The following are true about acetylcholine: a. it has a strong affinity for nicotinic receptors b. is derived from acetyl CoA and choline c. is synthesized by a reaction involving choline acetyltransferase d. all above

The following are true about acetylcholine:
a. it has a strong affinity for nicotinic receptors
b. is derived from acetyl CoA and choline
c. is synthesized by a reaction involving choline acetyltransferase
d. all above
by

1 Answer

Answer :

all above
by

Related questions

The following are true about acetylcholine: a. it is synthesized from acetyl-coenzyme A and choline b. its formation is catalysed by acetylcholinesterase c. at the synaptic cleft, it is inactivated by hydrolysis d. reuptake by the presynaptic neurones play an important in inactivating acetylcholine

Description : The following are true about acetylcholine: a. it is synthesized from acetyl-coenzyme A and choline b. its formation is catalysed by acetylcholinesterase c. at the synaptic cleft, ... inactivated by hydrolysis d. reuptake by the presynaptic neurones play an important in inactivating acetylcholine

Last Answer : at the synaptic cleft, it is inactivated by hydrolysis

Sphingosine is synthesized from (A) Palmitoyl CoA and Choline (B) Palmitoyl CoA and ethanolamine (C) Palmitoyl CoA and serine (D) Acetyl CoA and choline

Description : Sphingosine is synthesized from (A) Palmitoyl CoA and Choline (B) Palmitoyl CoA and ethanolamine (C) Palmitoyl CoA and serine (D) Acetyl CoA and choline

Last Answer : Answer : C

The following are true about acetylcholine receptors: a. receptors at all autonomic ganglia are nicotinic b. receptors at the skeletal neuromuscular junction are muscarinic c. acetylcholine receptors in the autonomic ganglia can be selectively blocked by atropine d. acetylcholine receptors in the neuromuscular junction can be selectively blocked by tubocurarine

Description : The following are true about acetylcholine receptors: a. receptors at all autonomic ganglia are nicotinic b. receptors at the skeletal neuromuscular junction are muscarinic c. ... atropine d. acetylcholine receptors in the neuromuscular junction can be selectively blocked by tubocurarine

Last Answer : acetylcholine receptors in the neuromuscular junction can be selectively blocked by tubocurarine

ADP ribosylation is the mode of action of (A) Cholera toxin (B) Acetyl choline (C) Muscerinic receptors (D) Cyclic AMP

Description : ADP ribosylation is the mode of action of (A) Cholera toxin (B) Acetyl choline (C) Muscerinic receptors (D) Cyclic AMP

Last Answer : Answer : A

Nicotinic action of acetylcholine is blocked by the drug (A) Atropine (B) Carvedilol (C) Neostigmine ( D ) d-Tubocurarine

Description : Nicotinic action of acetylcholine is blocked by the drug (A) Atropine (B) Carvedilol (C) Neostigmine ( D ) d-Tubocurarine

Last Answer : ( D ) d-Tubocurarine

In myasthenia gravis: a. the vertical muscles of the eye are more commonly involved than the horizontal muscles b. the pupil reaction to light is sluggish c. absent antibody to acetylcholine receptors exclude the diagnosis d. Cogan's twitch refers to involuntary twitching of the orbicularis

Description : In myasthenia gravis: a. the vertical muscles of the eye are more commonly involved than the horizontal muscles b. the pupil reaction to light is sluggish c. absent antibody to acetylcholine receptors exclude the diagnosis d. Cogan's twitch refers to involuntary twitching of the orbicularis

Last Answer : the vertical muscles of the eye are more commonly involved than the horizontal muscles

The following are true: a. heroin causes miosis by increasing the release of acetylcholine. b. botulinum toxin causes mydriasis by inhibiting the release of acetylcholine c. phenylephrine causes mydriasis by stimulating the alpha receptors d. amphetamine causes mydriasis by inhibiting noradrenaline reuptake

Description : The following are true: a. heroin causes miosis by increasing the release of acetylcholine. b. botulinum toxin causes mydriasis by inhibiting the release of acetylcholine c. ... mydriasis by stimulating the alpha receptors d. amphetamine causes mydriasis by inhibiting noradrenaline reuptake

Last Answer : phenylephrine causes mydriasis by stimulating the alpha receptors

Carnitine is synthesized from (A) Lysine (B) Serine (C) Choline (D) Arginine

Description : Carnitine is synthesized from (A) Lysine (B) Serine (C) Choline (D) Arginine

Last Answer : Answer : A

Glycine can be synthesized from (A) Serine (B) Choline (C) Betaine (D) All of these

Description : Glycine can be synthesized from (A) Serine (B) Choline (C) Betaine (D) All of these

Last Answer : Answer : D

Acetyl Choline causes `:-`

Description : Acetyl Choline causes `:-`

Last Answer : Acetyl Choline causes `:-` A. Bradycardia B. Tachycardia C. Both D. None

Prolactin release inhibiting hormone is believed to be (A) Serotonin (B) Norepinephrine (C) Dopanine (D) Acetyl choline

Description : Prolactin release inhibiting hormone is believed to be (A) Serotonin (B) Norepinephrine (C) Dopanine (D) Acetyl choline

Last Answer : Answer : C

Choline is not required for the formation of (A) Lecithins (B) Acetyl choline (C) Sphingomyelin (D) Cholic acid

Description : Choline is not required for the formation of (A) Lecithins (B) Acetyl choline (C) Sphingomyelin (D) Cholic acid

Last Answer : Answer : D

Following enzyme is involved in the synthesis of actylcholine (a) Choline acetyl transferase (b) Acetyl cholinesterase (c) Both (a) and (b) (d) None of the above

Description : Following enzyme is involved in the synthesis of actylcholine (a) Choline acetyl transferase (b) Acetyl cholinesterase (c) Both (a) and (b) (d) None of the above

Last Answer : Ans: A

The activity of HMG-CoA reductase is inhibited by (A) A fungal inhibitor mevastatin (B) Probucol (C) Nicotinic acid (D) Clofibrate

Description : The activity of HMG-CoA reductase is inhibited by (A) A fungal inhibitor mevastatin (B) Probucol (C) Nicotinic acid (D) Clofibrate

Last Answer : Answer : A

Select the first line hypolipidemic drug/drugs for treating hypertriglyceridemia in a subject with normal cholesterol level: A. Fibrates B. HMG-CoA reductase inhibitors C. Nicotinic acid D. Both 'A' and 'C' are correc

Description : Select the first line hypolipidemic drug/drugs for treating hypertriglyceridemia in a subject with normal cholesterol level: A. Fibrates B. HMG-CoA reductase inhibitors C. Nicotinic acid D. Both 'A' and 'C' are correc

Last Answer : D. Both 'A' and 'C' are correct

Select the most appropriate hypolipidemic drug for a patient with raised LDL-cholesterol level but normal triglyceride level: A. A HMG-CoA reductase inhibitor B. A fibric acid derivative C. Gugulipid D. Nicotinic acid

Description : Select the most appropriate hypolipidemic drug for a patient with raised LDL-cholesterol level but normal triglyceride level: A. A HMG-CoA reductase inhibitor B. A fibric acid derivative C. Gugulipid D. Nicotinic acid

Last Answer : A. A HMG-CoA reductase inhibitor

The rate limiting reaction in the lipogenic pathway is (A) Acetyl-CoA carboxylase step (B) Ketoacyl synthase step (C) Ketoacyl reductase step (D) Hydratase step

Description : The rate limiting reaction in the lipogenic pathway is (A) Acetyl-CoA carboxylase step (B) Ketoacyl synthase step (C) Ketoacyl reductase step (D) Hydratase step

Last Answer : Answer : A

Biotin is required for the reaction of CO2 with (A) Water (B) Acetyl CoA (C) NH3 (D) Incorporation of carbon 6 in purine

Description : Biotin is required for the reaction of CO2 with (A) Water (B) Acetyl CoA (C) NH3 (D) Incorporation of carbon 6 in purine

Last Answer : Answer : B

Fatty acids can not be converted into carbohydrates in the body, as the following reaction is not possible: (A) Conversion of glucose-6-phosphate into glucose (B) Fructose 1, 6 diphosphate to fructose-6- phosphate (C) Transformation of acetyl CoA to pyruvate (D) Formation of acetyl CoA from fatty acids

Description : Fatty acids can not be converted into carbohydrates in the body, as the following reaction is not possible: (A) Conversion of glucose-6-phosphate into glucose (B) Fructose 1, 6 diphosphate to ... phosphate (C) Transformation of acetyl CoA to pyruvate (D) Formation of acetyl CoA from fatty acids

Last Answer : Answer : C

Fatty acids cannot be converted into carbohydrates in the body as the following reaction is not possible. (A) Conversion of glucose-6-phosphate into glucose (B) Fructose 1,6-bisphosphate to fructose-6- phosphate (C) Transformation of acetyl CoA to pyruvate (D) Formation of acetyl CoA from fatty acids

Description : Fatty acids cannot be converted into carbohydrates in the body as the following reaction is not possible. (A) Conversion of glucose-6-phosphate into glucose (B) Fructose 1,6-bisphosphate to fructose- ... (C) Transformation of acetyl CoA to pyruvate (D) Formation of acetyl CoA from fatty acids

Last Answer : C

Long chain fatty acyl CoA esters are transported across the mitochondrial membrane by (A) cAMP (B) Prostaglandin (C) Carnitine (D) Choline

Description : Long chain fatty acyl CoA esters are transported across the mitochondrial membrane by (A) cAMP (B) Prostaglandin (C) Carnitine (D) Choline

Last Answer : Answer : C

Norepinephrine binds mainly to (A) α-Adrenergic receptors (B) β-Adrenergic receptrors (C) Muscarinic receptors (D) Nicotinic receptors

Description : Norepinephrine binds mainly to (A) α-Adrenergic receptors (B) β-Adrenergic receptrors (C) Muscarinic receptors (D) Nicotinic receptors

Last Answer : Answer : A

Following is an antagonist of ganglion type nicotinic receptors (a) Tubercurarine (b) a-bungarotoxin (c) Trimethaphan (d) All of the above

Description : Following is an antagonist of ganglion type nicotinic receptors (a) Tubercurarine (b) a-bungarotoxin (c) Trimethaphan (d) All of the above

Last Answer : Ans: C

Which of the following best describes the mechanism of action of scopolamine ? (a) Irreversible antagonist at nicotinic receptors (b) Irreversible antagonist at muscarinic receptors (c) Physiologic antagonist at muscarinic receptors (d) Reversible antagonist at muscarinic receptors (e) Reversible antagonist at nicotinic receptors

Description : Which of the following best describes the mechanism of action of scopolamine ? (a) Irreversible antagonist at nicotinic receptors (b) Irreversible antagonist at muscarinic receptors (c) ... receptors (d) Reversible antagonist at muscarinic receptors (e) Reversible antagonist at nicotinic receptors

Last Answer : Ans: D

Anthelmintic action of piperazine is due to: A. Interference with ATP generation in the worm B. Blockade of glucose uptake by the worm C. Hyperpolarization of nematode muscle by GABA agonistic action D. Depolarization of nematode muscle by activating nicotinic receptors

Description : Anthelmintic action of piperazine is due to: A. Interference with ATP generation in the worm B. Blockade of glucose uptake by the worm C. Hyperpolarization of nematode muscle by GABA agonistic action D. Depolarization of nematode muscle by activating nicotinic receptors

Last Answer : C. Hyperpolarization of nematode muscle by GABA agonistic action

Select the drug which reduces cholesterol synthesis in liver, increases expression of LDL receptors on hepatocytes and has been found to reduce mortality due to coronary artery disease: A. Simvastatin B. Nicotinic acid C. Gemfibrozil D. Colestipol (p. 577, 578) 43.1 4 3 . 1 D 43.2 4 3 . 2 C 43.3 4 3 . 3 A 43.4 4 3 . 4 A Ai

Description : Select the drug which reduces cholesterol synthesis in liver, increases expression of LDL receptors on hepatocytes and has been found to reduce mortality due to coronary artery disease: A. Simvastatin B. Nicotinic acid C. Gemfibrozil D. Colestipol (

Last Answer : A. Simvastatin

Neuromuscular blocking drugs do not produce central actions because: A. They do not cross the blood-brain barrier B. Nicotinic receptors are not present in the brain C. They are sequestrated in the periphery by tight binding to the skeletal muscles D. They do not ionise at the brain pH

Description : Neuromuscular blocking drugs do not produce central actions because: A. They do not cross the blood-brain barrier B. Nicotinic receptors are not present in the brain C. They are sequestrated in the periphery by tight binding to the skeletal muscles D. They do not ionise at the brain pH

Last Answer : A. They do not cross the blood-brain barrier

Neostigmine is preferred over physostigmine for treating myasthenia gravis because: A. It is better absorbed orally B. It has longer duration of action C. It has additional direct agonistic action on nicotinic receptors at the muscle end plate D. It penetrates blood-brain barrier

Description : Neostigmine is preferred over physostigmine for treating myasthenia gravis because: A. It is better absorbed orally B. It has longer duration of action C. It has additional direct agonistic action on nicotinic receptors at the muscle end plate D. It penetrates blood-brain barrier

Last Answer : C. It has additional direct agonistic action on nicotinic receptors at the muscle end plate

Neostigmine is preferred over physostigmine for treating myasthenia gravis because: A. It is better absorbed orally B. It has longer duration of action C. It has additional direct agonistic action on nicotinic receptors at the muscle end plate D. It penetrates blood-brain barrier

Description : Neostigmine is preferred over physostigmine for treating myasthenia gravis because: A. It is better absorbed orally B. It has longer duration of action C. It has additional direct agonistic action on nicotinic receptors at the muscle end plate D. It penetrates blood-brain barrier

Last Answer : C. It has additional direct agonistic action on nicotinic receptors at the muscle end plate

What is true in relation to drug receptors: A. All drugs act through specific receptors B. All drug receptors are located on the surface of the target cells C. Agonists induce a conformational change in the receptor D. Partial agonists have low affinity for the receptor

Description : What is true in relation to drug receptors: A. All drugs act through specific receptors B. All drug receptors are located on the surface of the target cells C. Agonists induce a conformational change in the receptor D. Partial agonists have low affinity for the receptor

Last Answer : C. Agonists induce a conformational change in the receptoR

What is true in relation to drug receptors: A. All drugs act through specific receptors B. All drug receptors are located on the surface of the target cells C. Agonists induce a conformational change in the receptor D. Partial agonists have low affinity for the receptor

Description : What is true in relation to drug receptors: A. All drugs act through specific receptors B. All drug receptors are located on the surface of the target cells C. Agonists induce a conformational change in the receptor D. Partial agonists have low affinity for the receptor

Last Answer : C. Agonists induce a conformational change in the receptor

What contain receptors for acetylcholine?

Description : What contain receptors for acetylcholine?

Last Answer : Need answer

Binding of acetylcholine to its receptors increases the permeability of cell membrane to (A) Ca++ (B) Na+ (C) K+ (D) Na+ and K+

Description : Binding of acetylcholine to its receptors increases the permeability of cell membrane to (A) Ca++ (B) Na+ (C) K+ (D) Na+ and K+

Last Answer : Answer : D

With regard to the autonomic nervous system: a. the dorsal root ganglia is made up mainly of the cell bodies of the sympathetic nerves b. the preganglionic sympathetic fibres are usually longer than preganglionic parasympathetic fibres c. acetylcholine is the neurotransmitter at the ganglia of both sympathetic and parasympathetic nervous system d. botulin toxin blocks acetylcholine receptors

Description : With regard to the autonomic nervous system: a. the dorsal root ganglia is made up mainly of the cell bodies of the sympathetic nerves b. the preganglionic sympathetic fibres ... the ganglia of both sympathetic and parasympathetic nervous system d. botulin toxin blocks acetylcholine receptors

Last Answer : the dorsal root ganglia is made up mainly of the cell bodies of the sympathetic nerves

Myasthenia Gravis is characterized by Options: 1) Decrease in acetylcholine reserve in motor nerve terminal 2) Decrease in dopamine reserve in motor nerve terminal 3) Decrease in receptors for acetylcholine 4) Decrease in dopamine receptors

Description : Myasthenia Gravis is characterized by Options: 1) Decrease in acetylcholine reserve in motor nerve terminal 2) Decrease in dopamine reserve in motor nerve terminal 3) Decrease in receptors for acetylcholine 4) Decrease in dopamine receptors

Last Answer : Correct Answer: 3) Decrease in receptors for acetylcholine

Select the prokinetic-antiemetic drug which at relatively higher doses blocks both dopamine D2 as well as 5-HT3 receptors and enhances acetylcholine release from myenteric neurones: A. Cisapride B. Prochlorperazine C. Metoclopramide D. Domperidon

Description : Select the prokinetic-antiemetic drug which at relatively higher doses blocks both dopamine D2 as well as 5-HT3 receptors and enhances acetylcholine release from myenteric neurones: A. Cisapride B. Prochlorperazine C. Metoclopramide D. Domperidon

Last Answer : C. Metoclopramide

Activation of the following type of receptors present on myenteric neurones by metoclopramide is primarily responsible for enhanced acetylcholine release improving gastric motility: A. Muscarinic M1 B. Serotonergic 5-HT3 C. Serotonergic 5-HT4 D. Dopaminergic D2

Description : Activation of the following type of receptors present on myenteric neurones by metoclopramide is primarily responsible for enhanced acetylcholine release improving gastric motility: A. Muscarinic M1 B. Serotonergic 5-HT3 C. Serotonergic 5-HT4 D. Dopaminergic D2

Last Answer : C. Serotonergic 5-HT4

Histamine H2 blockers attenuate the gastric secretory response to acetylcholine and pentagastrin as well because: A. H2 blockers block gastric mucosal cholinergic and gastrin receptors as well B. H2 blockers inhibit the proton pump in gastric mucosa C. Acetylcholine and gastrin act partly by releasing histamine in gastric mucosa D. Histamine, acetylcholine and gastrin all act through the phospholipase C-IP3:DAG pathway in gastric mucosa

Description : Histamine H2 blockers attenuate the gastric secretory response to acetylcholine and pentagastrin as well because: A. H2 blockers block gastric mucosal cholinergic and gastrin receptors as well B. H2 ... acetylcholine and gastrin all act through the phospholipase C-IP3:DAG pathway in gastric mucosa

Last Answer : C. Acetylcholine and gastrin act partly by releasing histamine in gastric mucosa

The mechanism by which neostigmine improves contraction of myasthenic muscle involves: A. Repetitive binding of the acetylcholine molecules to the same receptors at the muscle endplate B. Diffusion of acetylcholine released from motor nerve endings to a wider area activating neighbouring receptors C. Activation of motor end-plate receptors by neostigmine molecules themselves D. All of the above

Description : The mechanism by which neostigmine improves contraction of myasthenic muscle involves: A. Repetitive binding of the acetylcholine molecules to the same receptors at the muscle endplate B. Diffusion of ... Activation of motor end-plate receptors by neostigmine molecules themselves D. All of the above

Last Answer : D. All of the above

The mechanism by which neostigmine improves contraction of myasthenic muscle involves: A. Repetitive binding of the acetylcholine molecules to the same receptors at the muscle endplate B. Diffusion of acetylcholine released from motor nerve endings to a wider area activating neighbouring receptors C. Activation of motor end-plate receptors by neostigmine molecules themselves D. All of the above

Description : The mechanism by which neostigmine improves contraction of myasthenic muscle involves: A. Repetitive binding of the acetylcholine molecules to the same receptors at the muscle endplate B. Diffusion of ... Activation of motor end-plate receptors by neostigmine molecules themselves D. All of the above

Last Answer : D. All of the above

All the following statements about acetyl CoA carboxylase are true except (A) It is required for de novo synthesis of fatty acids (B) It is required for mitochondrial elongation of fatty acids (C) It is required for microsomal elongation of fatty acids (D) Insulin converts its inactive form into its active form

Description : All the following statements about acetyl CoA carboxylase are true except (A) It is required for de novo synthesis of fatty acids (B) It is required for mitochondrial elongation of fatty acids ( ... for microsomal elongation of fatty acids (D) Insulin converts its inactive form into its active form

Last Answer : Answer : B

All the following statements about acetyl CoA carboxylase are true except: (A) It is activated by citrate (B) It is inhibited by palmitoyl CoA (C) It can undergo covalent modification (D) Its dephosphorylated form is inactive

Description : All the following statements about acetyl CoA carboxylase are true except: (A) It is activated by citrate (B) It is inhibited by palmitoyl CoA (C) It can undergo covalent modification (D) Its dephosphorylated form is inactive

Last Answer : Answer : D

Which of the following statement regarding β-oxidation is true? (A) Requires β-ketoacyl CoA as a substrate (B) Forms CoA thioesters (C) Requires GTP for its activity (D) Yields acetyl CoA as a product

Description : Which of the following statement regarding β-oxidation is true? (A) Requires β-ketoacyl CoA as a substrate (B) Forms CoA thioesters (C) Requires GTP for its activity (D) Yields acetyl CoA as a product

Last Answer : Answer : A

The following are true about the thyroid hormone a. iodide ions enter the follicle cells by passive diffusion b .T4 and T3 bind to the receptors in nuclei c. thyroxine, once synthesized, is coupled to thyroglobulin until released d. a greater proportion of tri-iodothyronine is formed when iodine is deficient

Description : The following are true about the thyroid hormone a. iodide ions enter the follicle cells by passive diffusion b .T4 and T3 bind to the receptors in nuclei c. thyroxine, once ... thyroglobulin until released d. a greater proportion of tri-iodothyronine is formed when iodine is deficient

Last Answer : T4 and T3 bind to the receptors in nuclei

The most important mechanism by which gram negative bacilli acquire chloramphenicol resistance is (a) Decreased permeability into the bacterial cell (b) Acquisition of a plasmid encoded for chloramphenicol acetyl transferase (c) Lowered affinity of the bacterial ribosome for chloramphenicol (d) Switching over from ribosomal to mitochondrial protein synthesis

Description : The most important mechanism by which gram negative bacilli acquire chloramphenicol resistance is (a) Decreased permeability into the bacterial cell (b) Acquisition of a plasmid encoded ... bacterial ribosome for chloramphenicol (d) Switching over from ribosomal to mitochondrial protein synthesis

Last Answer : Ans: B

The most important mechanism by which gram negative bacilli acquire chloramphenicol resistance is: A. Decreased permeability into the bacterial cell B. Acquisition of a plasmid encoded for chloramphenicol acetyl transferase C. Lowered affinity of the bacterial ribosome for chloramphenicol D. Switching over from ribosomal to mitochondrial protein synthesi

Description : The most important mechanism by which gram negative bacilli acquire chloramphenicol resistance is: A. Decreased permeability into the bacterial cell B. Acquisition of a plasmid encoded ... the bacterial ribosome for chloramphenicol D. Switching over from ribosomal to mitochondrial protein synthesi

Last Answer : B. Acquisition of a plasmid encoded for chloramphenicol acetyl transferas

The capacity of an antihistaminic to produce sedation depends on the following except (a) Relative affinity for central versus peripheral H1 receptors (b) Ability to penetrate blood-brain barrier (c) Individual susceptibility (d) Ratio of H1 : H2 blockade produced by the drug

Description : The capacity of an antihistaminic to produce sedation depends on the following except (a) Relative affinity for central versus peripheral H1 receptors (b) Ability to penetrate blood-brain barrier (c) Individual susceptibility (d) Ratio of H1 : H2 blockade produced by the drug

Last Answer : Ans: D

What are low affinity receptors ?

Description : What are low affinity receptors ?

Last Answer : Low affinity receptors play role in regulating he intensity of IgE response.

What are high affinity receptors ?

Description : What are high affinity receptors ?

Last Answer : Mast cells and basophils express high affinity receptor. The high affinity enables it to bind with IgE, despite low serum concentration of IgE.

The capacity of an antihistaminic to produce sedation depends on the following except: A. Relative affinity for central versus peripheral H1 receptors B. Ability to penetrate blood-brain barrier C. Individual susceptibility D. Ratio of H1:H2 blockade produced by the drug

Description : The capacity of an antihistaminic to produce sedation depends on the following except: A. Relative affinity for central versus peripheral H1 receptors B. Ability to penetrate blood-brain barrier C. Individual susceptibility D. Ratio of H1:H2 blockade produced by the drug

Last Answer : D. Ratio of H1:H2 blockade produced by the drug