LIVIVO - The Search Portal for Life Sciences

zur deutschen Oberfläche wechseln
Advanced search

Search results

Result 1 - 3 of total 3

Search options

  1. Article ; Online: Proxeed plus salvage rat testis from ischemia- reperfused injury by enhancing antioxidant's activities and inhibition of iNOS expression.

    Sangodele, Janet Olayemi / Inuwa, Zephaniah / Lawal, Bashir / Adebayo-Gege, Grace / Okoli, Bamidele Joseph / Mtunzi, Fanyana

    Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie

    2020  Volume 133, Page(s) 111086

    Abstract: Testicular torsion is an acute urological emergency condition that occurs due to obstruction of blood flow to the testicles which may result in ischemia and loss of testicular functions. This study examined the protective effects of Proxeed Plus (PP), a ... ...

    Abstract Testicular torsion is an acute urological emergency condition that occurs due to obstruction of blood flow to the testicles which may result in ischemia and loss of testicular functions. This study examined the protective effects of Proxeed Plus (PP), a dietary supplement on testicular ischemia/reperfusion (I/R) injured rats using oxidative stress markers, hormonal levels, apoptotic parameters, histological and immunohistochemistry analysis at 4 h and after 7 days of reperfusion. The protective treatment of the I/R injured rats with PP at 1000 and 5000 mg/kg body weight (bw) resulted in significant increases in the serum and tissue antioxidative defense capacities (superoxide dismutase, reduced glutathione, catalase, glutathione-s-transferase, and glutathione peroxidase), sex hormones (luteinizing hormone, follicle-stimulating hormone, and testosterone), also reduce pro-oxidative markers (malondialdehyde and hydrogen peroxide), serum iNOS and apoptotic parameters (Caspase -3 and Caspase -9) in comparison to the results detected in the I/R untreated rats. It was also observed that PP ameliorated histological changes of I/R injured rats; increased spermatogenetic activity, seminiferous tubular diameter, Leydig cell mass, and reduced expressions of testicular inducible nitric oxide synthase (iNOS). Therefore, the therapeutic use of Proxeed Plus could be considered a promising approach in averting testicular damage against I/R injury.
    MeSH term(s) Animals ; Antioxidants/pharmacology ; Apoptosis/drug effects ; Biomarkers/blood ; Dietary Supplements ; Disease Models, Animal ; Enzyme Inhibitors/pharmacology ; Male ; Nitric Oxide Synthase Type II/antagonists & inhibitors ; Nitric Oxide Synthase Type II/metabolism ; Oxidative Stress/drug effects ; Rats ; Rats, Wistar ; Reperfusion Injury/enzymology ; Reperfusion Injury/pathology ; Reperfusion Injury/prevention & control ; Signal Transduction ; Spermatic Cord Torsion/drug therapy ; Spermatic Cord Torsion/enzymology ; Spermatic Cord Torsion/pathology ; Spermatogenesis/drug effects ; Testis/drug effects ; Testis/enzymology ; Testis/pathology
    Chemical Substances Antioxidants ; Biomarkers ; Enzyme Inhibitors ; Nitric Oxide Synthase Type II (EC 1.14.13.39) ; Nos2 protein, rat (EC 1.14.13.39)
    Language English
    Publishing date 2020-12-11
    Publishing country France
    Document type Journal Article
    ZDB-ID 392415-4
    ISSN 1950-6007 ; 0753-3322 ; 0300-0893
    ISSN (online) 1950-6007
    ISSN 0753-3322 ; 0300-0893
    DOI 10.1016/j.biopha.2020.111086
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  2. Article: The para isomer of dinitrobenzene disrupts redox homeostasis in liver and kidney of male wistar rats.

    Sangodele, Janet Olayemi / Olaleye, Mary Tolulope / Monsees, Thomas K / Akinmoladun, Afolabi Clement

    Biochemistry and biophysics reports

    2017  Volume 10, Page(s) 297–302

    Abstract: Background: Para: Methods: Forty eight male Wistar rats weighing 160-180 g were administered 50, 75, 1000 and 2000 mg/kg b.wt (body weight) of : Results: Compared with control animals, : Conclusions: Our findings show that sub-chronic oral and ... ...

    Abstract Background: Para
    Methods: Forty eight male Wistar rats weighing 160-180 g were administered 50, 75, 1000 and 2000 mg/kg b.wt (body weight) of
    Results: Compared with control animals,
    Conclusions: Our findings show that sub-chronic oral and sub-dermal administration of
    Language English
    Publishing date 2017-05-04
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 2831046-9
    ISSN 2405-5808
    ISSN 2405-5808
    DOI 10.1016/j.bbrep.2017.04.017
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  3. Article ; Online: The para isomer of dinitrobenzene disrupts redox homeostasis in liver and kidney of male wistar rats

    Janet Olayemi Sangodele / Mary Tolulope Olaleye / Thomas K. Monsees / Afolabi Clement Akinmoladun

    Biochemistry and Biophysics Reports, Vol 10, Iss C, Pp 297-

    2017  Volume 302

    Abstract: Background: Para-Dinitrobenzene (p-DNB) is one of the isomers of dinitrobenzene which have been detected as environmental toxicants. Skin irritation and organ toxicities are likely for industrial workers exposed to p-DNB. This study evaluated the effect ... ...

    Abstract Background: Para-Dinitrobenzene (p-DNB) is one of the isomers of dinitrobenzene which have been detected as environmental toxicants. Skin irritation and organ toxicities are likely for industrial workers exposed to p-DNB. This study evaluated the effect of sub-chronic exposure of rats to p-DNB on cellular redox balance, hepatic and renal integrity. Methods: Forty eight male Wistar rats weighing 160–180 g were administered 50, 75, 1000 and 2000 mg/kg b.wt (body weight) of p-DNB or an equivalent volume of vehicle (control) orally and topically for 14 days. After the period of treatment, the activities of kidney and liver catalase (CAT), alkaline phosphatase (ALP) and superoxide dismutase (SOD) as well as extent of renal and hepatic lipid peroxidation (LPO) were determined. Serum ALP activity and plasma urea concentration were also evaluated. Results: Compared with control animals, p-DNB -administered rats showed decrease in the body and relative kidney and liver weights as well as increased renal and hepatic hydrogen peroxide and lipid peroxidation levels accompanied by decreased superoxide dismutase and catalase activities. However, p-DNB caused a significant increase in plasma urea concentration and serum, liver and kidney ALP activities relative to control. In addition, p-DNB caused periportal infiltration, severe macro vesicular steatosis and hepatic necrosis in the liver. Conclusions: Our findings show that sub-chronic oral and sub-dermal administration of p-DNB may produce hepato-nephrotoxicity through oxidative stress.
    Keywords Environmental toxicants ; Kidney ; Liver ; p‐DNB ; Oxidative stress ; Sub-dermal ; Biology (General) ; QH301-705.5 ; Biochemistry ; QD415-436
    Subject code 630
    Language English
    Publishing date 2017-07-01T00:00:00Z
    Publisher Elsevier
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

To top