ANimal cells

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Morphological growth and development has occurred by factors affect the cells properties. These variations are take place by changing on cells functional characters which cause morphological growth, development and age related deviations. Accordingly, based on scientific researches and analyzing the scientific experiments, it is had been summarized that effects of morphological changes form to malignant cells. There has been wide scientific research based on morphological development of distributions affect functional development. In 1996 Sharon Freeman, Lily Cherny and Haim Sohmer published a paper titled “Thyroxine affect physiological and morphological development of the ear” discussing theories about the development of distortion product otoacoustic emissions (DPE) which represented cochlear amplifier activity in hyperthyroid. In hearing research, scientist compared onset and development of auditory nerve-brainstem evoked responses representing overall cochlear function and to morphological development of the ear. (1) For this research, rats had been divided in neonatal hyperthyroid (n=10) and control group (n=10) rat. These rats had been compared based on responses of the development of auditory nerve-brainstem and bone-conducted responses. Distortion product otoacoustic emissions (DPE) had been recorded at earlier high (8 kHz) and low (3 kHz). At the end of the hearing research, it is stated that results of the morphological comparison, there was a consistent difference between level of development of the outer and middle ears. As a result, Thyroxine-injected rats had been showed clear signs of neonatal hyperthyroidism of the cochlea such as distortion product otoacoustic emissions. (1) Similarly, scientist R.P Birth an... ... middle of paper ... ...al findings suggest that prenatal exposure to Zeranol or DES induces abnormal testicular diffentiation in the mouse.” (4) The last experiment is to understand the neurodegenerative disease. In 1996, M. Barkats analyzed the granule cell number in dentate gyrus which had been reported to vary among inbred strains of mice. Scientists were hypothesizing about age-related changes in morphological of dentate gyrus both in animals and humans. Therefore the purpose of this experiment was to study “investigate for strain difference in hippocampal structure changes in old C57BL/6J (B) and DBA/2J (D) mice as compared with younger ones.” (5) At the end of the experiment Barkats concluded examined in hippocampus on mouse strains showed neuroanatomical parameters always reduced with age and granule cell population in dentate gyrus could be influenced by some hereditary factors.

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