect on the learning and sensorimotor functions on animals
post-stroke.
A 2013 study also found that environmental enrichment socially benefits
patients recovering from stroke. Researchers in that study concluded
that stroke patients in enriched environments in assisted-care
facilities are much more likely to be engaging with other patients
during normal social hours instead of being alone or sleeping.
Rett syndrome
A
2008 study found that environmental enrichment was significant in
aiding recovery of motor coordination and some recovery of BDNF levels
in female mice with conditions similar to those of Rett syndrome.
Over the course of 30 weeks female mice in enriched environments showed
superior ability in motor coordination to those in standard conditions.
Although they were unable to have full motor capability, they were able
to prevent a more severe motor deficit by living in an enriched
environment. These results combined with increased levels of BDNF in the
cerebellum led researchers to conclude that an enriched environment
that stimulates areas of the motor cortex and areas of the cerebellum
having to do with motor learning is beneficial in aiding mice with Rett
syndrome.
Amblyopia
A recent study found that adult rats with amblyopia improved visual acuity two weeks after being placed into an enriched environment.
The same study showed that another two weeks after ending environmental
enrichment, the rats retained their visual acuity improvement.
Conversely, rats in a standard environment showed no improvement in
visual acuity. It was thus concluded that environmental enrichment
reduces GABA inhibition and increases BDNF expression in the visual
cortex. As a result, the growth and development of neurons and synapses
in the visual cortex were much improved due to the enriched environment.
Sensory deprivation
Studies have shown that with the help of environmental enrichment the effects of sensory deprivation
can be corrected. For example, a visual impairment known as
"dark-rearing" in the visual cortex can be prevented and rehabilitated.
In general, an enriched environment will improve, if not repair, the
sensory systems animals possess.
Lead poisoning
During development, gestation
is one of the most critical periods for exposure to any lead. Exposure
to high levels of lead at this time can lead to inferior spatial
learning performance. Studies have shown that environmental enrichment
can overturn damage to the hippocampus induced by lead exposure.
Learning and spatial memory that are dependent on the long-term
potentiation of the hippocampus are vastly improve as subjects in an
enriched environments had lower levels of lead concentration in their
hippocampi. The findings also showed that enriched environments result
in some natural protection of lead-induced brain deficits.
Chronic spinal cord injuries
Research has indicated that animals suffering from spinal cord injuries
showed significant improvement in motor capabilities even with a long
delay in treatment after the injury when exposed to environmental
enrichment.
Social interactions, exercise, and novelty all play major roles in
aiding the recovery of an injured subject. This has led to some
suggestions that the spinal cord has a continued plasticity and all
efforts must be made for enriched environments to stimulate this
plasticity in order to aid recovery.
Maternal deprivation stress
Maternal deprivation
can be caused by the abandonment by a nurturing parent at a young age.
In rodents or nonhuman primates, this leads to a higher vulnerability
for
stress-related illness.
Research suggests that environmental enrichment can reverse the effects
of maternal separation on stress reactivity, possibly by affecting the
hippocampus and the prefrontal cortex.
Child neglect
In
all children, maternal care is one of the significant influences for
hippocampal development, providing the foundation for stable and
individualized learning and memory. However, this is not the case for
those who have experienced child neglect.
Researchers determined that through environmental enrichment, a
neglected child can partially receive the same hippocampal development
and stability, albeit not at the same level as that of the presence of a
parent or guardian.
The results were comparable to those of child intervention programs,
rendering environmental enrichment a useful method for dealing with
child neglect.
Cognitive reserve
Aging
Decreased hippocampal neurogenesis is a characteristic of aging.
Environmental enrichment increases neurogenesis in aged rodents by
potentiating neuronal differentiation and new cell survival.
As a result, subjects exposed to environmental enrichment aged better
due to superior ability in retaining their levels of spatial and
learning memory.
Prenatal and perinatal cocaine exposure
Research has shown that mice exposed to environmental enrichment are less affected by the consequences of cocaine exposure
in comparison with those in standard environments. Although the levels
of dopamine in the brains of both sets of mice were relatively similar,
when both subjects were exposed to the cocaine injection, mice in
enriched environment were significantly less responsive than those in
standard environments.
It was thus concluded that both the activating and rewarding effects
are suppressed by environmental enrichment and early exposure to
environmental enrichment can help prevent drug addiction.
Humans
Though environmental enrichment research has been mostly done upon rodents, similar effects occur in primates,
and are likely to affect the human brain. However, direct research upon
human synapses and their numbers is limited since this requires histological
study of the brain. A link, however, has been found between educational
level and greater dendritic branch complexity following autopsy removal
of the brain.
Localized cerebral cortex changes
MRI detects localized cerebral cortex expansion after people learn complex tasks such as mirror reading (in this case in the right occipital cortex), three-ball juggling (bilateral mid-temporal area and left posterior intraparietal sulcus), and when medical students intensively revise for exams (bilaterally in the posterior and lateral parietal cortex).
Such changes in gray matter volume can be expected to link to changes
in synapse numbers due to the increased numbers of glial cells and the
expanded capillary vascularization needed to support their increased
energy consumption.
Institutional deprivation
Children
that receive impoverished stimulation due to being confined to cots
without social interaction or reliable caretakers in low quality orphanages show severe delays in cognitive and social development. 12% of them if adopted after 6 months of age show autistic or mildly autistic traits later at four years of age.
Some children in such impoverished orphanages at two and half years of
age still fail to produce intelligible words, though a year of foster
care enabled such children to catch up in their language in most
respects.
Catch-up in other cognitive functioning also occurs after adoption,
though problems continue in many children if this happens after the age
of 6 months.
Such children show marked differences in their brains, consistent
with research upon experiment animals, compared to children from
normally stimulating environments. They have reduced brain activity in
the orbital prefrontal cortex, amygdala, hippocampus, temporal cortex, and brain stem. They also showed less developed white matter connections between different areas in their cerebral cortices, particularly the uncinate fasciculus.
Conversely, enriching the experience of preterm infants with massage quickens the maturating of their electroencephalographic activity and their visual acuity. Moreover, as with enrichment in experimental animals, this associates with an increase in IGF-1.
Cognitive reserve and resilience
Another source of evidence for the effect of environment stimulation upon the human brain is cognitive reserve
(a measure of the brain’s resilience to cognitive impairment) and the
level of a person’s education. Not only is higher education linked to a
more cognitively demanding educational experience, but it also
correlates with a person’s general engagement in cognitively demanding
activities. The more education a person has received, the less the effects of aging, dementia, white matter hyperintensities, MRI-defined brain infarcts, Alzheimer's disease, and traumatic brain injury. Also, aging and dementia are less in those that engage in complex cognitive tasks. The cognitive decline of those with epilepsy could also be affected by the level of a person’s education.