1.Effects of Pine Needle Butanol Fraction on Acetylcholine (ACh) and Its Related Enzymes in Brain of Rats.
Jin Ho CHOI ; Dae Ik KIM ; Si Hyang PARK ; Nam Ju KIM ; Seung Jin BAEK ; Koon Ja KIM ; Hyun Sook KIM
The Korean Journal of Nutrition 2004;37(3):176-181
This study was designed to investigate the effects of buthanol (BuOH) fraction of pine (Pinus densiflora Sieb et Zucc) needle on cholesterol and lipofuscin (LF) accumulations, acetylcholine (ACh) and its related enzyme activities such as choline acetyltransferase (CAhT) and acetylcholinesterase (AChE), and monoamone oxidase-B (MAO-B) activity, which destroyed the catecholamine-related neurotransmitters in brain membranes of Sprague-Dawley (SD) rats. Male SD rats were fed basic diets (control group) or experimental diets (BuOH-25, BuOH-50 and BuOH-100) for 45 days. Cholesterol accumulations in mitochondria and microsomes were significantly inhibited (about 14 - 17% and 23 - 34%, respectvely) in BuOH-50 and BuOH-100 groups, whereas LF levels were significantly inhibited (about 10 - 14%) in BuOH-50 and BuOH-100 groups compared with control group. ACh levels and ChAT activities were significantly increased (about 11 - 17% and 11 - 23%, respectively) in membranes of BuOH-50 and BuOH-100 groups compared with control group. AChE activities were significantly increased (about 14 - 17%) in membranes of BuOH-50 and BuOH-100 groups. There was no significant difference in MAO-B activities between control and experimental diet groups. The results suggest that butanol fraction of pine needle may play an effective role in an antiaging effect and improving a learning and memory impairments.
Acetylcholine*
;
Acetylcholinesterase
;
Animals
;
Brain*
;
Cholesterol
;
Choline O-Acetyltransferase
;
Diet
;
Humans
;
Learning
;
Lipofuscin
;
Male
;
Membranes
;
Memory
;
Microsomes
;
Mitochondria
;
Monoamine Oxidase
;
Needles*
;
Neurotransmitter Agents
;
Rats*
;
Rats, Sprague-Dawley
2.Effects of Pine Needle Ethyl Acetate Fraction on Acetylcholine(ACh) and Its Related Enzymes in Brain of Rats.
Jin Ho CHOI ; Dae Ik KIM ; Si Hyang PARK ; Seung Jin BAEK ; Nam Ju KIM ; Weon Ki CHO ; Koon Ja KIM ; Hyun Sook KIM
The Korean Journal of Nutrition 2004;37(2):95-99
This study was designed to investigate the effects of ethyl acetate (EtOAc) fraction of pine (Pinus densiflora Sieb et Zucc) needle on cholesterol and lipofuscin (LF) accumulations, acetylcholine (ACh) and its related enzyme activities such as choline acetyltransferase (ChAT) and acetylcholinesterase (AChE), and monoamine oxidase-B (MAO-B) activity, which destroyed the catecholamine related neurotransmitters in brain membranes of Sprague- Dawley (SD) rats. Male SD rats were fed basic diets (control group) and experimental diets (EtOAc-25, EtOAc-50 and EtOAc-100) for 45 days. Cholesterol accumulations in mitochondria and microsomes were significantly inhibited (11.8 - 12.1% and 9.6 - 13.0%, respectvely) in EtOAc-50 and EtOAc-100 groups. ACh levels and ChAT activities were significantly increased about 10% in membranes of EtOAc-100 group compared with control group. AChE activities were significantly increased about 8 - 12% in membranes of EtOAc-50 and EtOAc-100 groups compared with control group. MAO-B activities were significantly inhibited about 10% in membrane of EtOAc-100 group compared with control group. These results suggest that ethyl acetate fraction of pine needle may play an effective role in inhibiting cholesterol and improving a membrane fluidity, and learning and memory impairments.
Acetylcholine
;
Acetylcholinesterase
;
Animals
;
Brain*
;
Cholesterol
;
Choline O-Acetyltransferase
;
Diet
;
Humans
;
Learning
;
Lipofuscin
;
Male
;
Membrane Fluidity
;
Membranes
;
Memory
;
Microsomes
;
Mitochondria
;
Monoamine Oxidase
;
Needles*
;
Neurotransmitter Agents
;
Rats*
3.CD4+T lymphocyte, beta2-microglobulin and p24 antigen level in HIV infected persons.
Yung Kul CHO ; Byung Sun CHO ; Yung Bong KIM ; Koon Je CHO ; Choon KANG ; Sung Soon KIM ; Mi Kyung KI ; Sook Jin HUH ; Tae Sook KIM ; Yang Ja CHO ; Yung Oh SHIN
Korean Journal of Infectious Diseases 1993;25(2):139-149
No abstract available.
HIV*
;
Humans
;
Lymphocytes*