TY - JOUR
T1 - Increased calcium influx through acetylcholine receptors in dunce neurons
AU - Alshuaib, Waleed B.
AU - Hasan, Mohamed
AU - Cherian, Susan P.
AU - Fahim, Mohamed A.
N1 - Funding Information:
Received 1 May 2003. This work was supported by Kuwait University Grant MPY02/00. Address correspondence to Dr. Waleed B. Alshuaib, Physiology Department, Faculty of Medicine, Kuwait University, P.O. Box 24923, Safat 13110, Kuwait. E-mail: [email protected]
PY - 2004/1
Y1 - 2004/1
N2 - Calcium homeostasis was studied in dunce, a Drosophila mutant that is defective in learning and memory. Fura 2-AM fluorescence photometry was used to measure the intracellular calcium concentration in wild type and dunce cleavage-arrested neurons under resting conditions and in response to neurotransmitters. After acetylcholine application, the peak [Ca 2+]i was greater in dunce (693 ± 125 nM) than in wild type neurons (464 ± 154 nM), but half decay time was shorter in dunce (66 ± 15 s) than in wild type neurons (104 ± 40 s). In contrast, the application of glutamate, NMDA, dopamine, and serotonin had no effect on [Ca2+]i. These results indicate that calcium influx through acetylcholine receptors is increased in dunce, compared to wild type neurons. The results also suggest that calcium extrusion to the outside and/or calcium buffering are enhanced in dunce, compared to wild type neurons. This disturbance in the homeostasis of cytosolic calcium concentration in dunce may be implicated in defective associative learning in Drosophila, and may play a role in acute and chronic neurodegenerative disorders in the mammalian brain.
AB - Calcium homeostasis was studied in dunce, a Drosophila mutant that is defective in learning and memory. Fura 2-AM fluorescence photometry was used to measure the intracellular calcium concentration in wild type and dunce cleavage-arrested neurons under resting conditions and in response to neurotransmitters. After acetylcholine application, the peak [Ca 2+]i was greater in dunce (693 ± 125 nM) than in wild type neurons (464 ± 154 nM), but half decay time was shorter in dunce (66 ± 15 s) than in wild type neurons (104 ± 40 s). In contrast, the application of glutamate, NMDA, dopamine, and serotonin had no effect on [Ca2+]i. These results indicate that calcium influx through acetylcholine receptors is increased in dunce, compared to wild type neurons. The results also suggest that calcium extrusion to the outside and/or calcium buffering are enhanced in dunce, compared to wild type neurons. This disturbance in the homeostasis of cytosolic calcium concentration in dunce may be implicated in defective associative learning in Drosophila, and may play a role in acute and chronic neurodegenerative disorders in the mammalian brain.
KW - Acetylcholine
KW - Calcium homeostasis
KW - Drosophila
KW - Dunce
KW - Fura 2-AM
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U2 - 10.1080/00207450490249392
DO - 10.1080/00207450490249392
M3 - Article
C2 - 14660074
AN - SCOPUS:0347761263
SN - 0020-7454
VL - 114
SP - 115
EP - 128
JO - International Journal of Neuroscience
JF - International Journal of Neuroscience
IS - 1
ER -