Literature DB >> 10620659

Low cerebral glucose extraction rates in the human medial temporal cortex and cerebellum.

S Sakamoto1, K Ishii.   

Abstract

Previous studies have reported that there exist different regional sensitivities to acute hypoxia. To better understand these differences, we estimated regional differences of cerebral blood flow (CBF), cerebral glucose metabolism (CMRglc) and kinetic constants (K(1), k(2), k(3)) in the human cortex under resting conditions. CBF, CMRglc, kinetic rate constants and glucose extraction rate (GER) were measured in eight normal male subjects (mean age: 26.1+/- 4.9 years) using the 15O-water autoradiographic technique and subsequently the dynamic and the static [18F]2-fluoro-2-deoxy-D-glucose technique with positron emission tomography (PET). Of all the brain structures investigated, the medial temporal lobe showed the lowest CBF (46.0 ml/100 g/min) and lowest CMRglc (3.97 mg/100 g/min). The medial temporal GER was lowest (8.9%), followed by the cerebellar GER (9.3%). While the cerebellar blood flow (64.0 ml/100 g/min) was the highest, the cerebellar metabolic rate for glucose (5.79 mg/100 g/min) was relatively low. The cerebellum showed the highest K(1) value (0.13) and k(2) value (0.16), and the lowest k(3) value (0.05). In the medial temporal cortices and cerebellum, CMRglc and GER were lower than those in the neocortices. These results indicate that there are great perfusional/metabolic differences between the medial temporal lobe, cerebellum and other brain regions in the normal human brain under resting conditions.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 10620659     DOI: 10.1016/s0022-510x(99)00286-5

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  6 in total

1.  Volumetric analysis of regional cerebral development in preterm children.

Authors:  Shelli R Kesler; Laura R Ment; Betty Vohr; Sarah K Pajot; Karen C Schneider; Karol H Katz; Timothy B Ebbitt; Charles C Duncan; Robert W Makuch; Allan L Reiss
Journal:  Pediatr Neurol       Date:  2004-11       Impact factor: 3.372

2.  Functional genomics of brain aging and Alzheimer's disease: focus on selective neuronal vulnerability.

Authors:  Xinkun Wang; Mary L Michaelis; Elias K Michaelis
Journal:  Curr Genomics       Date:  2010-12       Impact factor: 2.236

3.  Aging and gene expression in the primate brain.

Authors:  Hunter B Fraser; Philipp Khaitovich; Joshua B Plotkin; Svante Pääbo; Michael B Eisen
Journal:  PLoS Biol       Date:  2005-08-02       Impact factor: 8.029

4.  A statistical investigation of normal regional intra-subject heterogeneity of brain metabolism and perfusion by F-18 FDG and O-15 H2O PET imaging.

Authors:  Ching-yee Oliver Wong; Joseph Thie; Marianne Gaskill; Richard Ponto; Jack Hill; Hai-yan Tian; Helena Balon; Dafang Wu; Darlene Fink-Bennett; Conrad Nagle
Journal:  BMC Nucl Med       Date:  2006-07-12

5.  The cerebellum ages slowly according to the epigenetic clock.

Authors:  Steve Horvath; Vei Mah; Ake T Lu; Jennifer S Woo; Oi-Wa Choi; Anna J Jasinska; José A Riancho; Spencer Tung; Natalie S Coles; Jonathan Braun; Harry V Vinters; L Stephen Coles
Journal:  Aging (Albany NY)       Date:  2015-05       Impact factor: 5.682

6.  Direct comparison study between FDG-PET and IMP-SPECT for diagnosing Alzheimer's disease using 3D-SSP analysis in the same patients.

Authors:  Takashi Nihashi; Hiroshi Yatsuya; Kazumasa Hayasaka; Rikio Kato; Shoji Kawatsu; Yutaka Arahata; Katsushige Iwai; Akinori Takeda; Yukihiko Washimi; Kumiko Yoshimura; Kanako Mizuno; Takashi Kato; Shinji Naganawa; Kengo Ito
Journal:  Radiat Med       Date:  2007-07-27
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.