Cerebrum Samples Research Articles

The potential use of skin and liver as biomarkers to estimate mercury in the brain, kidney, and muscle of bottlenose dolphins (Tursiops truncatus)

For marine cetaceans, Hg biomagnification can negatively affect neurological, hepatic, renal, and immune functions. To evaluate the use of biomarkers for Hg in dolphins, multiple tissues were analyzed from 127 stranded common bottlenose dolphins (Tursiops truncatus) from the estuarine and oceanic waters of Virginia, USA. Twenty-two percent of liver Hg concentrations exceeded the published observed effect level for liver abnormalities, and 26 % of cerebrum samples exceeded the published threshold for neurochemical changes, suggesting that Hg may have impacted dolphin health. Mercury tissue levels were similar to or lower than those reported from other locations (liver range: 1.4–943 μg/g-dw). Significant correlations were found between tissue types, indicating that skin or liver can be used as a biomarker to estimate the total Hg concentrations in the other tissue types (kidney, liver, cerebrum, cerebellum, pons). This is the first study to measure Hg concentrations in multiple brain regions of T. truncatus.

Identification of compound causing yellow bone discoloration following alpha-glycosyl isoquercitrin exposure in Sprague\u2013Dawley rats

Previous rat toxicity studies of alpha-glycosyl isoquercitrin (AGIQ), a water-soluble flavonol glycoside derived from rutin, revealed systemic yellow bone discoloration. This investigative study was conducted to determine the AGIQ metabolite(s) responsible for the discoloration. Female Sprague–Dawley rats were administered dietary AGIQ at doses of 0%, 1.5%, 3.0%, or 5.0% (0, 1735.0, 3480.8, and 5873.7 mg/kg/day, respectively) for 14 days, followed by a 14- or 28-day recovery period. Measurements of quercetin in urine and quercetin, quercetin 3-O-glucuronide, kaempferol, and 3-o-methylquercetin metabolites of AGIQ in bone (femur), white and brown fat, and cerebrum samples were conducted following the exposure period and each recovery period. Gross examination of the femur revealed yellow discoloration that increased in intensity with dose and was still present in a dose-related manner following both recovery periods. Quercetin, at levels correlating with AGIQ dose, was measured in the urine following the 14-day exposure period and, at lower concentrations, 14 or 28 days following cessation of AGIQ exposure. All four metabolites were present in a dose-dependent manner in the femur following 14 days of dietary exposure; only quercetin, quercetin 3-O-glucuronide, and 3-o-methylquercetin were present during the recovery periods. Quercetin, quercetin 3-O-glucuronide, and 3-o-methylquercetin were detected in white fat (along with kaempferol), brown fat (excluding quercetin due to analytical interference), and cerebrum samples, indicating systemic availability of the metabolites. Collectively, these data implicate quercetin, quercetin 3-O-glucuronide, or 3-o-methylquercetin (or a combination thereof) as the most likely metabolite of AGIQ causing the yellow discoloration of bone in rats administered dietary AGIQ.

Morphometric analysis of the arteries of Willis Polygon

Abstract Objective: Willis polygon forms the basis of the arterial circulation of the cerebrum. Willis polygon is a vascular structure whom variations are not rare. Knowledge of the anatomy and preservation of its integrity is crucial for performing neurovascular surgery and intracranial tumour surgery. Because of the important vascular and neurological structures, approaches to this region are considered extremely risky. One of the main variations in-person basis is the diameter differences of the arteries, which forms Willis polygon, between the left and right hemispheres. About structure and variations, studies of Rhoton and Yasargil had formed the touchstone. Our aim is to contribute to the literature and clinical studies, to be done in the future, by comparing our results with previous studies about variations and morphometric features of Willis polygon. Methods: Arteries of 30 fresh cadaver brains were examined during autopsies in T.C. Ministry of Justice Istanbul Forensic Science Institute. Bilaterally anterior cerebral artery A1 segment lengths, distance between anterior communicating artery-callosomarginal artery outputs, posterior cerebral artery P1 segment lengths were measured using a digital calliper. After dissections and measures, photos of the region were taken and vascular anatomy and variations noted. From every single cerebrum samples were obtained from bilaterally A1, A2, callosomarginal artery, middle cerebral artery, posterior communicant artery, P1 and basilar artery. Samples were fixed by using 10% buffered-formalin. Taken samples were transported to Marmara University Faculty of Medicine, Department of Anatomy Laboratory. Samples were examined and interior diameters were measured under the microscope. Results: Our results with artery diameters and lengths were similar with literature. Different from literature, in anterior cerebral artery A1 segment, posterior cerebral artery P1 segment and posterior communicant artery no aplasia were noted. In 50% of the samples, callosomarginal artery were originate from A2 segment. In one case, we observed left and right pericallosal arteries were joined together at the end of the A2 segment and continued as a single pericallosal artery. We could not find any information about this variation in the literature. Conclusion: Before surgical operations, detailed knowledge of Willis polygon and evaluation of the pre-op cerebral angiography considering possible variations, reduce mortality and morbidity ratios. In addition, because of the role of flow gradients of Willis polygon in aneurysm formation, and in terms of better understanding the collateral circulation which is important in vascular occlusive diseases and vascular surgery, we believe, more anatomic studies about this region needed.

Toxoplasma gondii in stranded marine mammals from the North Sea and Eastern Atlantic Ocean: Findings and diagnostic difficulties

The occurrence of the zoonotic protozoan parasite Toxoplasma gondii in marine mammals remains a poorly understood phenomenon. In this study, samples from 589 marine mammal species and 34 European otters (Lutra lutra), stranded on the coasts of Scotland, Belgium, France, The Netherlands and Germany, were tested for the presence of T. gondii. Brain samples were analysed by polymerase chain reaction (PCR) for detection of parasite DNA. Blood and muscle fluid samples were tested for specific antibodies using a modified agglutination test (MAT), a commercial multi-species enzyme-linked immunosorbent assay (ELISA) and an immunofluorescence assay (IFA). Out of 193 animals tested by PCR, only two harbour porpoise (Phocoena phocoena) cerebrum samples, obtained from animals stranded on the Dutch coast, tested positive. The serological results showed a wide variation depending on the test used. Using a cut-off value of 1/40 dilution in MAT, 141 out of 292 animals (41%) were positive. Using IFA, 30 out of 244 tested samples (12%) were positive at a 1/50 dilution. The commercial ELISA yielded 7% positives with a cut-off of the sample-to-positive (S/P) ratio≥50; and 12% when the cut-off was set at S/P ratio≥20. The high number of positives in MAT may be an overestimation due to the high degree of haemolysis of the samples and/or the presence of lipids. The ELISA results could be an underestimation due to the use of a multispecies conjugate. Our results confirm the presence of T. gondii in marine mammals in The Netherlands and show exposure to the parasite in both the North Sea and the Eastern Atlantic Ocean. We also highlight the limitations of the tests used to diagnose T. gondii in stranded marine mammals.

Caracterização imuno-histoquímica das alterações encefálicas em bovinos com hepatopatia tóxica por Senecio sp

Intoxicação por Senecio spp. é causa importante de doença e morte em bovinos no Rio Grande do Sul e frequentemente cursa com manifestações clínicas neurológicas e alterações histológicas encefálicas. Foi efetuada avaliação histológica em fígado e encéfalo de dez bovinos naturalmente intoxicados por Senecio sp. e foram realizadas as técnicas de histoquímica de ácido periódico de Schiff e de imuno-histoquímica, com emprego dos anticorpos anti-proteína fibrilar ácida (GFAP), anti-proteína S100 e anti-vimentina em amostras de telencéfalo, tronco encefálico e cerebelo. Na histologia do SNC observou-se vacuolização discreta a acentuada em substância branca e/ou junção entre substância branca e cinzenta, caracterizada como degeneração esponjosa. Na avaliação histoquímica e imuno-histoquímica não houve diferenças significativas em relação aos achados em encéfalo de onze bovinos controle, adultos, sem alterações hepáticas e/ou encefálicas, avaliados pelas mesmas técnicas.

Effect of dietary fat and cholesterol level on tissue cholesterol concentrations of growing pigs selected for high or low serum cholesterol.

Thirty-six female pigs selected for three generations for high or low serum cholesterol were chosen to evaluate the effects of a high-fat, high-cholesterol diet and a low-fat, low-cholesterol diet provided on an ad libitum basis for 92 d beginning at 12 wk of age on the cholesterol content and percentage of fat in muscle and organ tissues. The pigs were four-way crosses (Chester White x Landrace x Large White x Yorkshire). Samples of cerebrum, heart, ileum, kidney, liver, longissimus muscle, semitendinosus muscle, and subcutaneous fat were collected from each animal for determination of cholesterol concentration. The liver was the only tissue that had a significant difference in cholesterol content and in fat percentage between the genetic groups (high serum cholesterol and low serum cholesterol) and between the two diets (high-fat, high-cholesterol diet and low-fat, low-cholesterol diet). There were no interactions between diet and genetic background on cholesterol accretion or on the percentage of fat in the tissues.

Melanotropic-lipolytic peptides in various regions of bovine, simian and human brains and in simian and human cerebrospinal fluids.

Acetic acid extracts of lyophilized samples of cerebrum, cerebellum, and various midbrain and hindbrain regions of bovine, simian and human brain cause darkening of the frog’s skin (melanotropic action) and release of free fatty acids from the rabbit's adipose tissue (lipolytic action). The melanotropic potencies of the regions of bovine brain vary according to the order: posterior pituitary gland 7900 / anterior pituitary gland 950 / hypothalamus 450 / choroid plexus 270 / pineal gland 200 / epithalamus 65 / area postrema 60 / subcommissural organ 30 / thalamus 20 / caudate nucleus 15 / cerebellum 10 / corpus callosum 2 / substantia nigra 2 / cerebral cortex 2 / medulla 2 / pyriform—amygdaloid 2 / midbrain 1 / septum pellucidum 1 / hippocampus 1 / pons 1. Lipolytic potencies of the regions vary in the same manner. The distribution of melanotropic and lipolytic activities in simian and human central nervous systems was similar to that in the bovine. Both biologic activities in extracts of all regions were...