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allied

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Journal of Microbiology: Current Research | Volume 2

November 01-02, 2018 | London, UK

7

th

European

Clinical Microbiology Congress

4

th

International Conference on

Ophthalmology and Eye Disorder

Joint Event

&

Direct evidence of viral infection and mitochondrial alterations in the brain of fetuses at high risk for

schizophrenia

Segundo Mesa Castillo

Psychiatric Hospital of Havana, Cuba

T

here is increasingevidences that favor theprenatal beginning

of schizophrenia. Theseevidencespoint toward intra-uterine

environmental factors that act specifically during the second

pregnancy trimester producing a direct damage of the brain

of the fetus. The current available technology doesn’t allow

observing what is happening at cellular level since the human

brain is not exposed to a direct analysis in that stage of the life

in subjects at high risk of developing schizophrenia. Methods.

In 1977, we began a direct electron microscopic research of the

brain of fetuses at high risk from schizophrenicmothers in order

to finding differences at cellular level in relation to controls.

Results:

In these studies we have observed within the nuclei of

neurons thepresenceof completeand incomplete viral particles

that reacted in positive form with antibodies to herpes simplex

hominis type I [HSV1] virus and mitochondria alterations.

Conclusion:

The importance of these findings can have practical

applications in the prevention of the illness keeping in mind

its direct relation to the aetiology and physiopathology of

schizophrenia. A study of the gametes or the amniotic fluid

cells in women at risk of having a schizophrenic offspring

is considered. Of being observed the same alterations that

those observed previously in the cells of the brain of the

studied foetuses, it would intend to these women in risk of

having a schizophrenia descendant, previous information

of the results, the voluntary medical interruption of

the pregnancy or an early anti HSV1 viral treatment as

preventive measure of the later development of the illness

.

e:

segundo@infomed.sld.cu

Clinical Microbiology and Eye 2018, Volume 2

DOI: 10.4066/2591-8036-C1-003