11C-Labeled Methionine Uptake in Gliomas: Modification after Therapy and Metabolic Correlations

Author(s):  
M.-C. Petit-Taboué ◽  
F. Dauphin ◽  
J.-M. Derlon
Keyword(s):  
1993 ◽  
Vol 17 (4) ◽  
pp. 660-661 ◽  
Author(s):  
Kazunari Ishii ◽  
Toshihide Ogawa ◽  
Jun Hatazawa ◽  
Iwao Kanno ◽  
Atsushi Inugami ◽  
...  

1982 ◽  
Vol 7 (5) ◽  
pp. 637-644 ◽  
Author(s):  
C. J. Cummins ◽  
R. A. Glover ◽  
O. Z. Sellinger
Keyword(s):  

1987 ◽  
Vol 252 (3) ◽  
pp. G320-G324
Author(s):  
P. Brachet ◽  
F. Alvarado ◽  
A. Puigserver

The kinetics of D- and L-methionine uptake by rings of everted intestine in vitro are consistent with a saturable Michaelis-Menten component (Km = 11.7 and 1.7 mM; Vmax = 0.53 and 0.74 mumol X g-1 X min-1 for D- and L-methionine, respectively) plus a linear, diffusional one. All the data could be fit with a diffusion constant (Kd = 3.2 microliters X g-1 X min-1), which was essentially the same, independent of whether it was estimated by iteration or by using the extracellular marker, inulin. Similar results were obtained from in vivo perfusion experiments, except that the diffusional term was negligible. D-Methionine was found to inhibit L-methionine uptake by intestinal rings according to fully noncompetitive kinetics (Ki = 45 mM). Another set of experiments with jejunal brush-border membrane vesicles showed that D-methionine uptake is dependent on a Na+ gradient and is significantly inhibited by L-methionine and L-proline, but not by beta-alanine and alpha-methylaminoisobutyric acid. Our results indicate that, in rat jejunum, D-methionine is taken up through a Na+-dependent pathway distinct from the neutral amino acid (L-methionine) carrier and from the imino acid (L-proline, alpha-methylaminoisobutyric acid, beta-alanine) carrier.


2001 ◽  
Vol 15 (4) ◽  
pp. 387-391 ◽  
Author(s):  
Atsuko Nagano-Saito ◽  
Takashi Kato ◽  
Toshihiko Wakabayashi ◽  
Masanari Nishino ◽  
Motonori Ohshima ◽  
...  

2007 ◽  
Vol 146 (1) ◽  
pp. 103-115 ◽  
Author(s):  
N. L. HEPBURN ◽  
C. H. KNIGHT ◽  
C. J. WILDE ◽  
K. A. K. HENDRY ◽  
H. GALBRAITH

SUMMARYL-methionine is a sulphur-containing nutritionally essential amino acid. It has a number of important roles in epidermal and dermal tissues of the integument of animals. Failure of normal function of these tissues in the hoof (claw) is a cause of lameness in cattle. Little is known about quantitative relationships between post-absorptive concentrations of nutrients including sulphur-containing amino acids and uptake and utilization by epidermis and dermis of the bovine claw. These parameters were studied at the tissue level by use of an established in vitro claw explant system using tissue from cattle of beef or dairy origin and L-[35S]-labelled methionine as tracer. The results showed that uptake of L-methionine by freshly prepared solear explants in Dulbecco's Modified Eagle Medium/F-12 Nutrient Mix (DMEM/F12) (1:1) medium containing 1·0 mmol L-methionine/litre was concentrative after 5–8 min, essentially linear for up to 10 min and became curvilinear thereafter. Maximum uptake and steady state conditions were obtained at approximately 30 min. Further measurements were made following 21 h incubation in culture medium. Under conditions of varying concentrations of L-methionine and measurement of uptake after 30 min, the presence of a saturable curve, that obeyed Michaelis–Menten kinetics, was demonstrated. Values of 3·61 mmol/litre and 5·84 mmol/kg intracellular water/30 min were obtained for KM and Vmax, respectively. Uptake was not influenced by L-cysteine and L-cystine concentrations in the culture media.Similar culture and incubation conditions were used in subsequent studies of DNA and protein synthesis. These showed that rates of incorporation of L-methionine into protein fractions and stimulation of DNA synthesis measured by methyl-thymidine incorporation were dependent on L-methionine concentrations in the medium. Maximal rates occurred at approximately 50 μmol/litre, which is in the normal physiological range, and at 1% of maximum uptake capacity. Examination of histological sections by autoradiography showed localization of L-[35S]-labelled methionine in basal and suprabasal epidermal cells with limited retention in dermis. Measurement, by a range of histological, immunohistochemical, electrophoretic, western blotting and autoradiographic techniques, provided further evidence of L-methionine-dependent regulation of proliferation, differentiation and synthesis of proteins under physiological concentrations, by epidermal horn-forming cells.A key role for L-methionine is suggested in the production of horn in bovine claw. The extrapolation of these in vitro data provides guidance for strategies to optimize methionine supply to claw tissues in vivo. Such extrapolation suggests the appropriateness of delivery of systemic concentrations of 50 μmol L-methionine/litre to maximize proliferative and protein depositional activity in solear epidermis and dermis in vivo.


Author(s):  
Katsuyoshi Mineura ◽  
Toshio Sasajima ◽  
Hiroyasu Sasajima ◽  
Masayoshi Kowada

2002 ◽  
Vol 16 (3) ◽  
pp. 207-211 ◽  
Author(s):  
Makoto Nakagawa ◽  
Yasuo Kuwabara ◽  
Masayuki Sasaki ◽  
Hirofumi Koga ◽  
Tao Chen ◽  
...  

1993 ◽  
Vol 264 (1) ◽  
pp. G30-G35 ◽  
Author(s):  
S. Hurst ◽  
S. M. Collins

We examined the ability of human recombinant interleukin-1 beta (hrIL-1 beta) to alter the release of [3H]norepinephrine ([3H]NE) by KCl or electrical field stimulation in longitudinal muscle-myenteric plexus of rat intestine. The cytokine had no immediate effect on either the basal or evoked release of [3H]NE. However, hrIL-1 beta caused a biphasic time-dependent suppression of evoked [3H]NE release that was delayed in onset. IL-1 beta also stimulated the cycloheximide-sensitive uptake of [35S] methionine uptake by the tissue. The initial suppression of [3H]NE release was observed after 30 min and could not be inhibited by cycloheximide. A delayed peak was observed after 120 min and was inhibited by cycloheximide. The effect of IL-1 beta was maximal at 10 ng/ml and could be prevented by a neutralizing anti-IL-1 beta antibody or by preincubating the tissue with an IL-1-receptor antagonist. These results indicate that IL-1 beta suppresses [3H]NE release from rat myenteric plexus by two mechanisms, one of which is independent of protein synthesis and the other of which is mediated by endogenous IL-1.


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