i use an extra 20-30mgs ed
Glutamine
From Wikipedia, the free encyclopedia
"Gln" redirects here. For other uses, see GLN (disambiguation).
L-Glutamine
Skeletal formula of the L-isomer
Ball-and-stick model of the L-isomer as a zwitterion
IUPAC name[hide]
Glutamine
Other names[hide]
L-Glutamine
(levo)glutamide
2-Amino-4-carbamoylbutanoic acid
Identifiers
Abbreviations Gln, Q
CAS number 56-85-9 Yes
PubChem 738
ChemSpider 718 Yes
UNII 0RH81L854J Yes
EC-number 200-292-1
KEGG C00303 Yes
ChEBI CHEBI:28300 Yes
ChEMBL CHEMBL930
IUPHAR ligand 723
ATC code A16AA03
Jmol-3D images Image 1
SMILES
[show]
InChI
[show]
Properties[1]
Molecular formula C5H10N2O3
Molar mass 146.14 g mol−1
Melting point decomposes around 185°C
Solubility in water soluble
Chiral rotation [α]D +6.5ş (H2O, c = 2)
Supplementary data page
Structure and
properties n, εr, etc.
Thermodynamic
data Phase behaviour
Solid, liquid, gas
Spectral data UV, IR, NMR, MS
Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
(verify) (what is: Yes/?)
Infobox references
Glutamine (abbreviated as Gln or Q) is one of the 20 amino acids encoded by the standard genetic code. It is not recognized as an essential amino acid. Its side-chain is an amide formed by replacing the side-chain hydroxyl of glutamic acid with an amine functional group, making it the amide of glutamic acid. Its codons are CAA and CAG. In human blood, glutamine is the most abundant free amino acid, with a concentration of about 500–900 µmol/l.[2]
Contents [hide]
1 Structure
2 Functions
2.1 Producing and consuming organs
2.1.1 Producers
2.1.2 Consumers
2.2 Examples for the usage of glutamine
2.2.1 Aiding recovery after surgery
3 Nutrition
3.1 Occurrences in nature
3.1.1 Dietary sources
4 See also
5 References
6 External links
Structure[edit]
Glutamine zwitterionic forms at neutral pH: L-glutamine (left) and D-glutamine
Functions[edit]
Glutamine plays a role in a variety of biochemical functions:
Protein synthesis, as any other of the 20 proteinogenic amino acids
Regulation of acid-base balance in the kidney by producing ammonium[3]
Cellular energy, as a source, next to glucose[4]
Nitrogen donation for many anabolic processes, including the synthesis of purines[2]
Carbon donation, as a source, refilling the citric acid cycle[5]
Nontoxic transporter of ammonia in the blood circulation
Producing and consuming organs[edit]
Producers[edit]
Glutamine is synthesized by the enzyme glutamine synthetase from glutamate and ammonia. The most relevant glutamine-producing tissue is the muscle mass, accounting for about 90% of all glutamine synthesized. Glutamine is also released, in small amounts, by the lung and the brain.[6] Although the liver is capable of relevant glutamine synthesis, its role in glutamine metabolism is more regulatory than producing, since the liver takes up large amounts of glutamine derived from the gut.[2]
Consumers[edit]
The most eager consumers of glutamine are the cells of intestines,[2] the kidney cells for the acid-base balance, activated immune cells,[7] and many cancer cells.[5] In respect to the last point mentioned, different glutamine analogues, such as DON, Azaserine or Acivicin, are tested as anticancer drugs.
Examples for the usage of glutamine[edit]
In catabolic states of injury and illness, glutamine becomes conditionally essential (requiring intake from food or supplements).[8] Glutamine has been studied extensively over the past 10–15 years, and has been shown to be useful in treatment of injuries, trauma, burns, and treatment-related side effects of cancer, as well as in wound healing for postoperative patients. Glutamine is also marketed as a supplement used for muscle growth in weightlifting, bodybuilding, endurance, and other sports. Evidence indicates glutamine, when orally loaded, may increase plasma HGH levels by stimulating the anterior pituitary gland.[9] In biological research, L-glutamine is commonly added to the media in cell culture.[10][11] However, the high level of glutamine in the culture media may inhibit other amino acid transport activities.[12]
Aiding recovery after surgery[edit]
Glutamine is also known to have various side effects in reducing healing time after operations. Hospital-stay times after abdominal surgery can be reduced by providing parenteral nutrition regimens containing high amounts of glutamine to patients. Clinical trials have revealed patients on supplementation regimens containing glutamine have improved nitrogen balances, generation of cysteinyl-leukotrienes from polymorphonuclear neutrophil granulocytes, and improved lymphocyte recovery and intestinal permeability (in postoperative patients), in comparison to those that have no glutamine within their dietary regimen, all without any side effects.[13]
Nutrition[edit]
Occurrences in nature[edit]
Glutamine is the most abundant naturally occurring, nonessential amino acid in the human body, and one of the few amino acids that can directly cross the blood–brain barrier.[14] In the body, it is found circulating in the blood, as well as stored in the skeletal muscles. It becomes conditionally essential (requiring intake from food or supplements) in states of illness or injury.[8]
Dietary sources[edit]
Dietary sources of L-glutamine include beef, chicken, fish, eggs, milk, dairy products, wheat, cabbage, beets, beans, spinach, and parsley. Small amounts of free L-glutamine are also found in vegetable juices.[8]
See also[edit]
Isoglutamine
Glutamine
From Wikipedia, the free encyclopedia
"Gln" redirects here. For other uses, see GLN (disambiguation).
L-Glutamine
Skeletal formula of the L-isomer
Ball-and-stick model of the L-isomer as a zwitterion
IUPAC name[hide]
Glutamine
Other names[hide]
L-Glutamine
(levo)glutamide
2-Amino-4-carbamoylbutanoic acid
Identifiers
Abbreviations Gln, Q
CAS number 56-85-9 Yes
PubChem 738
ChemSpider 718 Yes
UNII 0RH81L854J Yes
EC-number 200-292-1
KEGG C00303 Yes
ChEBI CHEBI:28300 Yes
ChEMBL CHEMBL930
IUPHAR ligand 723
ATC code A16AA03
Jmol-3D images Image 1
SMILES
[show]
InChI
[show]
Properties[1]
Molecular formula C5H10N2O3
Molar mass 146.14 g mol−1
Melting point decomposes around 185°C
Solubility in water soluble
Chiral rotation [α]D +6.5ş (H2O, c = 2)
Supplementary data page
Structure and
properties n, εr, etc.
Thermodynamic
data Phase behaviour
Solid, liquid, gas
Spectral data UV, IR, NMR, MS
Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
(verify) (what is: Yes/?)
Infobox references
Glutamine (abbreviated as Gln or Q) is one of the 20 amino acids encoded by the standard genetic code. It is not recognized as an essential amino acid. Its side-chain is an amide formed by replacing the side-chain hydroxyl of glutamic acid with an amine functional group, making it the amide of glutamic acid. Its codons are CAA and CAG. In human blood, glutamine is the most abundant free amino acid, with a concentration of about 500–900 µmol/l.[2]
Contents [hide]
1 Structure
2 Functions
2.1 Producing and consuming organs
2.1.1 Producers
2.1.2 Consumers
2.2 Examples for the usage of glutamine
2.2.1 Aiding recovery after surgery
3 Nutrition
3.1 Occurrences in nature
3.1.1 Dietary sources
4 See also
5 References
6 External links
Structure[edit]
Glutamine zwitterionic forms at neutral pH: L-glutamine (left) and D-glutamine
Functions[edit]
Glutamine plays a role in a variety of biochemical functions:
Protein synthesis, as any other of the 20 proteinogenic amino acids
Regulation of acid-base balance in the kidney by producing ammonium[3]
Cellular energy, as a source, next to glucose[4]
Nitrogen donation for many anabolic processes, including the synthesis of purines[2]
Carbon donation, as a source, refilling the citric acid cycle[5]
Nontoxic transporter of ammonia in the blood circulation
Producing and consuming organs[edit]
Producers[edit]
Glutamine is synthesized by the enzyme glutamine synthetase from glutamate and ammonia. The most relevant glutamine-producing tissue is the muscle mass, accounting for about 90% of all glutamine synthesized. Glutamine is also released, in small amounts, by the lung and the brain.[6] Although the liver is capable of relevant glutamine synthesis, its role in glutamine metabolism is more regulatory than producing, since the liver takes up large amounts of glutamine derived from the gut.[2]
Consumers[edit]
The most eager consumers of glutamine are the cells of intestines,[2] the kidney cells for the acid-base balance, activated immune cells,[7] and many cancer cells.[5] In respect to the last point mentioned, different glutamine analogues, such as DON, Azaserine or Acivicin, are tested as anticancer drugs.
Examples for the usage of glutamine[edit]
In catabolic states of injury and illness, glutamine becomes conditionally essential (requiring intake from food or supplements).[8] Glutamine has been studied extensively over the past 10–15 years, and has been shown to be useful in treatment of injuries, trauma, burns, and treatment-related side effects of cancer, as well as in wound healing for postoperative patients. Glutamine is also marketed as a supplement used for muscle growth in weightlifting, bodybuilding, endurance, and other sports. Evidence indicates glutamine, when orally loaded, may increase plasma HGH levels by stimulating the anterior pituitary gland.[9] In biological research, L-glutamine is commonly added to the media in cell culture.[10][11] However, the high level of glutamine in the culture media may inhibit other amino acid transport activities.[12]
Aiding recovery after surgery[edit]
Glutamine is also known to have various side effects in reducing healing time after operations. Hospital-stay times after abdominal surgery can be reduced by providing parenteral nutrition regimens containing high amounts of glutamine to patients. Clinical trials have revealed patients on supplementation regimens containing glutamine have improved nitrogen balances, generation of cysteinyl-leukotrienes from polymorphonuclear neutrophil granulocytes, and improved lymphocyte recovery and intestinal permeability (in postoperative patients), in comparison to those that have no glutamine within their dietary regimen, all without any side effects.[13]
Nutrition[edit]
Occurrences in nature[edit]
Glutamine is the most abundant naturally occurring, nonessential amino acid in the human body, and one of the few amino acids that can directly cross the blood–brain barrier.[14] In the body, it is found circulating in the blood, as well as stored in the skeletal muscles. It becomes conditionally essential (requiring intake from food or supplements) in states of illness or injury.[8]
Dietary sources[edit]
Dietary sources of L-glutamine include beef, chicken, fish, eggs, milk, dairy products, wheat, cabbage, beets, beans, spinach, and parsley. Small amounts of free L-glutamine are also found in vegetable juices.[8]
See also[edit]
Isoglutamine
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