Title of article :
Evaluation of Rat Brain Morphology Following the Induction of Acute Meningitis Treated with Ceftriaxone
Author/Authors :
Agarkova, A. A Belgorod State University - Belgorod - Pobeda, Russia , Tverskoi, A. V Belgorod State University - Belgorod - Pobeda, Russia , Morozov, V. N Belgorod State University - Belgorod - Pobeda, Russia , Tverskaya, A. V Belgorod State University - Belgorod - Pobeda, Russia , Morozova, E. N Belgorod State University - Belgorod - Pobeda, Russia , Mukhina, T. S Belgorod State University - Belgorod - Pobeda, Russia
Abstract :
The soft and delicate tissue of the brain, which is the center of our coordination, is protected by its surrounding
layers. The disruption of these layers results in complicated situations and serious health problems. The brain
has three protective layers of bone or skull tissue, the blood tissue layer, and finally the meningeal layer. The
layer of blood tissue contains the blood vessels that are located between the skull and the meningeal membranes.
If germs or foreign matter enter the fluid through the blood vessels under any circumstances and cause infection,
the bones that protect the meninges will break and cause tissue damage. The present study aimed to assess the
histological and immunohistochemical characteristics of the brain of rats that underwent induced acute purulent
pneumococcal meningitis after antibiotic therapy with Ceftriaxone. A number of 20 white adult male Wistar rats
were assigned to three groups. The first group (n=5) regarded as the control were injected with a saline solution
into the subarachnoid space in an equivalent amount. The second and third groups of rats (n=5 and 10,
respectively) were infected with acute purulent meningitis by the injection of 10 μl of Streptococcus
pneumoniae (S. pneumonia) suspension into the subarachnoid space of the brain using a 23-G needle. The
various areas of the brains of rats after meningitis induced by S. pneumoniae were examined after the treatment
with Ceftriaxone. The S. pneumoniae culture was injected into the subarachnoid space in the area of the
rhomboid fossa. Treatment started 18 h after the injection. On day 10, a repeated puncture was performed with
the analysis of cerebrospinal fluid in order to confirm the absence of meningitis; thereafter, the animals were
taken out of the experiment. No signs of meningitis were found on histological examination. Mild perivascular
and pericellular focal edema were revealed with signs of overload of the lymphatic system in the brain and focal
ischemic changes in neurons. The investigation of expression with caspase-3 revealed a positive reaction of
individual neurons. A positive reaction with antibodies to NeuN and Doublecortin was detected in most
neurons; moreover, Glial fibrillary acidic protein (GFAP)-positive astrocytes and their processes were visualized
in all layers of the brain substance. The reaction with neuron-specific enolase (NSE), microtubule-associated
protein 2 (MAP-2), CD 31, and CD 34 was negative. Typical structure and pictures pointed to an intact brain
and purulent meningitis in the first and second groups. The microscopic image and the changes revealed during
immunohistochemistry by dual corticosteroid antibodies and neuronal nuclear protein were characterized by
predominantly cytoplasmic and perinuclear reactions, respectively. Some neurons are positive for caspase-3 and
are related to changes in the characteristic of premature aging.
Keywords :
Brain of rats , Immunohistochemical markers , Ceftriaxone , Acute meningitis
Journal title :
Archives of Razi Institute