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ARGININE
METABOLISM
BY
ASLAM MATANIA
GROUP-3
FACULTY OF MEDICINE
TSMU
WHAT IS ARGININE?
 Arginine is an 留-amino acid
 In mammals, arginine is classified as a
semiessential or conditionally essential
amino acid, depending on the
developmental stage and health status of
the individual.
STRUCTURE
 The amino acid
side-chain of
arginine consists of
a 3-carbon aliphatic
straight chain, the
distal end of which
is capped by a
complex
guanidinium group
METABOLISM
 The two main sites of endogenous
arginine synthesis are LIVER(where
arginine is both synthesis and hydrolyzed
within urea cycle)and KIDNEY CORTEX
where most of the synthesized L-arginine
is released into blood and transported
throughout body
Cytosolic Enzyme required are-
argininosuccinate
synthetase(ASS)
andargininosuccinate
lyase(ASL)
It require 2 ATP
 synthesis of arginine occurs
in intestinalrenal axis
 which producecitrulline
fromglutamineandglutama
te,
 kidney, which extract
Arginine metabolism by  aslam matania
ARGININE PATHWAY
CITRULLINE AND ARGININE CYCLE
 The enzyme nitric oxide synthase (three
isoenzymes) cleaves the nitrogen from the
guanidino group of arginine to form NO.
 Requires NADPH, FMN, FAD, heme &
tetrahydrobiopterin(BH4)
Arginine metabolism by  aslam matania
AGMATINE
 Agmatine:
 It is a derivative of arginine produced in the
brain by decarboxylation.
 Agmatine possesses antihypertensive
properties.
Abnormalities
 Except arginase other enzyme def. in urea
cycle distrubs arginine level in the body.
 Hyperargininemia  inborn error in arginine
metabolism due to a defect in the enzyme
arginase.
 Hypoargininemia premature occurs before
the burst of cortisol production that occurs late
in preg. Cortisol is req for activation of arginine
synthetic enzymes
 Remedy + of cortisol to infant(premature)
may improve growth and survival rate
Arginine metabolism by  aslam matania

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Arginine metabolism by aslam matania

  • 2. WHAT IS ARGININE? Arginine is an 留-amino acid In mammals, arginine is classified as a semiessential or conditionally essential amino acid, depending on the developmental stage and health status of the individual.
  • 3. STRUCTURE The amino acid side-chain of arginine consists of a 3-carbon aliphatic straight chain, the distal end of which is capped by a complex guanidinium group
  • 4. METABOLISM The two main sites of endogenous arginine synthesis are LIVER(where arginine is both synthesis and hydrolyzed within urea cycle)and KIDNEY CORTEX where most of the synthesized L-arginine is released into blood and transported throughout body
  • 5. Cytosolic Enzyme required are- argininosuccinate synthetase(ASS) andargininosuccinate lyase(ASL) It require 2 ATP
  • 6. synthesis of arginine occurs in intestinalrenal axis which producecitrulline fromglutamineandglutama te, kidney, which extract
  • 10. The enzyme nitric oxide synthase (three isoenzymes) cleaves the nitrogen from the guanidino group of arginine to form NO. Requires NADPH, FMN, FAD, heme & tetrahydrobiopterin(BH4)
  • 12. AGMATINE Agmatine: It is a derivative of arginine produced in the brain by decarboxylation. Agmatine possesses antihypertensive properties.
  • 13. Abnormalities Except arginase other enzyme def. in urea cycle distrubs arginine level in the body. Hyperargininemia inborn error in arginine metabolism due to a defect in the enzyme arginase. Hypoargininemia premature occurs before the burst of cortisol production that occurs late in preg. Cortisol is req for activation of arginine synthetic enzymes Remedy + of cortisol to infant(premature) may improve growth and survival rate