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Ruth Simeon and Nick
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Objective Introduction These signals depend on a sodium-calcium gradient (created by a Na+-Ca++ exchange pump) and calcium channels (Bellairs and Osmond, 1998). In addition, other signaling molecules, such as acetylcholine and norinephrine can affect embryonic hearts (Gilbert, 2003). Due to the importance of the circulatory system, morphological changes caused by signals and external chemicals, such as caffeine, have the potential to cause irreversible harm on a developing embryo. Caffeine is a trimethylxanthine
(Gwinn, 1992) and a teratogen, which is an agent responsible
for developmental abnormalities (Braun, 1996). Caffeine also
increases the teratogenic effects of ephedrine on embryonic
chick hearts (Nishikawa, 1985). Although it is not known
exactly how caffeine affects an embryo on a molecular level,
they have not yet developed the succession of liver enzymes
present in adults that are needed to degrade caffeine
(Braun, 1996). Figure 1. A three-day-old chick
embryo, with visible circulatory system and
somites. Figure 2. A four-day chick
embryo. |