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DEVELOPMENT OF THE NERVOUS SYSTEM:Post natal

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Neurological Basis of Behavior (PSY - 610)
VU
Lesson22
DEVELOPMENT OF THE NERVOUS SYSTEM
Objectives:
These lessons would familiarize the students with
·  The stages of development of the brain and the changes which takes place
·  Various stages of neuronal development.
·  Development of the brain: from the fertilization to the various developmental stages in-utero,
and postnatally.
·  Cell differtiation, determination, migration, (inside-out), cell competition, Cell death, growth
Cones, Nerve growth Factor and its role, Influences in growth and development of the brain
·  Teratogenesis Genetic anomalies which affect development of the brain.
·  Plasticity of the Nervous system.
Brain development:
Post natal
Brain development is modulated by external influences, and the interaction with external stimulation is
important for the growth of the brain. The development of behaviour matches the development of the
Central nervous System.
The brain development can be seen from the following tables
Table 1: Age and brain development and functioning
Age
Brain
Structural development and changes
Behaviours
weight
neonate  350 g
Dense cells, very few fibres
Sub cortical reflexes, moro
grasp,rooting
2-3 mos
500 g
Grey and white matter is poorly
Visuo sensory motor integrative
differentiated, not densely packed
functioning
neurons ( Nissyl staining)
6
-8 660 g
Cytoplasm more , and distinction
Higher Cognitive and cognitive
mos
between grey and white matter
functioning
8-12
925 g
Reduced cell number, increase in
Interaction
with
their
mos
neuronal/glial fibres ( for connections)
surroundings and show strange
year
anxiety
3 years
1080 g
Further reduction in cell number and
increases in cell connection
6-14
1350 g
Maturation and myelination of cells
years
continues
Motor development (movement and coordination) and sensory development are interactive. Therefore
motor stimulation inputs into the sensory and stimulates the formation of connections and action.
Similarly, the sensory input stimulates the motor connections. This leads to the development of the brain
from the neonates brain being subcortical (functioning form the reflexive systems, not the cortex) at 1
month from this the infant moves to grasp objects, raising head, smiling at familiar faces, focus on
objects, then learn to roll, sit, crawl, pick small objects with fingers, and eventually stand and walk all
within the space of a year (or a little more). It must be remembered that the development of Central
nervous Systems matches these behavioral and motor/sensory development.
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Neurological Basis of Behavior (PSY - 610)
VU
Influences which affect brain development
The brain is vulnerable to external influences during the period of rapid growth and development. We
would be talking about some of these influences. One fact must be clearly understood that the fetus does
not have any protective own mechanism of protection (except for the placental barrier). It is at the
mercy of the mother, as whatever it gets (nutrition, blood, cleaning up of toxics) is through the mother
(the umbilical cord is the connection. However, there is a critical period when the influences can affect
the brain, and the areas of the growing brain that are most vulnerable. The influences would not be
effective wither before or after the period.
Critical sensitive period
The periods within which the growth of the organism can be affected by influences i.e. the period of
development, differentiation, and proliferation. The period prior or subsequent to the critical period is
not important. The influence/substances will not affect development before/after the critical periods.
Brain most susceptible only during that period. Normal development can be affected by
presence/absence, increase /decrease in the required/normal levels. Each of the following influences has
its own critical /sensitive period, depending on where or what was required.
1. Influences:
a)
Nutrition
b)
Hormones
c)
External stimulation,
d)
Oxygen levels e) motor stimulation
e)
Viral and other diseases such as measles
Drugs, radiation, etc.
f)
Nutrition (ref Brown and Wallace, 1988).If the mother and the embryo suffer from malnutrition during
the period when brain cells are dividing rapidly, and then there is decreased division of cells leading to
decreased number of cells in the growing brain. Cells need nutrition and material to divide and grow. If
this is not available, the cells would not divide further. The sensitive period is from 2nd trimester
(gestation) to 1st year post partum (after birth). This is extended as the neurons in different areas are
developing at different times. The effect of malnutrition depends upon the time during which specific
cells are dividing (Winnick and Russo, 1975). The damage is permanent, causing irreversible damage to
the Nervous System. The multiplying neurons require proteins, NGF, other tropic factors, if this process
is blocked; this leads to the irreversible damage that researchers have reported. The damage can be
categorized as follows:
Reduced Cell size: Cells do not develop to their normal size. Histologically, we see small cells
1.
(starved cells) as compared to normal. This effect is reversible i.e. if proper nutrition is given the
cells would grow to normal size.
Reduced Cell Number: Cell division is affected by malnutrition of cells. Proliferation would not
2.
take place, as without sufficient nutrition, cells will not multiply. If nutrition is provided during the
critical period when cells are proliferating, the effects are reversible. However, once the period is
over and cellular proliferation ends, no change is possible.
Reduced Cell Connections: Connections between cells and of cells with other tissue are being
3.
formed. Therefore there is sprouting of cell extensions. If enough nutrition is not available then
there is decreased sprouting of dendrites. We must remember that in order to have an efficient
communication system, neurons need multiple connections. These input connections are provided
by the dendrites and their extensions (dendritic spines). If there is an increased number of dendritic
branching (spines), there would be large number of connections available. Thus, this results in a
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Neurological Basis of Behavior (PSY - 610)
VU
more efficient and quicker system of communication. This becomes a more intelligent and alert
young brain as it can get information from a large number of sources (it's like a computer with a
larger connectivity). Intellectual functioning is affected by reduced cell connections. However, this
is a reversible effect only if nutrition is provided within the critical period.
Myelination: Myeliantion is a fatty sheath for insulation of neuronal processes (just as electrical
4.
wires have rubber covering to insulate them). If the formation of myelin covering does not take
place it can affect the efficiency of neuronal processing and functioning. Myelin loss is not
extensively reversed by nutritional rehabilitation.
·
Severe protein deficiency: This is a selective deficiency of proteins leading to decreased
number of neurons, glial cells, dendrites, and deficient myelination of the processes. Every part
of the growing neurons is affected by protein deficiency.
·
Kwashiorkor: Is the disorder where selective protein deficiency or depletion has taken place.
The symptoms are thin muscles, but fat is present on the body, with edema on the feet etc.
·
Marasmus: Is the symptom of malnutrition (due to reduced caloric intake) in the fetus. Even if
the newborn appears physically healthy, there is irreversible brain damage. There are decreases
in brain capacity by 10-20% as a consequence of this decreased caloric intake. The Brain
weights are lesser than normal, and the brain size is smaller than normal (fewer cells)
There are also deficits due to decrease amount of. Vitamins and minerals (such as iron and potassium)
on the brain development.
Monkeberg (1975) studied 500 pre school children, relating nutrition and intellectual functioning. He
reported that in the malnourished group there were 40% children below the IQ 80. As compared to this
in the normal group were only 3% below the IQ of 80.
Interesting experiment by Weiner (1977) shows that rat mothers spend more time with their alnourished
young as compared to the healthy one.
POINTS TO PONDER:
How does the mother know the young is weak?
Hormones: Hormones affect the developing brain and body by the presence/absence or increases
/decreases in normal amounts. We are going to discuss the Sex Hormones: Androgens testosterone,
(male) Estrogens, (female), the thyroid hormones and the stress hormones and their influences on
growth, (Cotman and Mcgaugh (700-705), Brown and Wallace 428-435)
1. Androgens: The hormones are important for developing neural substrates of male organs and male
sexual behavior. The release at the appropriate time determines what reproductive organs would
grow and elaborate, but the release also primes the way the brain is organized. If prenatal androgens
are there then the organism would develop a hypothalamus which directs pituitary to release
gonadotrophin in a tonic fashion. In its absence, the pituitary has a cyclic pattern of release which is
the female pattern. If females are injected with male hormones during early preganancy, they would
have more masculinized children, i.e. females with male characteristics­ psuedohermaphrodites
(Male+female organs in females). On the other hand if male hormones are injected at prenatal
periods and later in puberty"male behaviors". Perhaps tomboys are females with androgen exposure
during early prenatal period. This could also explain Sexual preferences, sexual identity disorders
such as transvestites and transsexuals.
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Neurological Basis of Behavior (PSY - 610)
VU
2. Estrogens Do not appear to be as important for bringing about changes in the NS or body.
(This is controversial as there is evidence of feminization of male fetus and development of
female organs upon repeated injections of estrogens). The young animal would develop into a
male or female depending upon the stimulation of androgen. Those which are not exposed to
androgen will emerge with brain responses only to estrogen and not androgen and develop
typical female behavior.
3. Cretinism: This is a disorder of the growing brain caused by severe Thyroid hormone
deficiency and the child has below normal intellectual functioning. The sensitive period for
responding to thyroid is around the last trimester (6-9 months of gestation). The deficiency or
normal amounts of thyroid results in poorly developed cerebral cortex shows thyroid is
important in growth, metabolic rate, glucose absorption etc. Thus thyroxine is important in
growth. The deficiency results in decreased brain size, decreased number of neurons, axons,
dendrites, decreased connections between axons and dendrites, decreased electrical activity. If
thyroid is given within the first year of life some damages can be repaired. There is a reversible
effect if hormone therapy given early enough when presence of thyroxine important. Questions:
if Hypothyroidism is bad, is hyperthyroidism good? No, early sprouting of growth! Out of
synchronization with the body and brain development
4. Stress: Levine (1960) showed that early stress beneficial. Stress was induced through handling
or mild shock in rat young. Wit was found they matured earlier, explore more in novel
environment. These animals could cope with stress later (How is stress in rats measured?
Through their emotional responses).These rats remained undisturbed and did not defecate or
urinate with fear. The normal rats showed a typical emotional response and cannot cope with
stress and also matured later. The handling stress lead to increased secretions of
adrenocorticotropic hormones( ACTH) which leads to increased Adrenal secretion in stress
and with quicker absorption in the body ( stress immunization). This leads to an earlier
development of stress response, as the release of ACTH normally occurs at 16 days in rats, in
the stressed rats this appears at 12 days (4 days earlier).Stress can be bad too, as well as
increasing the duration of stress. Ackerman,Hofer & Weiner,1978, compared adult rats which
had been separated from mothers at 15 days) with adult rats separated from mothers at 22 days.
They report that early removal from mother leads to a high risk of ulcers, these animals also
had defective thermoregulatory systems. They could not survive in extreme cold or heat (cold
and hot challenges).
References
1. Kalat J.W (1998) Biological Psychology Brooks/ Cole Publishing
2. Carlson N.R. (2005) Foundations of Physiological Psychology Allyn and Bacon, Boston
3. Pinel, John P.J. (2003) Biopsychology (5th edition) Allyn and Bacon Singapore
4 Bloom F, Nelson and Lazerson (2001), Behavioral Neuroscience: Brain, Mind and Behaviors (3rd
edition) Worth Publishers New York
5. Bridgeman, B (1988) The Biology of Behaviour and Mind. John Wiley and Sons New York
6. Brown,T.S. And Wallace. (1980) P.M Physiological Psychology
Academic Press New York
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Table of Contents:
  1. INTRODUCTION:Descriptive, Experimental and/ or Natural Studies
  2. BRIEF HISTORICAL REVIEW:Roots of Behavioural Neurosciences
  3. SUB-SPECIALIZATIONS WITHIN THE BEHAVIORAL NEUROSCIENCES
  4. RESEARCH IN BEHAVIOURAL NEUROSCIENCES:Animal Subjects, Experimental Method
  5. EVOLUTIONARY AND GENETIC BASIS OF BEHAVIOUR:Species specific
  6. EVOLUTIONARY AND GENETIC BASIS OF BEHAVIOUR:Decent With Modification
  7. EVOLUTIONARY AND GENETIC BASIS OF BEHAVIOUR:Stereoscopic vision
  8. GENES AND EXPERIENCE:Fixed Pattern, Proteins, Genotype, Phenotypic
  9. GENES AND EXPERIENCE:Mendelian Genetics, DNA, Sex Influenced Traits
  10. GENES AND EXPERIENCE:Genetic Basis of behavior, In breeding
  11. GENES AND EXPERIENCE:Hybrid vigor, Chromosomal Abnormalities
  12. GENES AND EXPERIENCE:Behavioral Characteristics, Alcoholism
  13. RESEARCH METHODS AND TECHNIQUES OF ASSESSMENT OF BRAIN FUNCTION
  14. RESEARCH METHODS AND TECHNIQUES OF ASSESSMENT OF BRAIN FUNCTION:Activating brain
  15. RESEARCH METHODS AND TECHNIQUES OF ASSESSMENT OF BRAIN FUNCTION:Macro electrodes
  16. RESEARCH METHODS AND TECHNIQUES OF ASSESSMENT OF BRAIN FUNCTION:Water Mazes.
  17. DEVELOPMENT OF THE NERVOUS SYSTEM:Operation Head Start
  18. DEVELOPMENT OF THE NERVOUS SYSTEM:Teratology studies, Aristotle
  19. DEVELOPMENT OF THE NERVOUS SYSTEM:Stages of development, Neurulation
  20. DEVELOPMENT OF THE NERVOUS SYSTEM:Cell competition, Synaptic Rearrangement
  21. DEVELOPMENT OF THE NERVOUS SYSTEM:The issues still remain
  22. DEVELOPMENT OF THE NERVOUS SYSTEM:Post natal
  23. DEVELOPMENT OF THE NERVOUS SYSTEM:Oxygen level
  24. Basic Neuroanatomy:Brain and spinal cord, Glial cells, Oligodendrocytes
  25. Basic Neuroanatomy:Neuron Structure, Cell Soma, Cytoplasm, Nucleolus
  26. Basic Neuroanatomy:Control of molecules, Electrical charges, Proximal-distal
  27. Basic Neuroanatomy:Telencephalon, Mesencephalon. Myelencephalon
  28. Basic Neuroanatomy:Tegmentum, Substantia Nigra, MID BRAIN areas
  29. Basic Neuroanatomy:Diencephalon, Hypothalmus, Telencephalon, Frontal Lobe
  30. Basic Neurochemistry:Neurochemicals, Neuromodulator, Synaptic cleft
  31. Basic Neurochemistry:Changes in ionic gates, The direct method, Methods of Locating NT
  32. Basic Neurochemistry:Major Neurotransmitters, Mesolimbic, Metabolic degradation
  33. Basic Neurochemistry:Norepinephrine/ Noradrenaline, NA synthesis, Noadrenergic Pathways
  34. Basic Neurochemistry:NA and Feeding, NE and self stimulation: ICS
  35. Basic Neurochemistry:5HT and Behaviors, Serotonin and sleep, Other behaviours
  36. Basic Neurochemistry:ACH and Behaviors, Arousal, Drinking, Sham rage and attack
  37. Brain and Motivational States:Homeostasis, Temperature Regulation, Ectotherms
  38. Brain and Motivational States:Biological Rhythms, Circadian rhythms, Hunger/Feeding
  39. Brain and Motivational States:Gastric factors, Lipostatic theory, Neural Control of feeding
  40. Brain and Motivational States:Resting metabolic state, Individual differences
  41. Brain and Motivational States:Sleep and Dreams, Characteristics of sleep
  42. Higher Order Brain functions:Brain correlates, Language, Speech Comprehension
  43. Higher Order Brain functions:Aphasia and Dyslexia, Aphasias related to speech
  44. Higher Order Brain Functions:Principle of Mass Action, Long-term memory
  45. Higher Order Brain Functions:Brain correlates, Handedness, Frontal lobe