The Brain (Kapitel 4) Flashcards

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1
Q

Name the 6 criteria for a substance to be considered a classic neurotransmitter.

A
  • The substance exists in presynaptic axon terminals
  • The presynaptic cell contain appropriate enzymes for synthesizing the substance.
  • The substance is released in significant quantities when action potentials reach the terminals.
  • Specific receptors that recognize the released substance exists on the postsynaptic membrane.
  • Experimental application of the substance produces changes in postsynaptic cells.
  • Blocking release of the substance prevents presynaptic activity from affecting the postsynaptic cell. (p. 92)
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2
Q

Name the types (categories) of neurotransmitters that are often seen in the brain.

A

Amine Neurotransmitters
Amino acid neurotransmitters
Peptide neurotransmitters (or neuropeptides)
Gas neurotransmitters. (p. 92)

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3
Q

Name some Amine Neurotransmitters

A

Acetylcholine, dopamin & serotonin

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4
Q

Name some Amino acid neurotransmitters

A

GABA, glutamate

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5
Q

What is peptide neurotransmitters made of? And name some.

A

made up of short chains of amino acids.
Ex. Opioid peptides : Enkeplalin, Endorphins, Dynorphins.
Other: Oxytocin, Substance P, cholecystokinin ect.

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6
Q

What is the difference between ionotropic (also called ligand-gated ion channel) receptors and metabotropic receptors?

A

In ionotropic receptors neurotransmitters open the ion channel directly in the postsynaptic cell’s membrane. - They are fast receptors

At metabotropic receptors the neurotransmitters, activate the receptor which further activates G-proteins that open other ion channels and/or cause other changes in the postsynaptic cell. - The are slow receptors (p. 93)

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7
Q

What is a ligand?

A

A substance that binds to receptor molecules, such as those at the surface of the cell.

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8
Q

A ligand can have three types of effects. Name the three and explain them.

A

1) - AGONIST - A ligand that is classified as an agonist initiates the normal effects of the transmitter on that receptor.
2) ANTAGONIST- A recepter antagonist is a lignad that binds to a receptor and does not activate it, thereby blocking it from being activated by other ligands.
3) INVERSE AGONISTS - An inverse agonist (a less common type of ligand) binds to the receptor and initiates an effect that is the reverse of the normal function of the receptor. (p. 94)

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9
Q

Explain the difference between competitive and noncompetitive ligands.

A

Competitive ligands bind the the same part of the receptor complex that the endogenous transmitter normally would. (Doesn’t let other transmitter to the receptor)

Noncompetitive ligands binds to a modulatory site on the receptor so other transmitters can access the receptor. (p. 94)

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10
Q

There are two families of ACh-receptors in the peripheral and central nervous systems. What are they called?

A

Nicotinic and muscarinic receptors.

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11
Q

Can anyone beat Sebastian 1on1 mid?

A

No. (Første mosebog 1:1; De ti bud 1/10)

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12
Q

Name some general characteristics of nicotinic and muscarinic receptors.

A

Most nicotinic receptors are ionotropic, responding rapidly and usually having an excitatory effect.

Muscarinic ACh receptors are G protein-coupled (metabotropic) receptors, so they have slower responses when activated, and they can be either excitatory or inhibitory. (p. 95)

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13
Q

Name the two principal classes of monoamines

A

Catecholmanines and indoleamines.

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14
Q

Explain why Catecholmanines and indoleamines are called monoamines.

A

Because both neurotransmitters are modified amino acids.

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15
Q

Name the 3 catecholamine neurotransmitters

A

Dopamine, Epinephrine and Norepinephrine (They are all derived from the amino acid tyrosine)

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16
Q

Name the 2 indoleamine neurotransmitters

A

Melatonin and serotonin (they are both derived from the amoni acid tryptophan) (p. 95).

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17
Q

What are the two dopaminergic pathways in the brain?

A

Mesostriatal pathway: Substantia nigra to striatum (caudate and putamen)
Mesolimbocortical pathway: Ventral tegmental area (VTA) to nucleus accumbens, cortex (including the insula) and hippocampus. Look at the picture @ p. 95.

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18
Q

Name the two main clusters of neurons in the brainstem releasing norepinephrine.

A

Locus coeruleus, in the pons.

and the lateral tegmental system of the midbrain.

19
Q

What is the difference between norepinephrine and noradrenaline?

A

There are none. Norepinephrine is also known as noradrenaline, which is why NE-producing cells are said to be noradrenergic.

20
Q

What neurotransmitter is abbreviated 5-HT?

A

Serotonin, because the chemical name is 5-hydroxytrptamine.

21
Q

Where are the 5-HT cell bodies concentrated?

A

Along the midline in the raphe (“rafay”) nuclei of the midbrain and brainstem.

22
Q

Is it true that generally many neurons in the brain are serotonergic?

A

No. Only 200,000 of the 100 billion neurons are serotonergic.
However they do exert widespread influence through the rest of the brain.

23
Q

Name some of the human functions that serotonin has been implicated in.

A

The control of sleep states, mood, sexual behavior, anxiety, and many other functions. (p. 97).

24
Q

What is the most common transmitters in the brain?

A

Amino acids.

25
Q

Name some amino acids. And name wether they are inhibitory or excitatory

A

Glutamate and aspartate are important excitattory neurotransmitter.
GABA (Gamma-aminobutyric acid) and glycine typically have an inhibitory effect. (p. 97)

26
Q

Name which receptors glutamatergic transmission employs.

A

AMPA, kainate, and NMDA receptors.

These receptors are implicated in different functions - read of these @ p. 97.

27
Q

GABA receptors are also divided into large classes, which all exhibit quite different properties. Name the classes and their properties.

A

GABA_a: ionotropic, produces fast inhibitory postsynaptic potentials.
GABA_b: Metabotropic receptors, typically producing slow-occuring inhibitory postsynaptic potential.
GABA_c: ionotropic with a chloride channel, they differ from other GABA receptors in certain details of their subunit structure. (p. 97f).

28
Q

Many peptides function as neurotransmitters. Three types are relevant in the book. Name them.

A
  • The opioid peptides.
  • A group found in the gut and spinal cord or brain, including substance P, cholecystokinin, neurotensin etc.
  • Pituitary hormones such as oxytocin and vasopressin etc. (p. 98)
29
Q

Name the primary ways drugs can affect the brain.

A

By altering enzyme action or modifying other internal cellular processes. But most drugs of interest in biological psychology are receptor ligands. (p. 98)

30
Q

What is a good analogy to describe how drugs interact with receptors?

A

Drugs fit like keys into molecular locks.

Drug molecules do not seek out particular receptor molecules; rather, drug molecules spread widely throughout the body, and when they come in contact with a receptor molecule possessing the correct shape, the two molecules bind together briefly and begin a chain of events. (p. 99).

31
Q

What is meant by the binding affinity of a drug?

A

A drug with high affinity for a particular type of receptor will selectively bind to that type of receptor even at low doses, at it will stay bound for a relatively long time.

Low affinity drugs will bind fewer receptor molecules. (p. 100)

32
Q

What is meant by the term: efficacy, when talking about ligands?

A

The propensity of a ligand to activate the receptor to which it is bound is termed efficacy.
Agonists have high efficacy and antagonists have low efficacy. (p. 100)

33
Q

Why is affinity and efficacy important?

A

It is a combination of affinity and efficacy that determines the overall action of a drug, which is especially important to determine the right dose of the drug. (p. 100f)

34
Q

Does a specific drug always have the same potency?

A

No. The body often adapts to the administered drug: Makes drug tolerance. (p. 101)

35
Q

Name different types of tolerances.

A

Metabolic tolerance: The body’s metabolic systems and organs (such as the liver) become increasingly effective at eliminating the drug.

Functional tolerance: The target tissue show altered sensitivity to the drug. Ex. the receptor proteins to a specific drug may down-regulate or up-regulate. Depending on wether the drug is an agonist or antagonist. (p. 101f)

36
Q

Does the body always build tolerance towards drugs?

A

No. Some drug responses can become stronger with repeated treatments. Termed sensitization. (p. 102)

37
Q

Name the four routes of administering drugs.

A

Ingestion, Inhalation, Peripheral injection and Central injection. (p. 103)

38
Q

Drugs can target both/either the presynaptic cell and/or the postsynaptic cell. Name ways the presynaptic cell can be affected.

A

The drug can affect the transmitter production, transmitter release and transmitter clearance (the reuptake or degradation of transmitters) (p. 105)

39
Q

Drugs can target both/either the presynaptic cell and/or the postsynaptic cell. Name ways the postsynaptic cell can be affected.

A

Effects on the transmitter receptors and effects on the cellular processes. (p. 107)

40
Q

Drugs that affect the brain can be divided into functional classes. Name the classes

A

Antipsychotic drugs - Relieve the symptoms of schizophrenia.
Antidepressants - Relieve chronic mood problems.
Anxiolytics - Combat anxiety
Alcohol - Has several effects.
Opiates - Help relieve pain.
Cannabiniods - have a wide array of effects.
Stimulants - Increase the activity of the nervous system
Hallucinogenic and dissociative drugs - alter sensory perception. p. 107-116.

41
Q

Should you read about the different variaties of functional drugs?

A

Maybe.. If you want to read p. 107-116.

42
Q

Comprehensive models of drug abuse has been made, that each tries to answer the questions: What social and environmental factors cause someone to start abusing a substance? What factors cause the person to continue? What physiological mechanisms make a substance rewarding? What is addiction, physiologically and behaviorally? Name the 4 different models

A

The moral model: Simply blaming the substance abuser for a failure of moral character / lack of self-control.

The disease model: The person who abuses drugs requires medical treatment rather than moral exhortation or punishment.

The physical dependence model: Argues that people keep taking drugs in order to avoid unpleasant withdrawal symptoms.

The postive reward model: Proposes that people get started with drug abuse, and become addicted, because the abused drug provides powerful reinforcement. (p. 116-118)

43
Q

Name brainareas that are affiliated with addiction.

A

Many addictive drugs cause release of dopamine in nucleus accumbens.
The dopaminergic pathway from the VTA to the nucleus accumbens serves as a reward system. So its most like the neural pathway VTA –> Amygdala –> Nucleus accumbens. (p. 118f)
Insula may also be involved in addiction, as people with damage to insula have no problem quitting smoking.