[1]
|
Sacai, H., Sasaki-Hamada, S., Sugiyama, A., Saitoh, A., Mori, K., Yamada, M. and Oka, J. (2014) The Impairment in Spatial Learning and Hippocampal LTD Induced through the PKA Pathway in Juvenile-Onset Diabetes Rats Are Rescued by Modulating NMDA Receptor Function. Neuroscience Research, 81-82, 55-63.
https://doi.org/10.1016/j.neures.2014.02.002
|
[2]
|
Stevens, M.J., Dananberg, J., Feldman, E.L., Lattimer, S.A., Kamijo, M., Thomas, T.P., Shindo, H., Sima, A.A. and Greene, D.A. (1994) The Linked Roles of Nitric Oxide, Aldose Reductase and (Na+- K+)- ATPase in the Slowing of Nerve Conduction in the Streptozotocin Diabetic Rat. Journal of Clinical Investigation, 94, 853-859.
https://doi.org/10.1172/JCI117406
|
[3]
|
Vague, P., Coste, T.C., Jannot, M.F., Raccah, D. and Tsimaratos, M. (2004) C-Peptide, Na+, K+-ATPase, and Diabetes. Experimental Diabesity Research, 5, 37-50. https://doi.org/10.1080/15438600490424514
|
[4]
|
Welsh, B. and Wecker, L. (1991) Effects of Streptozotocin-Induced Diabetes on Acetylcholine Metabolism in Rat Brain. Neurochemical Research, 16, 453-460. https://doi.org/10.1007/BF00965566
|
[5]
|
Aubier, M. and Viires, N. (1998) Calcium ATPase and Respiratory Muscle Function. The European Respiratory Journal, 11, 758-766.
|
[6]
|
Kamboj, S.S., Chopra, K. and Sandhir, R. (2009) Hyperglycemia-Induced Alterations in Synaptosomal Membrane Fluidity and Activity of Membrane Bound Enzymes: Beneficial Effect of N-Acetylcysteine Supplementation. Neuroscience, 162, 349-358. https://doi.org/10.1016/j.neuroscience.2009.05.002
|
[7]
|
Khakpai, F., Nasehi, M., Haeri-Rohani, A., Eidi, A. and Zarrindast, M.R. (2012) Scopolamine Induced Memory Impairment Possible Involvement of NMDA Receptor Mechanisms of Dorsal Hippocampus and/or Septum. Behavioural Brain Research, 231, 1-10. https://doi.org/10.1016/j.bbr.2012.02.049
|
[8]
|
Szatkowski, M. and Attwell, D. (1994) Triggering and Execution of Neuronal Death in Brain Ischaemia: Two Phases of Glutamate Release by Different Mechanisms. Trends in Neurosciences, 17, 359-365.
https://doi.org/10.1016/0166-2236(94)90040-X
|
[9]
|
Chen, J. and Herrup, K. (2012) Glutamine Acts as a Neuroprotectant against DNA Damage, Beta-Amyloid and H2O2-Induced Stress. PLoS ONE, 7, e33177. https://doi.org/10.1371/journal.pone.0033177
|
[10]
|
Zheng, Y., Yang, Y., Dong, B., Zheng, H., Lin, X., Du, Y., Li, X., Zhao, L. and Gao, H. (2016) Metabonomic Profile Delineate Potential Role of Glutamate-Glutamine Cycle in db/db Mice with Diabetes-Associated Cognitive Decline. Molecular Brain, 18, 9-40. https://doi.org/10.1186/s13041-016-0223-5
|
[11]
|
Pintana, H., Apaijai, N., Pratchayasakul, W., Chattipakorn, N. and Chattipakorn, S.C. (2012) Effects of Metformin on Learning and Memory Behaviors and Brain Mitochondrial Functions in High Fat Diet Induced Insulin Resistant Rats. Life Sciences, 91, 409-414. https://doi.org/10.1016/j.lfs.2012.08.017
|
[12]
|
Yuan, X., Chen, Y.B., Gan, D.N., Cheng, Y.F. and Xu, J.P. (2014) Metformin Improves Learning and Memory of Rats Induced by High-Fat Diet. Military Medical Sciences, 38, 17-21.
|
[13]
|
Zhang, W.H., Liu, Z., Shi, F.G. and Chen, Z.M. (2012). Huanglianwendan Tang in Mice with Type 2 Diabetes and the Impact on the Learning and Memory and the Form of Hippocampal Nerve Cells. Lishizhen Medicine and Materia Medica Research, 23, 948-949.
|
[14]
|
Oliveira, W.H., Nunes, A.K., Franca, M.E., Santos, L.A., Los, D.B., Rocha, S.W., Barbosa, K.P., Rodrigues, G.B. and Peixoto, C.A. (2016) Effect of Metformin on Inflammation and Short-Term Memory in Streptozotocin-Induced Diabetic Mice. Brain Research, 1644, 149-160. https://doi.org/10.1016/j.brainres.2016.05.013
|
[15]
|
Mo, W. and Qian, G.F. (2014) Metformin for High Fat Diet Induced Insulin Resistance the Effect of Space Cognition, Learning and Memory and Cerebral Energy Metabolism. Chinese Journal of Gerontology, 34, 2813-2815.
|
[16]
|
Asadbegi, M., Yaghmaei, P., Salehi, I., Ebrahim-Habibi, A. and Komaki, A. (2016) Neuroprotective Effects of Metformin against a β-Mediated Inhibition of Long-Term Potentiation in Rats Fed a High-Fat Diaet. Brain Research Bulletin, 121, 178-185. https://doi.org/10.1016/j.brainresbull.2016.02.005
|
[17]
|
Anwar, M. and Meki, A. (2003) Oxidative Stress in Streptozotocin-Induced Diabetic Rats: Effects of Garlic Oil and Melatonin. Comparative Biochemistry and Physiology Part A, 135, 539-547.
https://doi.org/10.1016/S1095-6433(03)00114-4
|
[18]
|
Thomson, M., Al-Amin, Z.M., Al-Qattan, K.K., Shaban, L.H. and Ali, M. (2006) Anti-Diabetic and Hypolipidaemic Properties of Garlic (Allium sativum) in Streptozotocin Induced Diabetic Rats. International Journal of Diabetes and Metabolism, 15, 108-115.
|
[19]
|
Drobiova, H., Thomson, M., Al-Qattan, K., Peltonen-Shalaby, R., Al-Amin, Z. and Ali, M. (2011) Garlic Increases Antioxidant Levels in Diabetic and Hypertensive Rats Determined by a Modified Peroxidase Method. Evidence-Based Complementary and Alternative Medicine, 2011, Article ID: 703049.
|
[20]
|
Liu, C.T., Hse, H., Lii, C.K., Chen, P.S. and Sheen, L.Y. (2005) Effects of Garlic Oil and Diallyl Trisulfide on Glycemic Control in Diabetic Rats. European Journal of Pharmacology, 516, 165-173.
https://doi.org/10.1016/j.ejphar.2005.04.031
|
[21]
|
Shiju, T.M., Rajesh, N.G. and Viswanathan, P. (2013) Renoprotective Effect of Aged Garlic Extract in Streptozotocin-Induced Diabetic Rats. Indian Journal of Pharmacology, 45, 18-23.
|
[22]
|
Sarkaki, A., Valipour, S.C., Farbood, Y., Mohammad, S., Mansouri, T., Naghizadeh, B. and Basirian, E. (2013) Effects of Fresh, Aged and Cooked Garlic Extracts on Short- and Long-Term Memory in Diabetic Rats. Avicenna Journal of Phytomedicine, 3, 45-55.
|
[23]
|
Safiriyu, A.A., Semuyaba, I., RemónFigueredo, N., Etibor, T.A. and Ajibola, M.I. (2017) Garlic Extract (Allium sativum) Enhances Spatial Working Memory in Wistar Rats: Involvement of Hippocampal Na+/K+ ATPase and Ca2+ ATPase Activities. Journal of Behavioral and Brain Science, 7, 31-40.
https://doi.org/10.4236/jbbs.2017.72004
|
[24]
|
Semuyaba, I., Safiriyu, A.A., Tiyo, E.A. and Remón-Figueredo, N. (2017) Memory Improvement Effect of Ethanol Garlic (A. sativum) Extract in Streptozotocin-Nicotinamide Induced Diabetic Wistar Rats Is Mediated through Increasing of Hippocampal Sodium-Potassium ATPase, Glutamine Synthetase, and Calcium ATPase Activities. Evidence-Based Complementary and Alternative Medicine, 3, 1-7.
https://doi.org/10.1155/2017/3720380
|
[25]
|
Homayounfar, H., BaluchnejadMojarad, T., Roghani, M., Hosseini, M. and Kamalinejad, M. (2003) Effect of Aqueous Garlic (Allium sativum L.) Extract on Acetylcholine and Isosorbide-Induced Relaxation of Isolated Aorta in Rat. Iranian Biomedical Journal, 7, 23-27.
|
[26]
|
Marudamuthu, A.S. and Leelavinothan, P. (2008) Emerging Targets Effect of Pterostilbene on Lipids and Lipid Profiles in Streptozotocin-Nicotinamide Induced Type 2. Journal of Applied Biomedicine, 6, 31-37.
|
[27]
|
Tirri, R., Lagrspetz, K.Y.H. and Kohomen, J. (1973) Temperature Dependence of the ATPase Activity in Brain Homogenates during the Postnatal Development of Rat. Comparative Biochemistry and Physiology, 44, 473-480.
|
[28]
|
Fiske, C.H. and Subba Row, Y. (1925) The Colorimetric Determination of Phosphates. The Journal of Biological Chemistry, 66, 375-400.
|
[29]
|
Desaiah, D. and Ho, I.K. (1979) Effect of Acute and Continuous Morphine Administration on Catecholamine-Sensitive Adenosine Triphosphatase in Mouse Brain. Journal of Pharmacology and Experimental Therapeutics, 208, 80-85.
|
[30]
|
Rowe, W.B., Ronzio, R.A., Wellner, V.P. and Meister, A. (1970) Glutamine Synthetase (Sheep Brain) Methods. Enzymology, 17, 900-910. https://doi.org/10.1016/0076-6879(71)17304-1
|
[31]
|
Lotfi, N., Hami, J., Hosseini, M., Haghir, D. and Haghir, H. (2016) Diabetes during Pregnancy Enhanced Neuronal Death in the Hippocampus of Rat Offspring. International Journal of Developmental Neuroscience, 51, 28-35. https://doi.org/10.1016/j.ijdevneu.2016.04.009
|
[32]
|
Sadeghi, A., Ebrahimzadeh Bideskan, A.R., Alipour, F., Fazel, A.R. and Haghir, A. (2013) The Effect of Ascorbic Acid and Garlic Administration on Lead-Induced Neural Damage in Rat Offspring’s Hippocampus. Iranian Journal of Basic Medical Sciences, 16, 157-164.
|
[33]
|
Wang, J., Gallagher, D., DeVito, L.M., Cancino, G.I., Tsui, D., He, L., Keller, G.M., Frankland, P.W., Kaplan, D.R. and Miller, F.D. (2012) Metformin Activates an Atypical PKC-CBP Pathway to Promote Neurogenesis and Enhance Spatial Memory Formation. Cell Stem Cell, 11, 23-35. https://doi.org/10.1016/j.stem.2012.03.016
|
[34]
|
Lennox, R., Porter, D.W., Flatt, P.R., Holscher, C., Irwin, N. and Gault, V.A. (2014) Comparison of the Independent and Combined Effects of Sub-Chronic Therapy with Metformin and a Stable GLP-1 Receptor Agonist on Cognitive Function, Hippocampal Synaptic Plasticity and Metabolic Control in High-Fat Fed Mice. Neuropharmacology, 86, 22-30. https://doi.org/10.1016/j.neuropharm.2014.06.026
|