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1.
J Ethnopharmacol ; 195: 159-165, 2017 Jan 04.
Article in English | MEDLINE | ID: mdl-27825990

ABSTRACT

ETHNOPHARMACOLOGICAL RELEVANCE: The development of compounds able to improve metabolic syndrome and mitigate complications caused by inappropriate glycemic control in type 1 diabetes mellitus is challenging. The medicinal plant with established hypoglycemic properties Garcinia kola Heckel might have the potential to mitigate diabetes mellitus metabolic syndrome and complications. AIM OF THE STUDY: We have investigated the neuroprotective properties of a suspension of G. kola seeds in long-term type 1 diabetes mellitus rat model. MATERIALS AND METHODS: Wistar rats, made diabetic by single injection of streptozotocin were monitored for 8 months. Then, they were administered with distilled water or G. kola oral aqueous suspension daily for 30 days. Body weight and glycemia were determined before and after treatment. After sacrifice, cerebella were dissected out and processed for stereological quantification of Purkinje cells. Histopathological and immunohistochemical analyses of markers of neuroinflammation and neurodegeneration were performed. RESULTS: Purkinje cell counts were significantly increased, and histopathological signs of apoptosis and neuroinflammation decreased, in diabetic animals treated with G. kola compared to diabetic rats given distilled water. Glycemia was also markedly improved and body weight restored to non-diabetic control values, following G. kola treatment. CONCLUSIONS: These results suggest that G. kola treatment improved the general condition of long-term diabetic rats and protected Purkinje cells partly by improving the systemic glycemia and mitigating neuroinflammation.


Subject(s)
Cerebellar Diseases/prevention & control , Cerebellum/drug effects , Diabetes Mellitus, Experimental/drug therapy , Diabetes Mellitus, Type 1/drug therapy , Diabetic Neuropathies/prevention & control , Garcinia kola/chemistry , Hypoglycemic Agents/pharmacology , Nerve Degeneration , Neuroprotective Agents/pharmacology , Plant Preparations/pharmacology , Animals , Apoptosis/drug effects , Blood Glucose/drug effects , Blood Glucose/metabolism , Cerebellar Diseases/blood , Cerebellar Diseases/etiology , Cerebellar Diseases/pathology , Cerebellum/metabolism , Cerebellum/pathology , Diabetes Mellitus, Experimental/blood , Diabetes Mellitus, Experimental/chemically induced , Diabetes Mellitus, Type 1/blood , Diabetes Mellitus, Type 1/chemically induced , Diabetic Neuropathies/blood , Diabetic Neuropathies/etiology , Diabetic Neuropathies/pathology , Hypoglycemic Agents/isolation & purification , Neuroimmunomodulation/drug effects , Neuroprotective Agents/isolation & purification , Phytotherapy , Plant Preparations/isolation & purification , Plants, Medicinal , Purkinje Cells/drug effects , Purkinje Cells/metabolism , Purkinje Cells/pathology , Rats, Wistar , Streptozocin , Time Factors , Tumor Necrosis Factor-alpha/metabolism , fas Receptor/metabolism
2.
Int J Radiat Biol ; 92(10): 590-5, 2016 10.
Article in English | MEDLINE | ID: mdl-27442260

ABSTRACT

PURPOSE: Adverse effects on human health caused by electromagnetic fields (EMF) associated with the use of mobile phones, particularly among young people, are increasing all the time. The potential deleterious effects of EMF exposure resulting from mobile phones being used in close proximity to the brain require particular evaluation. However, only a limited number of studies have investigated the effects of prenatal exposure to EMF in the development of the pyramidal cells using melatonin (MEL) and omega-3 (ω-3). MATERIALS AND METHODS: We established seven groups of pregnant rats consisting of three animals each; control (CONT), SHAM, EMF, EMF + MEL, MEL, EMF + ω-3 and ω-3 alone. The rats in the EMF, EMF + MEL, EMF + ω-3 groups were exposed to 900 MHz EMF for 60 min/day in an exposure tube during the gestation period. The CONT, MEL and ω-3 group rats were not placed inside the exposure tube or exposed to EMF during the study period. After delivery, only spontaneously delivered male rat pups were selected for the establishment of further groups. Each group of offspring consisted of six animals. The optical fractionator technique was used to determine total pyramidal neuron numbers in the rat hippocampal region. RESULTS: The total number of pyramidal cells in the cornu ammonis (CA) in the EMF group was significantly lower than in the CONT, SHAM, EMF + MEL, and EMF + ω-3 groups. No significant difference was observed between the EMF, MEL and ω-3 groups. No difference was also observed between any groups in terms of rats' body or brain weights. CONCLUSION: MEL and ω-3 can protect the cell against neuronal damage in the hippocampus induced by 900 MHz EMF. However, further studies are now needed to evaluate the chronic effects of 900 MHz EMF on the brain in the prenatal period.


Subject(s)
Electromagnetic Fields/adverse effects , Fatty Acids, Omega-3/administration & dosage , Hippocampus/pathology , Hippocampus/radiation effects , Melatonin/administration & dosage , Prenatal Exposure Delayed Effects/pathology , Prenatal Exposure Delayed Effects/prevention & control , Animals , Dose-Response Relationship, Drug , Dose-Response Relationship, Radiation , Female , Hippocampus/drug effects , Male , Microwaves/adverse effects , Neurons/drug effects , Neurons/pathology , Neurons/radiation effects , Neuroprotective Agents/administration & dosage , Pregnancy , Prenatal Exposure Delayed Effects/etiology , Radiation Dosage , Radiation-Protective Agents/administration & dosage , Rats , Rats, Wistar
3.
J Chem Neuroanat ; 75(Pt B): 52-61, 2016 09.
Article in English | MEDLINE | ID: mdl-26686296

ABSTRACT

Rapid advances in technology involve increased exposures to radio-frequency/microwave radiation from mobile phones and other wireless transmitting devices. As cell phones are held close to the head during talking and often stored next to the reproductive organs, studies are mostly focused on the brain. In fact, more research is especially needed to investigate electromagnetic field (EMF)'s effects on the central nervous system (CNS). Several studies clearly demonstrate that EMF emitted by cell phones could affect a range of body systems and functions. Recent work has demonstrated that EMF inhibit the formation and differentiation of neural stem cells during embryonic development and also affect reproductive and neurological health of adults that have undergone prenatal exposure. The aim of this review is to discuss the developing CNS and explain potential impacts of EMF on this system.


Subject(s)
Brain/growth & development , Brain/radiation effects , Cell Phone , Electromagnetic Fields/adverse effects , Animals , Cell Phone/trends , Humans , Neurogenesis/physiology , Neurogenesis/radiation effects
4.
Ren Fail ; 37(8): 1379-83, 2015.
Article in English | MEDLINE | ID: mdl-26365794

ABSTRACT

OBJECTIVE: In this study, we aimed to investigate the effect of diclofenac sodium (DS) and melatonin (MEL) on kidney of the prenatally administered rats. MATERIALS AND METHODS: Pregnant rats were divided into the control, physiological saline, DS, and DS + MEL groups. All injections were given beginning from the 5th day after mating to the 15th day of the pregnancy. Physical dissector and Cavalieri principle were used to estimate the numerical density and total number of glomeruli and the volumetric parameters of kidney, respectively. RESULTS: Our stereological results indicated that DS application during the pregnancy lead to decrease in the mean volume, numerical density, and total number of the glomeruli (p < 0.05). In addition, we determined that usage of the MEL with the DS caused increases in the mean volume, numerical density, and total number of the glomeruli (p < 0.05). So, there was no significant difference in terms of the any parameter between the CONT and DS + MEL groups (p > 0.05). Light microscopic investigation showed congestion in blood vessels and shrinkage of the Bowman's space in the DS group. Moreover, there was degeneration in nephrons including glomerulosclerosis and tubular defects, and an increase in the connective tissue in the kidneys of the DS-treated group. However, usage of the MEL with the DS caused preventing of these pathological alterations in the kidney. DISCUSSION: We suggested that DS might lead to adverse effects in the kidneys of the rats that are prenatally subjected to this drug. Fortunately, these adverse effects can be prevented by the melatonin supplementation.


Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/toxicity , Antioxidants/pharmacology , Diclofenac/toxicity , Kidney Glomerulus/pathology , Melatonin/pharmacology , Animals , Anti-Inflammatory Agents, Non-Steroidal/pharmacology , Female , Pregnancy , Prenatal Exposure Delayed Effects , Rats , Rats, Wistar
5.
J Obstet Gynaecol Res ; 41(10): 1533-40, 2015 Oct.
Article in English | MEDLINE | ID: mdl-26177586

ABSTRACT

AIM: Pre-eclampsia is a hypertensive disease that is characterized by high blood pressure and proteinuria after 20 gestational weeks and complicates 3-8% of all pregnancies. It is classified as either mild or severe pre-eclampsia according to severity, and the aim of this study was to investigate the structural differences between these two classifications. METHODS: Placenta samples were collected from 68 women who underwent cesarean delivery. Total volume of villi and numerical density of vascular endothelial growth factor (VEGF)- and placental growth factor (PIGF)-positive cells were estimated on stereology and evaluated using one-way ANOVA. RESULTS: There was no significantly difference in total villi volumes between the groups (P > 0.05). In contrast, on immunohistochemistry, the numerical density of VEGF-positive cells in severe pre-eclampsia was significantly different to the control and mild pre-eclampsia groups (P<0.05). Additionally, the numerical density of PIGF-positive cells in the mild and severe pre-eclampsia group was significantly higher than in the control group (P<0.01). CONCLUSION: There is no relationship between villi volume and pre-eclampsia, although growth factors play a role in placental changes. The present results were supported by histopathology and several studies in the literature.


Subject(s)
Placenta Growth Factor/metabolism , Placenta/metabolism , Vascular Endothelial Growth Factor A/metabolism , Adult , Case-Control Studies , Female , Humans , Immunohistochemistry , Placenta/pathology , Pregnancy , Young Adult
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