TY - JOUR
T1 - Brain neurotransmitter profile is deranged during sepsis and septic encephalopathy in the rat
AU - Freund, Herbert R.
AU - Muggia-Sullam, Michael
AU - Peiser, Jochanan
AU - Melamed, Eldad
N1 - Funding Information:
’ Supported in part by grants from the Joint Research Fund of the Hebrew University-Hadassah Medical school and the Max Bogen Fund. The technical assktance of A. Avinezer, Y. Rosenthal, and B. Zelikovitz is greatly appreciated.
PY - 1985/1/1
Y1 - 1985/1/1
N2 - Patients with sepsis often manifest symptoms of encephalopathy similar to those observed in portasystemic encephalopathy. As a causal relationship has been demonstrated between hepatic encephalopathy and a deranged brain neurotransmitter profile, the catecholaminergic and serotoninergic brain neurotransmitter profile in a septic rat model was investigated. Septic animals exhibited lower levels of norepinephrine (NE), 3,4-dihydroxyphenylacetic acid, and homovanillic acid compared to normal controls. Severely septic animals with encephalopathy exhibited significantly lower levels of NE, dopamine, 5-hydroxytryptamine, and 5-hydroxyindoleacetic acid compared to rats only mildly septic with no encephalopathy. The infusion of branched chain amino acids during sepsis had no effect on this deranged brain neurotransmitter profile. Previous results of derangements in the blood-brain barrier transport mechanism combined with the present findings of a deranged brain amino acid and neurotransmitter profile during sepsis may be responsible, at least in part, for the metabolic encephalopathy observed during sepsis and might suggest a common etiology for septic, hepatic, and other metabolic encephalopathies.
AB - Patients with sepsis often manifest symptoms of encephalopathy similar to those observed in portasystemic encephalopathy. As a causal relationship has been demonstrated between hepatic encephalopathy and a deranged brain neurotransmitter profile, the catecholaminergic and serotoninergic brain neurotransmitter profile in a septic rat model was investigated. Septic animals exhibited lower levels of norepinephrine (NE), 3,4-dihydroxyphenylacetic acid, and homovanillic acid compared to normal controls. Severely septic animals with encephalopathy exhibited significantly lower levels of NE, dopamine, 5-hydroxytryptamine, and 5-hydroxyindoleacetic acid compared to rats only mildly septic with no encephalopathy. The infusion of branched chain amino acids during sepsis had no effect on this deranged brain neurotransmitter profile. Previous results of derangements in the blood-brain barrier transport mechanism combined with the present findings of a deranged brain amino acid and neurotransmitter profile during sepsis may be responsible, at least in part, for the metabolic encephalopathy observed during sepsis and might suggest a common etiology for septic, hepatic, and other metabolic encephalopathies.
UR - http://www.scopus.com/inward/record.url?scp=0021987310&partnerID=8YFLogxK
U2 - 10.1016/0022-4804(85)90037-X
DO - 10.1016/0022-4804(85)90037-X
M3 - Article
C2 - 2858604
AN - SCOPUS:0021987310
SN - 0022-4804
VL - 38
SP - 267
EP - 271
JO - Journal of Surgical Research
JF - Journal of Surgical Research
IS - 3
ER -