PHM 431 Exam 2 Questions With Correct
Answers
A |loss |of |function |mutation |in |the |gene |that |encodes |the |enzyme |glucuronyl |transferase |will |
likely |cause
A) |An |increase |in |the |risk |of |a |morphine |overdose |in |patients |having |the |mutation |if |they |were
|to |receive |morphine |for |pain |relief
B) |Accelerated |deacetylation |of |heroin |in |the |brain |leading |to |higher |morphine |concentrations |
and |an |increased |risk |for |overdose
C) |Less |efficient |alcohol |metabolism |and |higher |blood |alcohol |levels
D) |"Bioactivation" |of |heroin |to |morphine |and |increased |risk |for |morphine |overdose |- |CORRECT
|ANSWER✔✔-A) |An |increase |in |the |risk |of |a |morphine |overdose |in |patients |having |the |
mutation |if |they |were |to |receive |morphine |for |pain |relief
Genetic |variations |lead |to |increases |or |decreases |in |the |risk |for |drug |addiction. |A |loss |of |
function |mutation |(a |mutation |that |leads |to |decreased |enzyme |activitity) |in |the |gene |that |
encodes |which |of |the |following |enzymes |would |lead |to |a |decreased |risk |for |alcohol |
addicition?
A) |Alcohol |dehydrogenase
B) |CYP2E1
C) |Aldehyde |dehydrogenase
D) |Glucuronyl |transferase |- |CORRECT |ANSWER✔✔-C) |aldehyde |dehydrogenase
Smoking |marijuana |to |deliver |delta-9-THC |to |the |brain |is |more |efficient |than |orally |
administered |delta-9-THC |because:
,A) |Combustion |(smoking) |is |required |to |produce |delta-9-THC |from |cannabis |leaves
B) |No |first |pass |effect |after |smoking
C) |Delta-9-THC |is |degraded |in |the |acidic |environment |of |the |stomach
D) |Delta-9-THC |is |poorly |absorbed |from |the |small |intestine |- |CORRECT |ANSWER✔✔-B) |no |first
|pass |effect |after |smoking
Which |brain |region |is |important |for |morphine |induced |analgesia?
A) |amygdala
B) |prefrontal |cortex
C) |ventral |tegmental |area
D) |periaqueductal |gray |- |CORRECT |ANSWER✔✔-periaqueductal |gray
Increases |in |nerve |terminal |calcium |signals |which |be |associated |with |deletion |fo |which |of |the |
following |genes?
A) |Kappa |opiate |receptor |gene
B) |Alpha |subunit |of |the |GABAA |receptor
C) |Adenylate |cyclase |gene
D) |NMDA |receptor |gene |- |CORRECT |ANSWER✔✔-A) |kappa |opiate |receptor |gene
which |of |the |following |drugs |is |a |partial |agonist?
A) |morphine
B) |fentanyl
C) |methadone
, D) |meperidine |- |CORRECT |ANSWER✔✔-methadone
Alcohol |is |a |drug |with |properties |that |differentiate |it |from |other |abused |drugs. |These |unique |
properties |include:
A)Elimination |occurs |via |first |order |kinetics
B) |It |is |a |high |potency |drug
C) |Elimination |occurs |via |zero |order |kinetics
D) |Tolerance |develops |very |slowly |- |CORRECT |ANSWER✔✔-C) |elimination |occurs |via |zero |
order |kinetics
The |mechanism |by |which |endocannabinoids |suppress |neurotransmitter |release |involves:
A) |binding |to |CB1 |receptors |on |presynaptic |neurons
B) |binding |to |CB2 |receptors |on |presynaptic |neurons
C) |binding |to |CB2 |receptors |on |postsynaptic |neurons
D) |binding |to |CB2 |receptors |on |lymphocytes |- |CORRECT |ANSWER✔✔-A) |binding |to |CB1 |
receptors |on |presynaptic |neurons
Suboxone |is |a |newly |approved |drug |that |can |be |used |to |treat |morphine |or |heroin |addiction. |
Suboxone |is |useful |for |its' |intended |purpose |because |it |contains:
A) |methadone, |a |partial |opioid |receptor |agonist |that |is |orally |active |and |suppresses |
withdrawal |symptom
B) |fentanyl, |a |highly |potent |opioid |receptor |agonist |and |naltrexone, |an |opioid |receptor |
antagonist |that |is |orally |active
Answers
A |loss |of |function |mutation |in |the |gene |that |encodes |the |enzyme |glucuronyl |transferase |will |
likely |cause
A) |An |increase |in |the |risk |of |a |morphine |overdose |in |patients |having |the |mutation |if |they |were
|to |receive |morphine |for |pain |relief
B) |Accelerated |deacetylation |of |heroin |in |the |brain |leading |to |higher |morphine |concentrations |
and |an |increased |risk |for |overdose
C) |Less |efficient |alcohol |metabolism |and |higher |blood |alcohol |levels
D) |"Bioactivation" |of |heroin |to |morphine |and |increased |risk |for |morphine |overdose |- |CORRECT
|ANSWER✔✔-A) |An |increase |in |the |risk |of |a |morphine |overdose |in |patients |having |the |
mutation |if |they |were |to |receive |morphine |for |pain |relief
Genetic |variations |lead |to |increases |or |decreases |in |the |risk |for |drug |addiction. |A |loss |of |
function |mutation |(a |mutation |that |leads |to |decreased |enzyme |activitity) |in |the |gene |that |
encodes |which |of |the |following |enzymes |would |lead |to |a |decreased |risk |for |alcohol |
addicition?
A) |Alcohol |dehydrogenase
B) |CYP2E1
C) |Aldehyde |dehydrogenase
D) |Glucuronyl |transferase |- |CORRECT |ANSWER✔✔-C) |aldehyde |dehydrogenase
Smoking |marijuana |to |deliver |delta-9-THC |to |the |brain |is |more |efficient |than |orally |
administered |delta-9-THC |because:
,A) |Combustion |(smoking) |is |required |to |produce |delta-9-THC |from |cannabis |leaves
B) |No |first |pass |effect |after |smoking
C) |Delta-9-THC |is |degraded |in |the |acidic |environment |of |the |stomach
D) |Delta-9-THC |is |poorly |absorbed |from |the |small |intestine |- |CORRECT |ANSWER✔✔-B) |no |first
|pass |effect |after |smoking
Which |brain |region |is |important |for |morphine |induced |analgesia?
A) |amygdala
B) |prefrontal |cortex
C) |ventral |tegmental |area
D) |periaqueductal |gray |- |CORRECT |ANSWER✔✔-periaqueductal |gray
Increases |in |nerve |terminal |calcium |signals |which |be |associated |with |deletion |fo |which |of |the |
following |genes?
A) |Kappa |opiate |receptor |gene
B) |Alpha |subunit |of |the |GABAA |receptor
C) |Adenylate |cyclase |gene
D) |NMDA |receptor |gene |- |CORRECT |ANSWER✔✔-A) |kappa |opiate |receptor |gene
which |of |the |following |drugs |is |a |partial |agonist?
A) |morphine
B) |fentanyl
C) |methadone
, D) |meperidine |- |CORRECT |ANSWER✔✔-methadone
Alcohol |is |a |drug |with |properties |that |differentiate |it |from |other |abused |drugs. |These |unique |
properties |include:
A)Elimination |occurs |via |first |order |kinetics
B) |It |is |a |high |potency |drug
C) |Elimination |occurs |via |zero |order |kinetics
D) |Tolerance |develops |very |slowly |- |CORRECT |ANSWER✔✔-C) |elimination |occurs |via |zero |
order |kinetics
The |mechanism |by |which |endocannabinoids |suppress |neurotransmitter |release |involves:
A) |binding |to |CB1 |receptors |on |presynaptic |neurons
B) |binding |to |CB2 |receptors |on |presynaptic |neurons
C) |binding |to |CB2 |receptors |on |postsynaptic |neurons
D) |binding |to |CB2 |receptors |on |lymphocytes |- |CORRECT |ANSWER✔✔-A) |binding |to |CB1 |
receptors |on |presynaptic |neurons
Suboxone |is |a |newly |approved |drug |that |can |be |used |to |treat |morphine |or |heroin |addiction. |
Suboxone |is |useful |for |its' |intended |purpose |because |it |contains:
A) |methadone, |a |partial |opioid |receptor |agonist |that |is |orally |active |and |suppresses |
withdrawal |symptom
B) |fentanyl, |a |highly |potent |opioid |receptor |agonist |and |naltrexone, |an |opioid |receptor |
antagonist |that |is |orally |active