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Nose to brain drug delivery - A promising strategy for active components from herbal medicine for treating cerebral ischemia reperfusion
Abstract
Cerebral ischemia reperfusion injury (CIRI), one of the major causes of death from stroke in the world, not only causes tremendous damage to human health, but also brings heavy economic burden to society. Current available treatments for CIRI, including mechanical therapies and drug therapies, are often accompanied by significant side-effects. Therefore, it is necessary to discovery new strategies for treating CIRI. Many studies have confirmed that the herbal medicine has the advantages of abundant resources, good curative effect and little side effects, which can be used as potential drug for treatment of CIRI through multiple targets. It's known that oral administration commonly has low bioavailability, and injection administration is inconvenient and unsafe. Many drugs can't delivery to brain through routine pathways due to the blood-brain-barrier (BBB). Interestingly, increasing evidences have suggested the nasal administration is a potential direct route to transport drug into brain avoiding the BBB and has the characteristics of high bioavailability for treating brain diseases. Therefore, intranasal administration can be treated as an alternative way to treat brain diseases. In the present review, effective methods to treat CIRI by using active ingredients derived from herbal medicine through nose to brain drug delivery (NBDD) are updated and discussed, and some related pharmacological mechanisms have also been emphasized. Our present study would be beneficial for the f…
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“EVs, which are characterized by low immunogenicity, good natural stability, long half-life, high delivery rate, and the ability to cross the BBB, have become a research hotspot for safe and effective brain drug delivery carriers [31, 32].”
From Engineered Extracellular Vesicles Loaded with MiR-100-5p Antagonist Selectively Target the Lesioned Region to Promote Recovery from Brain Damage (2025) · cites this paper as [31]
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Mechanism of intranasal drug delivery directly to the brain
Crowe, T. P., Greenlee, M. H. W., Kanthasamy, A. G., & Hsu, W. H. (2018) · Life Sciences · doi:10.1016/j.lfs.2017.12.025 · Cited by 721
Intranasal Drug Delivery: How, Why and What For?
Pires, A., Fortuna, A., Alves, G., & Falcão, A. (2009) · Journal of Pharmacy & Pharmaceutical Sciences · doi:10.18433/j3nc79 · Cited by 641
Pardeshi, C. V., & Belgamwar, V. S. (2013) · Expert Opinion on Drug Delivery · doi:10.1517/17425247.2013.790887 · Cited by 482
Gänger, S., & Schindowski, K. (2018) · Pharmaceutics · doi:10.3390/pharmaceutics10030116 · Cited by 447
Progress in brain targeting drug delivery system by nasal route
Khan, A. R., Liu, M., Khan, M. W., & Zhai, G. (2017) · Journal of Controlled Release · doi:10.1016/j.jconrel.2017.09.001 · Cited by 402
Insights into Direct Nose to Brain Delivery: Current Status and Future Perspective
Mittal, D., Ali, A., Md, S., Baboota, S., Sahni, J. K., & Ali, J. (2014) · Drug Delivery · doi:10.3109/10717544.2013.838713 · Cited by 359
Recent advances in carrier mediated nose-to-brain delivery of pharmaceutics
Bourganis, V., Kammona, O., Alexopoulos, A., & Kiparissides, C. (2018) · European Journal of Pharmaceutics and Biopharmaceutics · doi:10.1016/j.ejpb.2018.05.009 · Cited by 357
The nasal delivery of nanoencapsulated statins – an approach for brain delivery
Clementino, A., Batger, M., Garrastazu, G., Pozzoli, M., Del Favero, E., Rondelli, V., Gutfilen, B., Barboza, T., Sukkar, M. B., Souza, S. A. L., et al. (2016) · International Journal of Nanomedicine · doi:10.2147/ijn.s119033 · Cited by 81
Research works printed but not linked: 211
- GBD, 2017, Lancet, 390, 1260, 10.1016/S0140-6736(17)32130-X · DOI · Paper page
- Randolph, 2016, Ischemic stroke, Workplace Health Saf., 64, 444, 10.1177/2165079916665400 · DOI
- Ou, 2017, MiR-375 attenuates injury of cerebral ischemia/reperfusion via targeting Ctgf, Biosci. Rep., 37, 10.1042/BSR20171242 · DOI
- Zhang, 2016, Protective effects of mangiferin on cerebral ischemia-reperfusion injury and its mechanisms, Eur. J. Pharmacol., 771, 145, 10.1016/j.ejphar.2015.12.003 · DOI · Paper page
- Taoufik, 2008, Ischemic neuronal damage, Curr. Pharm. Des., 14, 3565, 10.2174/138161208786848748 · DOI
- Guo, 2019, Natural compound methyl protodioscin protects rat brain from ischemia/reperfusion injury through regulation of Mul1/SOD2 pathway, Eur. J. Pharmacol., 849, 50, 10.1016/j.ejphar.2019.01.057 · DOI
- Doyle, 2008, Mechanisms of ischemic brain damage, Neuropharmacology, 55, 310, 10.1016/j.neuropharm.2008.01.005 · DOI
- Hentia, 2018, An overview of protective strategies against ischemia/reperfusion injury: the role of hyperbaric oxygen preconditioning, Brain Behav., 8, 10.1002/brb3.959 · DOI
- Wang, 2019, Electroacupuncture ameliorates neuronal injury by Pink1/Parkin-mediated mitophagy clearance in cerebral ischemia-reperfusion, Nitric Oxide, 91, 23, 10.1016/j.niox.2019.07.004 · DOI
- Tsivgoulis, 2018, Successful reperfusion with intravenous thrombolysis preceding mechanical thrombectomy in large-vessel occlusions, Stroke, 49, 232, 10.1161/STROKEAHA.117.019261 · DOI
- Zhao, 2011, Postischemic administration of liposome-encapsulated luteolin prevents against ischemia-reperfusion injury in a rat middle cerebral artery occlusion model, J. Nutr. Biochem., 22, 929, 10.1016/j.jnutbio.2010.07.014 · DOI
- Savitz, 2017, Reconsidering neuroprotection in the reperfusion era, Stroke, 48, 3413, 10.1161/STROKEAHA.117.017283 · DOI
- Liu, 2017, Effect of ulinastatin on the permeability of the blood-brain barrier on rats with global cerebral ischemia/reperfusion injury as assessed by MRI, Biomed. Pharmacother., 85, 412, 10.1016/j.biopha.2016.11.044 · DOI
- Li, 2017, Ulinastatin downregulates TLR4 and NF-kB expression and protects mouse brains against ischemia/reperfusion injury, Neurol. Res., 39, 367, 10.1080/01616412.2017.1286541 · DOI
- Kwon, 2015, Nafamostat mesilate attenuates transient focal ischemia/reperfusion-induced brain injury via the inhibition of endoplasmic reticulum stress, Brain Res., 1627, 12, 10.1016/j.brainres.2015.09.013 · DOI
- Chen, 2014, Nafamostat mesilate attenuates neuronal damage in a rat model of transient focal cerebral ischemia through thrombin inhibition, Sci. Rep., 4, 5531, 10.1038/srep05531 · DOI
- Izuma, 2018, Thrombolysis with rt-PA under rivaroxaban anticoagulation in a hypertensive rat model of intraluminal middle cerebral artery occlusion, J. Stroke Cerebrovasc. Dis., 27, 2761, 10.1016/j.jstrokecerebrovasdis.2018.06.003 · DOI
- Morihara, 2017, Reduction of intracerebral hemorrhage by rivaroxaban after tPA thrombolysis is associated with downregulation of PAR‐1 and PAR‐2, J. Neurosci. Res., 95, 1818, 10.1002/jnr.24013 · DOI
- Zheng, 2006, Inhibitory action of propyl gallate on the activation of SAPK/JNK and p38MAPK induced by cerebral ischemia-reperfusion in rats, Acta Pharm. Sin. B, 41, 548
- Berekashvili, 2018, Safety and feasibility of argatroban, recombinant tissue plasminogen activator, and intra-arterial therapy in stroke (ARTSS-IA Study), J. Stroke Cerebrovasc. Dis., 27, 3647, 10.1016/j.jstrokecerebrovasdis.2018.08.036 · DOI
- Xue, 2017, Calcium-sensing receptor antagonist NPS2390 attenuates neuronal apoptosis though intrinsic pathway following traumatic brain injury in rats, Biochem. Biophys. Res. Commun., 486, 589, 10.1016/j.bbrc.2017.03.097 · DOI
- Wada, 2014, Effects of edaravone on early outcomes in acute ischemic stroke patients treated with recombinant tissue plasminogen activator, J. Neurol. Sci., 345, 106, 10.1016/j.jns.2014.07.018 · DOI
- Huang, 2017, S-oxiracetam protect against ischemic stroke via alleviating blood brain barrier dysfunction in rats, Eur. J. Pharm. Sci., 109, 40, 10.1016/j.ejps.2017.07.029 · DOI
- Llorente, 2013, Unfolded protein response to global ischemia following 48 h of reperfusion in the rat brain: the effect of age and meloxicam, J. Neurochem., 127, 701, 10.1111/jnc.12337 · DOI
- Lu, 2014, Distribution of α-asarone in brain following three different routes of administration in rats, Eur. J. Pharm. Sci., 63, 63, 10.1016/j.ejps.2014.06.006 · DOI
- Dobrivojević, 2015, Involvement of bradykinin in brain edema development after ischemic stroke, Pflugers Arch., 467, 201, 10.1007/s00424-014-1519-x · DOI
- Li, 2016, Multi-target strategy and experimental studies of traditional Chinese medicine for alzheimer’s disease therapy, Curr. Top. Med. Chem., 16, 537, 10.2174/1568026615666150813144003 · DOI
- Zhang, 2019, Guizhi-Shaoyao-Zhimu decoction possesses anti-arthritic effects on type II collagen-induced arthritis in rats via suppression of inflammatory reactions, inhibition of invasion & migration and induction of apoptosis in synovial fibroblasts, Biomed. Pharmacother., 118, 10.1016/j.biopha.2019.109367 · DOI
- Sun, 2015, Ameliorating effects of traditional Chinese medicine preparation, Chinese materia medica and active compounds on ischemia/reperfusion-induced cerebral microcirculatory disturbances and neuron damage, Acta Pharm. Sin. B, 5, 8, 10.1016/j.apsb.2014.11.002 · DOI
- Gao, 2015, Ligustrazine monomer against cerebral ischemia/reperfusion injury, Neural Regen. Res., 10, 832, 10.4103/1673-5374.156991 · DOI
- Miyake, 2015, The blood-brain barrier and nasal drug delivery to the central nervous system, Am. J. Rhinol. Allergy, 29, 124, 10.2500/ajra.2015.29.4149 · DOI · Paper page
- Kapoor, 2016, A review of intranasal formulations for the treatment of seizure emergencies, J. Control Release., 237, 147, 10.1016/j.jconrel.2016.07.001 · DOI
- Vyas, 2005, Intranasal drug delivery for brain targeting, Curr. Drug Deliv., 2, 165, 10.2174/1567201053586047 · DOI
- Battaglia, 2018, Lipid nanoparticles for intranasal administration: application to nose-to-brain delivery, Expert Opin. Drug Deliv., 15, 369, 10.1080/17425247.2018.1429401 · DOI
- Lochhead, 2012, Intranasal delivery of biologics to the central nervous system, Adv. Drug Deliv. Rev., 64, 614, 10.1016/j.addr.2011.11.002 · DOI · Paper page
- Johanson, 2016, Merging transport data for choroid plexus with blood-brain barrier to model CNS homeostasis and disease more effectively, CNS Neurol. Disord. Drug Targets, 15, 1151, 10.2174/1871527315666160915120758 · DOI
- Grassin-Delyle, 2012, Intranasal drug delivery: an efficient and non-invasive route for systemic administration: focus on opioids, Pharmacol. Ther., 134, 366, 10.1016/j.pharmthera.2012.03.003 · DOI · Paper page
- Selvaraj, 2018, Nose to brain transport pathways an overview: potential of nanostructured lipid carriers in nose to brain targeting, Artif. Cells Nanomed. Biotechnol., 46, 2088
- John, 2014, Burkholderia pseudomallei penetrates the brain via destruction of the olfactory and trigeminal nerves: implications for the pathogenesis of neurological melioidosis, MBio, 5
- Ma, 2008, Trigeminal nerve pathway to brain following intranasal administration of transforming growth factor beta 1, Med. J. Chin. PLA., 33, 219
- John, 2016, Burkholderia pseudomallei rapidly infects the brain stem and spinal cord via the trigeminal nerve after intranasal inoculation, Infect. Immun., 84, 2681, 10.1128/IAI.00361-16 · DOI
- Hanson, 2007, Strategies for intranasal delivery of therapeutics for the prevention and treatment of neuroAIDS, J. Neuroimmune Pharmacol., 2, 81, 10.1007/s11481-006-9039-x · DOI
- Miyamoto, 2001, Effect of poly-L-arginine on the nasal absorption of FTIR-dextran of different molecular weights and recombinant human granulocyte colony stimulating factor (RHG-SF) in rats, Int. J. Pharm., 226, 127, 10.1016/S0378-5173(01)00797-9 · DOI
- Brightman, 1976, The morphological approach to the study of normal and abnormal brain permeability, Adv. Exp. Med. Biol., 69, 41, 10.1007/978-1-4684-3264-0_4 · DOI
- Chatterjee, 2017, Nose to brain drug delivery: a recent update, J. Formul. Sci. Bioavailab., 1
- Wu, 2008, From nose to brain: understanding transport capacity and transport rate of drugs, Expert Opin. Drug Deliv., 5, 1159, 10.1517/17425247.5.10.1159 · DOI
- Garg, 2015, Current nanotechnological approaches for an effective delivery of bioactive drug molecules to overcome drug resistance tuberculosis, Curr. Pharm. Des., 21, 3076, 10.2174/1381612821666150531163254 · DOI
- Dai, 2018, Neuroprotective effect of baicalin on focal cerebral ischemia in rats, Neural Regen. Res., 13, 2129, 10.4103/1673-5374.241464 · DOI
- Zhou, 2014, Baicalin attenuates brain edema in a rat model of intracerebral hemorrhage, Inflammation, 37, 107, 10.1007/s10753-013-9717-9 · DOI
- Xue, 2010, Baicalin attenuates focal cerebral ischemic reperfusion injury through inhibition of nuclear factor κB p65 activation, Biochem. Biophys. Res. Commun., 403, 398, 10.1016/j.bbrc.2010.11.042 · DOI
- Li, 2011, Evaluation of brain-targeting of nasal baicalin-phospholipid complex in situ gel, Chin. Pharm. J., 46, 1254
- Li, 2018, Preparation, characterization, pharmacokinetics and biodistribution of baicalin-loaded liposome on cerebral ischemia-reperfusion after iv administration in rats, Molecules, 23, 1747, 10.3390/molecules23071747 · DOI
- Xiang, 2020, Pharmacokinetics, pharmacodynamics and toxicity of Baicalin liposome on cerebral ischemia reperfusion injury rats via intranasal administration, Brain Res., 1726, 10.1016/j.brainres.2019.146503 · DOI
- Jiang, 2017, Breviscapine reduces neuronal injury caused by traumatic brain injury insult: partly associated with suppression of interleukin-6 expression, Neural Regen. Res., 12, 90, 10.4103/1673-5374.198990 · DOI
- Tang, 2005, Protective effects of Breviscapine injection against focal cerebral ischemia-reperfusion injury in rats, Chin. J. Clin. Rehab., 9, 243
- Guo, 2014, Therapeutic time window and underlying therapeutic mechanism of breviscapine injection against cerebral ischemia/reperfusion injury in rats, J. Ethnopharmacol., 151, 660, 10.1016/j.jep.2013.11.026 · DOI
- Cao, 2017, Mechanism of Breviscapine on cerebral ischemia reperfusion injury of rats by CYP4A pathway, chin, J. Exp. Tradit. Med. Form., 23, 101
- Zhang, 2017, Breviscapine confers a neuroprotective efficacy against transient focal cerebral ischemia by attenuating neuronal and astrocytic autophagy in the penumbra, Biomed. Pharmacother., 90, 69, 10.1016/j.biopha.2017.03.039 · DOI
- Shi, 2009, Comparative study on the effects of breviscapine on experimental cerebral ischemia in rats, Chin. Tradit. Herbal Drugs., 40, 274
- Tao, 2013, HP-β-CD-PLGA nanoparticles improve the penetration and bioavailability of puerarin and enhance the therapeutic effects on brain ischemia–reperfusion injury in rats, Naunyn Schmiedebergs Arch. Pharmacol., 386, 61, 10.1007/s00210-012-0804-5 · DOI
- Zhou, 2014, Puerarin protects brain tissue against cerebral ischemia/reperfusion injury by inhibiting the inflammatory response, Neural Regen. Res., 9, 2074, 10.4103/1673-5374.147934 · DOI
- Ling, 2018, Synergistic effects of salvianolic acid B and puerarin on cerebral ischemia reperfusion injury, Molecules, 23, 564, 10.3390/molecules23030564 · DOI
- Wang, 2014, Puerarin protected the brain from cerebral ischemia injury via astrocyte apoptosis inhibition, Neuropharmacology, 79, 282, 10.1016/j.neuropharm.2013.12.004 · DOI
- Chen, 2018, Effects of Puerarin on the expression of P-STAT3 and P53 in Hippocampus tissue of cerebral ischemia-reperfusion injury model rats, J. Hunan Univ. Chin. Med., 38, 36
- Xu, 2005, The Neuroprotection of puerarin against cerebral ischemia is associated with the prevention of apoptosis in rats, Planta Med., 71, 585, 10.1055/s-2005-871261 · DOI
- Chen, 2011, Study on pharmacokinetics of puerarin in rats following different methods of administration of Tongqiao Sanyu prescription, Chin. J. Chin. Mater. Med., 36, 2347, 10.1007/s10856-011-4401-9 · DOI
- Yu, 2011, Formulation optimization and bioavailability after oral and nasal administration in rabbits of puerarin-loaded microemulsion, J. Pharm. Sci., 100, 933, 10.1002/jps.22333 · DOI
- Li, 2013, Bioavailability and brain-targeting of puerarin by different administration routes in rats, J. Drug Deliv. Sci. Technol., 23, 583, 10.1016/S1773-2247(13)50088-8 · DOI
- Zhang, 2016, Puerarin transport across a Calu-3 cell monolayer–an in vitro model of nasal mucosa permeability and the influence of paeoniflorin and menthol, Drug Des. Devel. Ther., 10, 2227, 10.2147/DDDT.S110247 · DOI
- Yang, 2018, Nose-to-brain delivery: puerarin uptake on olfactory ensheathing cells and transport on Calu-3 cells, Chin. J. Trad. Chin. Med. Pharm., 33, 2159
- Pei, 2016, Quercetin ameliorates ischemia/reperfusion-induced cognitive deficits by inhibiting ASK1/JNK3/caspase-3 by enhancing the Akt signaling pathway, Biochem. Biophys. Res. Commun., 478, 199, 10.1016/j.bbrc.2016.07.068 · DOI
- Chirumbolo, 2019, Quercetin Might Promote Autophagy in a Middle Cerebral Artery Occlusion-Mediated Ischemia Model: Comments on Fawad-Ali Shah et al, Neurochem. Res., 44, 297, 10.1007/s11064-018-2692-7 · DOI
- Ahmad, 2018, Intranasal delivery of quercetin-loaded mucoadhesive nanoemulsion for treatment of cerebral ischaemia, Artif. Cells Nanomed. Biotechnol., 46, 717, 10.1080/21691401.2017.1337024 · DOI
- Guo, 1983, Tetramethylpyrazine in the treatment of cardiovascular and cerebrovascular diseases, Planta Med., 47, 89, 10.1055/s-2007-969959 · DOI
- Tan, 2015, Ligustrazine reduces blood-brain barrier permeability in a rat model of focal cerebral ischemia and reperfusion, Exp. Ther. Med., 1757, 10.3892/etm.2015.2365 · DOI
- Liu, 2013, Influence of nasal tetramethylpyrazine phosphate pH-Sensitive in situ gel on amino acid content in rats brain of acute cerebral ischemia model, Chin. J. Mod. Appl. Pharm., 30, 929
- Li, 2008, Studies on brain pharmacokineties of tetramethylpyrazine hydrochloride after intranasal administration in rats, Chin. Pharm. J., 43, 452
- Meng, 2014, Comparative pharmacokinetics of tetramethylpyrazine phosphate in rat plasma and extracellular fluid of brain after intranasal, intragastric and intravenous administration, Acta Pharm. Sin. B, 4, 74, 10.1016/j.apsb.2013.12.009 · DOI
- Liu, 2012, Comparison of the brain pharmacokinetics of nasal tetramethylpyrazine phosphate pH-sensitive in situ gel in normal rats and model rats, Acta Pharm. Sin. B, 47, 677
- Ding, 2012, Research progress in analysis methods and pharmacological effects of berberine, Chin. J. Pharm. Anal, 3, 1296
- Wang, 2019, Coptidis Rhizoma: A review of its traditional uses, botany, phytochemistry, pharmacology, toxicology, Pharm. Biol., 57, 193, 10.1080/13880209.2019.1577466 · DOI
- Balmukunda, 2007, Plasma and hippocampal pharmacokinetics of berberine after intravenous or intranasal administration in rats, Pharm. Biotechnol., 14, 348
- Yang, 2018, Berberine ameliorates MCAO induced cerebral Ischemia/Reperfusion injury via activation of the BDNF–TrkB–PI3K/Akt signaling pathway, Neurochem. Res., 43, 702, 10.1007/s11064-018-2472-4 · DOI
- Pang, 2018, Effect of berberine against cerebral ischemia and reperfusion involving in the methylation of PPARγ promoter, J. Chin. Pharmac. Sci., 27, 170, 10.5246/jcps.2018.03.018 · DOI
- Liu, 2018, Effect of Berberine on angiogenesis and HIF-1α/VEGF signal transduction pathway in rats with cerebral ischemia-reperfusion injury, J. Coll. Physicians Surg. Pak., 28, 753
- Jardim, 2018, Resveratrol and brain mitochondria: a review, Mol. Neurobiol., 55, 2085, 10.1007/s12035-017-0448-z · DOI
- Peng, 2013, Botany, Phytochemistry, Pharmacology, and Potential Application of Polygonum Cuspidatum Sieb.et Zucc.: A Review, J. Ethnopharmacol., 148, 729, 10.1016/j.jep.2013.05.007 · DOI
- Das, 2007, Anti-inflammatory responses of resveratrol, Inflamm. Allergy Drug Targets, 6, 168, 10.2174/187152807781696464 · DOI
- Xia, 2017, Antioxidant effects of resveratrol in the cardiovascular system, Br. J. Pharmacol., 174, 1633, 10.1111/bph.13492 · DOI
- Kraus, 2019, Resveratrol directly controls the activity of neuronal ryanodine receptors at the single-channel level, Mol. Neurobiol., 57, 422, 10.1007/s12035-019-01705-7 · DOI
- He, 2017, Resveratrol alleviates cerebral ischemia/reperfusion injury in rats by inhibiting NLRP3 inflammasome activation through Sirt1-dependent autophagy induction, Int. Immunopharmacol., 50, 208, 10.1016/j.intimp.2017.06.029 · DOI
- Abdel-Aleem, 2016, Neuroprotective effect of resveratrol against brain ischemia reperfusion injury in rats entails reduction of DJ-1 protein expression and activation of PI3K/Akt/GSK3b survival pathway, Arch. Physiol. Biochem., 122, 200, 10.1080/13813455.2016.1182190 · DOI
- Chang, 2018, Resveratrol protects hippocampal neurons against cerebral ischemia-reperfusion injury via modulating JAK/ERK/STAT signaling pathway in rats, J. Neuroimmunol., 315, 9, 10.1016/j.jneuroim.2017.11.015 · DOI
- Pandareesh, 2015, Bioavailability of dietary polyphenols: factors contributing to their clinical application in CNS diseases, Neurochem. Int., 89, 198, 10.1016/j.neuint.2015.07.003 · DOI
- Hao, 2016, Fabrication of an ionic-sensitive in situ gel loaded with resveratrol nanosuspensions intended for direct nose-to-brain delivery, Colloids Surf. B Biointerfaces, 147, 376, 10.1016/j.colsurfb.2016.08.011 · DOI
- Wang, 2016, Salvianolic acid B ameliorates cerebral ischemia/reperfusion injury through inhibiting TLR4/MyD88 signaling pathway, Inflammation, 39, 1503, 10.1007/s10753-016-0384-5 · DOI
- Fan, 2018, Mechanism of salvianolic acid B neuroprotection against ischemia/reperfusion induced cerebral injury, Brain Res., 679, 125, 10.1016/j.brainres.2017.11.027 · DOI
- Xu, 2017, Neuroprotective effect of salvianolic acid B against cerebral ischemic injury in rats via the CD40/NF-κB pathway associated with suppression of platelets activation and neuroinflammation, Brain Res., 1661, 37, 10.1016/j.brainres.2017.02.011 · DOI
- Du, 2017, Study on nasal absorption in situ and blood-brain barrier cells absorption of SalB-LCN in vitro, Chin. J. Tradit. Chin. Med. Pharm., 32, 3140
- Ju, 2017, Effect of salvianolic acid B by intranasal administration on cognitive function and neurogenesis of cerebral ischemia rats, Chin. Tradit. Herbal Drugs., 48, 2481
- Nabavi, 2015, Curcumin: a natural product for diabetes and its complications, Curr. Top. Med. Chem., 15, 2445, 10.2174/1568026615666150619142519 · DOI
- Pluta, 2018, Neuroprotective and neurological/cognitive enhancement effects of curcumin after brain ischemia injury with Alzheimer’s disease phenotype, Int. J. Mol. Sci., 19, 4002, 10.3390/ijms19124002 · DOI
- Zhang, 2018, Curcumin attenuates cerebral ischemia injury in Sprague–Dawley rats and PC12 cells by suppressing overactivated autophagy, J. Photochem. Photobiol. B, 184, 1, 10.1016/j.jphotobiol.2018.05.010 · DOI
- Lei, 2010, Effects of curcumin on inflammatory reaction and blood-brain barrier permeability in rats following cerebral ischemic injury, Chin. Pharmacol. Bull., 26, 120
- Vaz, 2017, Cristiana Lima dora, development of nasal lipid nanocarriers containing curcumin for brain targeting, J. Alzheimers Dis., 59, 961, 10.3233/JAD-160355 · DOI
- Subhashini, 2013, Intranasal curcumin and its evaluation in murine model of asthma, Int. Immunopharmacol., 17, 733, 10.1016/j.intimp.2013.08.008 · DOI
- Long, 2018, Klotho upregulation contributes to the neuroprotection of ligustilide against cerebral ischemic injury in mice, Eur. J. Pharmacol., 820, 198, 10.1016/j.ejphar.2017.12.019 · DOI
- Yang, 2012, Advances in studies on pharmacological functions of Ligustilide and their mechanisms, Chin. Herbal Med., 4, 26
- Kuang, 2006, Neuroprotective role of Z-ligustilide against forebrain ischemic injury in ICR mice, Brain Res., 1102, 145, 10.1016/j.brainres.2006.04.110 · DOI
- Zhang, 2016, (Z)-ligustilide increases ferroportin1 expression and ferritin content in ischemic SH-SY5Y cells, Eur. J. Pharmacol., 792, 48, 10.1016/j.ejphar.2016.10.029 · DOI
- Kuang, 2014, Ligustilide ameliorates neuroinflammation and brain injury in focal cerebral ischemia/reperfusion rats: involvement of inhibition of TLR4/peroxiredoxin 6 signaling, Free Radic. Biol. Med., 71, 165, 10.1016/j.freeradbiomed.2014.03.028 · DOI
- Guo, 2013, Analgesic activity of DaChuanXiong Fang after itranasal administration and its potential active components in vivo, J. Ethnopharmacol., 150, 649, 10.1016/j.jep.2013.09.020 · DOI
- Wu, 2016, Effect of cimicifugoside H-1 on amino acid neurotransmitters in striatum of rats with cerebral ischemia, Chin. J. Pathophysiol., 32, 831
- Wu, 2016, Feasibility of nasal brain targeted drug delivery through the nose-brain channel in the nasal olfactory region using cimicifugoside H-1, J. Clin. Rehabil. Tis. Eng. Res., 20, 688
- Song, 2014, Geniposide plays an anti-inflammatory role via regulating TLR4 and downstream signaling pathways in lipopolysaccharide-induced mastitis in mice, Inflammation, 37, 1588, 10.1007/s10753-014-9885-2 · DOI
- Li, 2019, Geniposide protects against hypoxia/reperfusion-induced blood-brain barrier impairment by increasing tight junction protein expression and decreasing inflammation, oxidative stress, and apoptosis in an in vitro system, Eur. J. Pharmacol., 854, 224, 10.1016/j.ejphar.2019.04.021 · DOI
- Shen, 2017, Investigate mechanism of Dioscin and Geniposide on inflammatory of cerebral ischemia and reperfusion injury at different time points of acute phase in rats, Shaanxi J. Tradit. Chin. Med., 38, 531
- Wu, 2019, Network pharmacology identification of mechanisms of cerebral ischemia injury amelioration by Baicalin and Geniposide, Eur. J. Pharmacol., 859, 10.1016/j.ejphar.2019.172484 · DOI
- Lu, 2012, Bioavailability and brain-targeting of geniposide in gardenia-borneol co-compound by different administration routes in mice, Int. J. Mol. Sci., 13, 14127, 10.3390/ijms131114127 · DOI
- Lu, 2011, Enhancing effect of natural borneol on the absorption of geniposide in rat via intranasal administration, J. Zhejiang Univ. Sci. B, 12, 143, 10.1631/jzus.B1000121 · DOI
- Chen, 2014, Enhancing effect of borneol and muscone on geniposide transport across the human nasal epithelial cell monolayer, PLoS One, 9
- Jiang, 2016, Review on mechanisms of Panax notoginseng saponins against ischemia-reperfusion injury, Chin. Archi. Tradit. Chin. Med., 34, 267
- Tang, 2010, Effect of Panax notoginseng saponins on extracellular matrix damage and oxidative stress after cerebral ischemia - reperfusion in mice, Chin. Archi. Tradit. Chin. Med., 28, 2327
- Tang, 2011, Neuroprotective role of Panax notoginseng saponins on cerebral ischemia-reperfusion injury in rats, Chin. J. Exp. Tradi.t Med. Formul., 17, 210
- Li, 2009, Total saponins of Panax notoginseng modulate the expression of caspases and attenuate apoptosis in rats following focal cerebral ischemia-reperfusion, J. Ethnopharmacol., 121, 412, 10.1016/j.jep.2008.10.042 · DOI
- Hu, 2018, Panax notoginseng saponins protect cerebral microvascular endothelial cells against oxygen-glucose Deprivation/Reperfusion-Induced barrier dysfunction via activation of PI3K/Akt/Nrf2 antioxidant signaling pathway, Molecules, 23, 10.3390/molecules23112781 · DOI
- Wu, 2019, Panax notoginseng saponins ameliorate leukocyte adherence and cerebrovascular endothelial barrier breakdown upon ischemia-reperfusion in mice, J. Vasc. Res., 56, 1, 10.1159/000494935 · DOI
- Han, 2006, Mechanism of oral absorption of panaxnotoginseng saponins, Acta. Pharm. Sin., 41, 498
- Shen, 2004, Panax notoginseng saponin liposomes: characterization of pharmaceutics and pharmacokinetics on pulmonary instillation in rats, Chin. Tradit. Herbal Drugs., 35, 745
- Xu, 2003, Studies on formulations of Panax notoginsenosides for intranasal administration, Acta. Pharm. Sin., 38, 859
- Ding, 2015, W/O nanoemulsion-based intranasal drug delivery system of Panax notoginseng saponins for brain targeting, J. Control. Release, 213, e11, 10.1016/j.jconrel.2015.05.014 · DOI
- Liu, 2018, Ginsenoside Rb1 administration attenuates focal cerebral ischemic reperfusion injury through inhibition of HMGB1 and inflammation signals, Exp. Ther. Med., 16, 3020
- Cheng, 2019, Neuroprotective effects of ginsenosides against cerebral ischemia, Molecules, 24, 1102, 10.3390/molecules24061102 · DOI
- Zheng, 2019, Ginsenoside Rg1 attenuates protein aggregation and inflammatory response following cerebral ischemia and reperfusion injury, Eur. J. Pharmacol., 853, 65, 10.1016/j.ejphar.2019.02.018 · DOI
- Chu, 2019, Ginsenoside Rg1 protects against ischemic/reperfusion-induced neuronal injury through miR-144/Nrf2/ARE pathway, Acta Pharmacol. Sin., 40, 13, 10.1038/s41401-018-0154-z · DOI
- Cao, 2015, Pharmacokinetics and brain distribution studies of ginsenoside Rd to rats via intranasal administration by LC-MS/MS, Anal. Methods, 7, 8809, 10.1039/C5AY01750E · DOI
- Long, 2019, Gastrodin attenuates neuroinflammation in DOI-induce Tourette syndrome in rats, J. Biochem. Mol.Toxicol., 33, 10.1002/jbt.22302 · DOI
- Nie, 2010, Protective effects of gastrodine on focal cerebral ischemia reperfusion injury in rats, West China J. Pharm. Sci., 25, 423
- Yang, 2018, The therapeutic effects of novel gastrodin derivative on cerebral ischemia / reperfusion injury in rats and safety evaluation, Nat. Prod. Res. Dev., 30, 1427
- Illum, 2003, Nasal drug delivery-possibilities, problems and solutions, J. Control. Release, 87, 187, 10.1016/S0168-3659(02)00363-2 · DOI
- Cai, 2008, Brain targeting of gastrodin nasal in situ gel, J. Sichuan Univ. (Med. Sci. Ed.), 39, 438
- Shi, 2017, Study of nasal absorption characteristics of Gastrodin, Chin. J. Mod. Appl. Pharm., 34, 311
- Pan, 2018, Intranasal delivery of α-asarone to the brain with lactoferrin-modified mPEG-PLA nanoparticles prepared by premix membrane emulsification, Drug Deliv. Transl. Res., 8, 83, 10.1007/s13346-017-0438-8 · DOI
- Lu, 2014, Distribution of α-asarone in brain following three different routes of administration in rats, Eur. J. Pharm. Sci., 63, 63, 10.1016/j.ejps.2014.06.006 · DOI
- Lu, 2017, Pharmacokinetics of α-asarone after intranasal and intravenous administration with PLA-α-asarone nanoparticles, China J. Chin. Mater. Med., 42, 2366
- Yang, 2013, Beta-asarone, a major component of Acorus tatarinowii Schott, attenuates focal cerebral ischemia induced by middle cerebral artery occlusion in rats, BMC Complement. Altern. Med., 13, 236, 10.1186/1472-6882-13-236 · DOI
- Liu, 2012, Beta-asarone attenuates ischemia-reperfusion-induced autophagy in rat brains via modulating JNK, p-JNK, Bcl-2 and Beclin 1, Eur. J. Pharmacol., 680, 34, 10.1016/j.ejphar.2012.01.016 · DOI
- Zhang, 2016, Protective effects of mangiferin on cerebral ischemia-reperfusion injury and its mechanisms, Eur. J. Pharmacol., 771, 145, 10.1016/j.ejphar.2015.12.003 · DOI · Paper page
- Zhan, 2005, Effects of isoliquiritigenin on cognition dysfunction and brain energy metabolism following repeated cerebral ischemia-reperfusion in mice, Chin. Pharmacol. Bull., 21, 213
- Liang, 2014, Formononetin mediates neuroprotection against cerebral ischemia/reperfusion in rats via downregulation of the Bax/Bcl-2 ratio and upregulation PI3K/Akt signaling pathway, J. Neurol. Sci., 344, 100, 10.1016/j.jns.2014.06.033 · DOI
- Lv, 2015, Hydroxysafflor yellow A exerts neuroprotective effects in cerebral ischemia reperfusion-injured mice by suppressing the innate immune TLR4-inducing pathway, Eur. J. Pharmacol., 769, 324, 10.1016/j.ejphar.2015.11.036 · DOI
- Deng, 2018, Protective effect of hydroxysafflor yellow A alone or in combination with acetylglutamine on cerebral ischemia reperfusion injury in rat: a PET study using 18F-fuorodeoxyglucose, Eur. J. Pharmacol., 825, 119, 10.1016/j.ejphar.2018.02.011 · DOI
- Shan, 2010, Hydroxysafflor Yellow A protects spinal cords from ischemia/reperfusion injury in rabbits, BMC Neurosci., 11, 98, 10.1186/1471-2202-11-98 · DOI
- Ramagiri, 2016, Neuroprotective effect of hydroxy safflor yellow A against cerebral ischemia-reperfusion injury in rats: putative role of Mptp, J. Basic Clin. Physiol. Pharmacol., 27, 1, 10.1515/jbcpp-2015-0021 · DOI
- Zhang, 2017, Paeoniflorin attenuates cerebral ischemia-induced injury by regulating Ca2+/CaMKII/CREB signaling pathway, Molecules, 22, 10.3390/molecules22030359 · DOI
- Liu, 2012, Hyperoside protects cortical neurons from oxygen-glucose deprivation-reperfusion induced injury via nitric oxide signal pathway, Brain Res., 1469, 164, 10.1016/j.brainres.2012.06.044 · DOI
- Guo, 2012, Neuroprotective effect of calycosin on cerebral ischemia and reperfusion injury in rats, J. Ethnopharmacol., 144, 768, 10.1016/j.jep.2012.09.056 · DOI
- Guo, 2017, The role of TRPC6 in the neuroprotection of calycosin against cerebral ischemic injury, Sci. Rep., 7, 3039, 10.1038/s41598-017-03404-6 · DOI
- Wang, 2014, Downregulated RASD1 and upregulated miR-375 are involved in protective effects of calycosin on cerebral ischemia/reperfusion rats, J. Neurol. Sci., 339, 144, 10.1016/j.jns.2014.02.002 · DOI
- Wang, 2018, Neuroprotective mechanisms of calycosin against focal cerebral ischemia and reperfusion injury in rats, Cell. Physiol. Biochem., 45, 537, 10.1159/000487031 · DOI
- Liu, 2018, Rutin attenuates cerebral ischemia/reperfusion injury in ovariectomized rats via estrogen receptor-mediated BDNF-TrkB and NGF-TrkA signaling, Biochem. Cell Biol., 96, 672, 10.1139/bcb-2017-0209 · DOI
- Khan, 2009, Rutin protects the neural damage induced by transient focal ischemia in rats, Brain Res., 1292, 123, 10.1016/j.brainres.2009.07.026 · DOI
- Wang, 2015, Vitexin protects brain against ischemia/reperfusion injury via modulating mitogen-activated protein kinase and apoptosis signaling in mice, Phytomedicine, 22, 379, 10.1016/j.phymed.2015.01.009 · DOI
- Cui, 2019, Vitexin protects against ischemia/reperfusion-induced brain endothelial permeability, Eur. J. Pharmacol., 853, 210, 10.1016/j.ejphar.2019.03.015 · DOI
- Guo, 2008, Protective effects of total flavones of rhododendra on cerebral ischemia reperfusion injury, Am. J. Chin. Med., 36, 343, 10.1142/S0192415X08005813 · DOI
- Han, 2018, Total flavone of Rhododendron Improves cerebral ischemia injury by activating vascular TRPV4 to induce endothelium-derived hyperpolarizing factor-mediated responses, Evid-Based. Compl. Alt.
- Sun, 2018, Total flavones of Rhododendron simsii Planch flower protect isolated rat heart from ischaemia-reperfusion injury and its mechanism of UTR-RhoA-ROCK pathway inhibition, J. Pharm. Pharmacol., 70, 1713, 10.1111/jphp.13016 · DOI
- Yu, 2009, Protective effects of total flavones of rhododendra against global cerebral ischemia reperfusion injury, Am. J. Chin. Med., 37, 877, 10.1142/S0192415X09007284 · DOI
- Pang, 2018, Apigenin protects the brain against Ischemia/Reperfusion injury via Caveolin-1/VEGF in vitro and in vivo, Oxid. Med. Cell. Longev.
- Yang, 2016, Therapeutic effect analysis of Sinomenine on rat cerebral ischemia–Reperfusion injury, J. Stroke Cerebrovasc. Dis., 25, 1263, 10.1016/j.jstrokecerebrovasdis.2016.02.023 · DOI
- Li, 2012, Protective effects of Sinomenine on mice brain cells after ischemia-reperfusion injury, Med. Res. Educ., 29, 14
- Zhou, 2009, Effect of Sinomenine on expression of Bcl-2 and Bax following cerebral ischemic reperfusion injury in diabetic rats, J. Emerg. Tradit. Chin. Med., 18, 763
- Chen, 2010, Effects of Matrine on inflammatory cytokines for rats with cerebral ischemia reperfusion injury, J. Emerg. Tradit. Chin. Med., 19, 2098
- Zhao, 2015, Matrine attenuates focal cerebral ischemic injury by improving antioxidant activity and inhibiting apoptosis in mice, Int. J. Mol. Med., 36, 633, 10.3892/ijmm.2015.2260 · DOI
- Chen, 2012, Neuroprotection of tanshinone IIA against cerebral ischemia/reperfusion injury through inhibition of macrophage migration inhibitory factor in rats, PLoS One, 7, 10.1371/journal.pone.0040165 · DOI
- Tang, 2014, Protective effect of tanshinone IIA on the brain and its therapeutic time window in rat models of cerebral ischemia-reperfusion, Exp. Ther. Med., 8, 1616, 10.3892/etm.2014.1936 · DOI
- Li, 2015, Studies on the active constituents in radix salviae miltiorrhizae and their protective effects on cerebral ischemia reperfusion injury and its mechanism, Pharmacogn. Mag., 11, 69, 10.4103/0973-1296.149706 · DOI
- Cai, 2017, Tanshinone IIA elicits neuroprotective effect through activating the nuclear factor erythroid 2-Related factor-dependent antioxidant response, Rejuvenation Res., 20, 286, 10.1089/rej.2016.1912 · DOI
- Wen, 2016, Tanshinone IIA increases levels of NeuN, protein disulfide isomerase, and Na+/K+-ATPase and decreases evidence of microglial activation after cerebral ischemic injury, Neuroreport, 27, 435, 10.1097/WNR.0000000000000559 · DOI
- Zhang, 2016, Ilexonin a promotes neuronal proliferation and regeneration via activation of the canonical wnt signaling pathway after cerebral ischemia reperfusion in rats, Evid. Complement. Alternat. Med., 2016
- Xu, 2016, Neuroprotective effects of Ilexonin A following transient focal cerebral ischemia in rats, Mol. Med. Rep., 13, 957, 10.3892/mmr.2016.4921 · DOI
- Guo, 2010, Anti-inflammation effects of picroside 2 in cerebral ischemic injury rats, Behav. Brain Funct., 6, 43, 10.1186/1744-9081-6-43 · DOI · Paper page
- Li, 2018, Picroside II exerts a neuroprotective effect by inhibiting mPTP permeability and EndoG release after cerebral Ischemia/Reperfusion injury in rats, J. Mol. Neurosci., 64, 144, 10.1007/s12031-017-1012-z · DOI
- Wang, 2015, Picroside II inhibits the MEK-ERK1/2-COX2 signal pathway to prevent cerebral ischemic injury in rats, J. Mol. Neurosci., 57, 335, 10.1007/s12031-015-0623-5 · DOI · Paper page
- Zhang, 2017, Picroside II exerts a neuroprotective effect by inhibiting the mitochondria cytochrome C signal pathway following ischemia reperfusion injury in rats, J. Mol. Neurosci., 61, 267, 10.1007/s12031-016-0870-0 · DOI
- Liu, 2016, Morroniside promotes angiogenesis and further improves microvascular circulation after focal cerebral ischemia/reperfusion, Brain Res, Bull., 127, 111
- Wang, 2010, Neuroprotective effect of morroniside on focal cerebral ischemia in rats, Brain Res. Bull., 83, 196, 10.1016/j.brainresbull.2010.07.003 · DOI
- Zeng, 2018, Morroniside protects against cerebral ischemia/reperfusion injury by inhibiting neuron apoptosis and MMP2/9 expression, Exp. Ther. Med., 16, 2229
- Gu, 2012, Inhibition of NF-κB activation is associated with anti-inflammatory and anti-apoptotic effects of Ginkgolide B in a mouse model of cerebral ischemia/reperfusion injury, Eur. J. Pharm. Sci., 47, 652, 10.1016/j.ejps.2012.07.016 · DOI
- Zheng, 2018, Ginkgolide B promotes the proliferation and differentiation of neural stem cells following cerebral ischemia/reperfusion injury, both in vivo and in vitro, Neural Regen, Res., 13, 1204
- Ma, 2012, Neuroprotective effect of ginkgolide K against acute ischemic stroke on middle cerebral ischemia occlusion in rats, J. Nat. Med., 66, 25, 10.1007/s11418-011-0545-7 · DOI
- Liu, 2019, Antioxidant effects of ginkgolides and bilobalide against cerebral ischemia injury by activating the Akt/Nrf2 pathway in vitro and in vivo, Cell Stress Chaperones, 24, 441, 10.1007/s12192-019-00977-1 · DOI
- Zheng, 2018, By activating Akt/eNOS bilobalide B inhibits autophagy and promotes angiogenesis following focal cerebral ischemia reperfusion, Cell. Physiol. Biochem., 47, 604, 10.1159/000490016 · DOI
- Yuan, 2017, Effects of artemisinin on expression of apoptosis-related factors and inflammatory mediators, Contemp. Med., 23, 23
- Mao, 2011, Osthole, a natural coumarin, improves neurobehavioral functions and reduces infarct volume and matrix metalloproteinase-9 activity after transient focal cerebral ischemia in rats, Brain Res., 1385, 275, 10.1016/j.brainres.2011.02.015 · DOI
- Ling, 2008, The protective effect of Chuanxiong Oil on focal cerehral reperfusion injury in rat, Pharmaco. Clin. Chin. Materia Medica., 24, 39
- Wei, 2017, Salidroside inhibits inflammation through PI3K/Akt/HIF signaling after focal cerebral ischemia in rats, Inflammation, 40, 1, 10.1007/s10753-017-0573-x · DOI
- Yin, 2010, Protective effect of astragaloside on focal cerebral Ischemia/Reperfusion injury in rats, Am. J. Chin. Med., 38, 517, 10.1142/S0192415X10008020 · DOI
- Yin, 2009, Effects of astragalosides on the expression of BDNF, TrkB and p75NTR mRNA against focal cerebral ischemia-reperfusion injury, Chin. Pharmacol. Bull., 25, 672
- Wu, 2014, Astragalosides attenuate learning and memory impairment in rats following ischemia reperfusion injury, Mol. Med. Rep., 9, 1319, 10.3892/mmr.2014.1969 · DOI
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Zeng, J., Bao, T., Yang, K., Zhu, X., Wang, S., Xiang, W., Ge, A., Zeng, L., & Ge, J. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1047550 · Cited by 175
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Self-citationCheng, Y., Gai, C., Zhao, Y., Li, T., Song, Y., Luo, Q., Xin, D., Jiang, Z., Chen, W., Liu, D., et al. (2025) · Neuroscience Bulletin · doi:10.1007/s12264-025-01376-6 · Cited by 5
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Metadata
- Authors
- Long, Y., Yang, Q., Xiang, Y., Zhang, Y., Wan, J., Liu, S., Li, N., & Peng, W.
- Venue
- Pharmacological Research
- Publisher
- Elsevier BV
- Published
- 2020-09
- Volume
- 159
- Pages
- 104795
- ISSN
- 1043-6618
- Cited by
- 151
- References
- 8
- Language
- en
- Funders
- National Natural Science Foundation of China
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