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Dr
Osunsanmi, Foluso Oluwagbemiga
Department: Agriculture
Research Interest(s): Clinical biochemistry, Bio-informatics, Food biochemistry, Plants biochemistry, Medicinal chemistry, Ethno-pharmacology, Natural product synthetic chemistry, Functional food, Metabolic diseases, Nutritional biochemistry, Microbiology, Biotechnology, Proteomics.
Biography: Dr. Foluso O Osunsanmi is currently a Research Fellow at the Department of Biochemistry and Microbiology, University of Zululand, South Africa. He is a biochemist with twenty years’ work experiences both in academic and industrial sectors. He had supervised both undergraduate and postgraduate students. He also has notable numbers of publications in reputable journals and had presented both in local and international conferences. He regularly performs peer reviews for over twenty-two different reputable journals. He is an Academic Editor of many International journals. He is also member of South Africa Association Council for Natural Scientific Professions, South Africa Association of Clinical Biochemistry, South Africa Association of Botanist and National Association of Safety professional.
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- Considering the global health threat posed by kidney disease burden, a search for new nephroprotective drugs from our local flora could prove a powerful strategy to respond to this health threat. In this study we investigated the antihyperuricemic and nephroprotective potential of RA-3, a plant-derived lanosteryl triterpene. The antihyperuricemic and nephroprotective effect of RA-3 was investigated using the adenine and gentamicin induced hyperuricemic and nephrotoxicity rat model. Following the induction of hyperuricemia and nephrotoxicity, the experimental model rats (Sprague Dawley) were orally administered with RA-3 at 50 and 100 mg/kg body weight, respectively, daily for 14 days. Treatment of the experimental rats with RA-3, especially at 100 mg/kg, effectively lowered the serum renal dysfunction (blood urea nitrogen and creatinine) and hyperuricemic (uric acid and xanthine oxidase) biomarkers. These were accompanied by increased antioxidant status with decrease in malondialdehyde content. A much improved histomorphological structure of the kidney tissues was also observed in the triterpene treated groups when compared to the model control group. It is evident that RA-3 possesses the antihyperuricemic and nephroprotective properties, which could be vital for prevention and amelioration of kidney disease.
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- Inula glomerata Oliv. & Hiern and Salacia kraussii (Harv.) Harv are medicinal plants used by traditional healers in remote areas of Mbazwana, Northern KwaZulu-Natal, South Africa for ameliorating male sexual disorders including erectile dysfunction (ED), low sperm count and early ejaculation. The study aimed at determining the ameliorative effect of the methanolic crude extracts of Inula glomerata (I. glomerata) and Salacia kraussii (S. kraussii) on butanol-induced erectile dysfunction in Sprague Dawley rats. The crude extract was prepared by maceration using methanol. Animal study was conducted whereby thirty-five male Sprague Dawley rats were divided into seven experimental groups: normal group, n-but (10 mg/kg), n-but+ Ig (50 and 250 mg/kg), n-but+ Sk (50 and 250 mg/kg) and n-but+ Cialis (5mg/kg). The experiment lasted for 28 days, after which various biochemical assays (acetylcholinesterase, ACE, arginase, testosterone, and uric acid) was done. The cytotoxicity of the crude extracts was also determined. The results revealed that n-butanol induced erectile dysfunction in the rats by decreasing mounting frequency, testosterone and nitric oxide level and simultaneously elevated the activities of arginase and acetylcholinesterase. The plants however, inhibited arginase and acetylcholinesterase when compared to the untreated. Furthermore, the plants’ extracts were able to increase the level of testosterone and nitric oxide. It can be inferred that both plants could be promising natural therapy for erectile dysfunction. Nonetheless, the plants’ extracts are toxic hence should be taken with caution.
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- Diabetes mellitus remains a global health issue despite the advance in orthodox medicine. This study investigated the in vitro antioxidant and antidiabetic potential of crude extracts from the seed coat and pulp of Strychnos madagascariensis. The phytochemical screening was carried out using standard protocols. Different extracts were prepared from the fruit parts by maceration using methanol, n-hexane, ethyl acetate, and water for antioxidant and antidiabetic assays, and their percentage yield was calculated. The antioxidant potential of the extracts was determined using 2,2’-azino-bis (3-ethylbenzothiazoline-6-sulphonic acid (ABTS) and 2’2- diphenyl-1-picrylhydrazyl (DPPH). Antidiabetic activities of the extracts were investigated using α-amylase, α-glucosidase, and pancreatic lipase assays. Terpenoids, alkaloids and cardiac glycosides were present in both the fruit parts. However, saponin present in the fruit pulp was absent in the seed coat (testa). The percentage yields are as follows; water > ethyl acetate > hexane > methanol (seed coat) and methanol > water > ethyl acetate > hexane (fruit pulp), respectively. The crude extracts scavenged ABTS and DPPH radicals in different degrees. The aqueous extract of the pulp and seed coat (testa) showed significant (P < 0.05) higher scavenging activity against ABTS (IC50; 0.012 and 0.006 mg/ml) and DPPH (IC50; 0.06 mg/ml and 0.064 mg/ml) radicals than other extracts. The crude extracts inhibited α-amylase, α-glucosidase, and pancreatic lipase. The aqueous and methanol extracts of the fruit parts showed better amylase inhibitory activity than other extracts. The aqueous extract of the seed coat (IC50; 0.0785 mg/ml) showed the highest glucosidase inhibitory activity. In addition, methanol extract of the seed coat (IC50; 0.069 mg/ml) exhibited the highest inhibitory activity on pancreatic lipase compared to the extracts in other solvents. Hence, the aqueous and methanol crude extracts of Strychnos madagascariensis seed coat and fruit pulp could be used in the preparation of nutraceutical products for managing diabetic mellitus.
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- The treatment of diseases is under threat due to the increasing resistance of disease-causing bacteria to antibiotics. Likewise, free radical-induced oxidative stress has been implicated in several human disease conditions, such as cancer, stroke and diabetes. In the search for amino acid analogues with antibacterial and antioxidant properties as possible mimics of antimicrobial peptides, substituted N-(2′-nitrophenyl)pyrrolidine-2-carboxamides 4a–4k and N-(2′-nitrophenyl)piperidine-2-carboxamides 4l–4n have been synthesized via a two-step, one-pot amidation of the corresponding acids, using thionyl chloride with different amines in dichloromethane. The carboxamides were characterized by infrared and nuclear magnetic resonance spectroscopy, mass spectrometry and elemental analysis. Carboxamides 4a–4n were assayed against five Gram-positive and five Gram-negative bacterial strains using the broth micro-dilution procedure and compared to standard antibiotic drugs (streptomycin and nalidixic acid). 4b showed the highest antibacterial activity with a minimum inhibitory concentration (MIC) value of 15.6 µg/mL against Staphylococcus aureus. Pertinently, 4b and 4k are promising candidates for narrow-spectrum (Gram-positive) and broad-spectrum antibiotics, respectively. The antioxidant properties of the carboxamides were also evaluated using the 1,1-diphenyl-2-picryl hydrazyl (DPPH) radical and 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid) (ABTS) radical cation. 4a and 4k recorded the lowest IC50 values of 1.22 × 10–3 mg/mL (with DPPH) and 1.45 × 10–4 mg/mL (with ABTS), respectively. Notably, 4k recorded about 2.5 times better antioxidant capacity than the positive controls – ascorbic acid and butylated hydroxyanisole. These results bode well for N-aryl carboxamides as good mimics and substitutes for antimicrobial peptides towards mitigating bacterial resistance to antibiotics as well as ameliorating oxidative stress-related diseases.
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- This study investigated anti-viral, antioxidant activity and anti-pyretic of crude extract from Artemisia afra, Artemisia absinthium and Pittiosporum viridflorum leaves. The crude extracts were prepared by maceration using aqueous, methanol and dichloromethane respectively. Antiviral studies were evaluated with influenza virus using Fluorescence based - Neuraminidase inhibitors. Antioxidant activities determined with DPPH, Nitric oxide, hydroxyl and super oxide anion radicals’ Anti-pyretic activities were evaluated using rats with yeast induced pyrexia. Total phenol, flavonoids, and proanthocyanin contents of the plants samples were evaluated using standard protocols. The crude extracts exhibited neuraminidase inhibitory activity against the influenza virus at different thresholds. Artemisia absinthium aqueous extract showed the best activity against A/Sydney/5/97. Whereas Artemisia afra methanol crude extract displayed highest antioxidant potential against the tested antioxidant parameters. All the crude extracts significantly reversed yeast induced pyrexia in rats, similar to paracetamol. Thus, they could serve as natural remedy for respiratory diseases such as Influenza.
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- Reports from previous studies now provide evidence that dyslipidaemia and oxidative stress play crucial roles in the pathogenesis and progression of diabetes and its related complications. This research is aimed to investigate the potential effects of protein isolate from Parkia biglobosa seeds (PBPI) in streptozotocin (STZ)-induced diabetic rats by measuring blood glucose levels, changes in lipid metabolism and biomarkers of oxidative stress. Diabetic rats were treated orally with graded doses of PBPI, 200 mg/kg bw and 400 mg/kg bw, and 5 U/kg, intraperitoneal (i.p.) of insulin once daily for 28 days with the fasting blood glucose (FBG) monitored weekly. The effect of PBPI on the serum lipid profile was measured while the extent of lipid peroxidation (LPO), as well as antioxidant parameters (superoxide dismutase; SOD, catalase; CAT, glutathione-S-transferase; GST and total glutathione; total GSH), was determined in the cardiac homogenates of diabetic rats. At the tested doses, treatment with PBPI was significantly effective in lowering FBG, serum triglyceride, cholesterol, low-density lipoprotein cholesterol (LDL-c) and very low-density lipoprotein cholesterol (VLDL-c), while concurrently increasing high-density lipoprotein cholesterol (HDL-c). PBPI also significantly decreased the elevations witnessed in LPO levels and restored the biomarkers of oxidative stress in the cardiac homogenate of experimental rats. The results from this study demonstrate that PBPI could improve dyslipidaemia and cardiac oxidative stress in the experimental diabetic animal model possibly by reducing and effectively scavenging reactive oxygen species (ROS) production as well as by increasing antioxidant capacity in combating oxidative stress. Therefore, it can be concluded that PBPI could be explored in the development of a potent cardioprotective supplement or adjuvant therapy towards the management of diabetes and its related complications.
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