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Differences in the antinociceptive effects of serotonin-noradrenaline reuptake inhibitors via sodium channel blockade using the veratrine test in mice.

Neuroreport

Yoshizawa K, Suzuki Y, Nakamura T, Takahashi Y, Makino K, Takahashi H.
PMID: 33994525
Neuroreport. 2021 Jun 09;32(9):797-802. doi: 10.1097/WNR.0000000000001658.

Antidepressants exert their analgesic effects by inhibiting the reuptake of noradrenaline. Several antidepressants have been shown to block the sodium channels, which might contribute to their analgesic potency. The aim of this study was to determine whether serotonin-noradrenaline reuptake...

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Yoshizawa K, Suzuki Y, Nakamura T, et al. Differences in the antinociceptive effects of serotonin-noradrenaline reuptake inhibitors via sodium channel blockade using the veratrine test in mice. Neuroreport. 2021;32(9):797-802doi: 10.1097/WNR.0000000000001658.
Yoshizawa, K., Suzuki, Y., Nakamura, T., Takahashi, Y., Makino, K., & Takahashi, H. (2021). Differences in the antinociceptive effects of serotonin-noradrenaline reuptake inhibitors via sodium channel blockade using the veratrine test in mice. Neuroreport, 32(9), 797-802. https://doi.org/10.1097/WNR.0000000000001658
Yoshizawa, Kazumi, et al. "Differences in the antinociceptive effects of serotonin-noradrenaline reuptake inhibitors via sodium channel blockade using the veratrine test in mice." Neuroreport vol. 32,9 (2021): 797-802. doi: https://doi.org/10.1097/WNR.0000000000001658
Yoshizawa K, Suzuki Y, Nakamura T, Takahashi Y, Makino K, Takahashi H. Differences in the antinociceptive effects of serotonin-noradrenaline reuptake inhibitors via sodium channel blockade using the veratrine test in mice. Neuroreport. 2021 Jun 09;32(9):797-802. doi: 10.1097/WNR.0000000000001658. PMID: 33994525.
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Extraction and Chemical Characterization of Functional Phenols and Proteins from Coffee (.

Biomolecules

Prandi B, Ferri M, Monari S, Zurlini C, Cigognini I, Verstringe S, Schaller D, Walter M, Navarini L, Tassoni A, Sforza S, Tedeschi T.
PMID: 34827569
Biomolecules. 2021 Oct 22;11(11). doi: 10.3390/biom11111571.

Not all the coffee produced goes to the roasting stage, because non-compliant green coffee beans are usually discarded by roasters and the silverskin of the coffee is usually removed and discarded. In the present work, non-compliant green coffee beans...

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Prandi B, Ferri M, Monari S, et al. Extraction and Chemical Characterization of Functional Phenols and Proteins from Coffee (. Biomolecules. 2021;11(11)doi: 10.3390/biom11111571.
Prandi, B., Ferri, M., Monari, S., Zurlini, C., Cigognini, I., Verstringe, S., Schaller, D., Walter, M., Navarini, L., Tassoni, A., Sforza, S., & Tedeschi, T. (2021). Extraction and Chemical Characterization of Functional Phenols and Proteins from Coffee (. Biomolecules, 11(11), . https://doi.org/10.3390/biom11111571
Prandi, Barbara, et al. "Extraction and Chemical Characterization of Functional Phenols and Proteins from Coffee (." Biomolecules vol. 11,11 (2021). doi: https://doi.org/10.3390/biom11111571
Prandi B, Ferri M, Monari S, Zurlini C, Cigognini I, Verstringe S, Schaller D, Walter M, Navarini L, Tassoni A, Sforza S, Tedeschi T. Extraction and Chemical Characterization of Functional Phenols and Proteins from Coffee (. Biomolecules. 2021 Oct 22;11(11). doi: 10.3390/biom11111571. PMID: 34827569; PMCID: PMC8615506.
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STABILIZATION OF SPIDER CRAB NERVE MEMBRANES BY ALKALINE EARTHS, AS MANIFESTED IN RESTING POTENTIAL MEASUREMENTS.

The Journal of general physiology

Guttman R.
PMID: 19873160
J Gen Physiol. 1940 Jan 20;23(3):343-64. doi: 10.1085/jgp.23.3.343.

1. The alkaline earths, Ba, Sr, Ca, and Mg, in isotonic solutions of their chlorides, have, in general, no effect upon the resting potential of non-medullated spider crab nerve. 2. Ba, Sr, and Ca can, however, prevent the depressing...

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Guttman R. STABILIZATION OF SPIDER CRAB NERVE MEMBRANES BY ALKALINE EARTHS, AS MANIFESTED IN RESTING POTENTIAL MEASUREMENTS. J Gen Physiol. 1940;23(3):343-64doi: 10.1085/jgp.23.3.343.
Guttman, R. (1940). STABILIZATION OF SPIDER CRAB NERVE MEMBRANES BY ALKALINE EARTHS, AS MANIFESTED IN RESTING POTENTIAL MEASUREMENTS. The Journal of general physiology, 23(3), 343-64. https://doi.org/10.1085/jgp.23.3.343
Guttman, R. "STABILIZATION OF SPIDER CRAB NERVE MEMBRANES BY ALKALINE EARTHS, AS MANIFESTED IN RESTING POTENTIAL MEASUREMENTS." The Journal of general physiology vol. 23,3 (1940): 343-64. doi: https://doi.org/10.1085/jgp.23.3.343
Guttman R. STABILIZATION OF SPIDER CRAB NERVE MEMBRANES BY ALKALINE EARTHS, AS MANIFESTED IN RESTING POTENTIAL MEASUREMENTS. J Gen Physiol. 1940 Jan 20;23(3):343-64. doi: 10.1085/jgp.23.3.343. PMID: 19873160; PMCID: PMC2237927.
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Tetanus toxin treatment in vitro inhibits the release of GABA from rat cerebral cortex slices evoked by high K(+) and Na(+)-free media.

Neurochemistry international

Heredero J, Korpi ER, Oja SS.
PMID: 20487934
Neurochem Int. 1983;5(1):137-43. doi: 10.1016/0197-0186(83)90020-7.

The influence of tetanus toxin in vitro on the release of exogenous [(3)H]GABA was studied with rat cerebral cortex slices. The influx, long-term accumulation and spontaneous efflux of GABA were not modified by the toxin. The release induced by...

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Heredero J, Korpi ER, Oja SS. Tetanus toxin treatment in vitro inhibits the release of GABA from rat cerebral cortex slices evoked by high K(+) and Na(+)-free media. Neurochem Int. 1983;5(1):137-43doi: 10.1016/0197-0186(83)90020-7.
Heredero, J., Korpi, E. R., & Oja, S. S. (1983). Tetanus toxin treatment in vitro inhibits the release of GABA from rat cerebral cortex slices evoked by high K(+) and Na(+)-free media. Neurochemistry international, 5(1), 137-43. https://doi.org/10.1016/0197-0186(83)90020-7
Heredero, J, et al. "Tetanus toxin treatment in vitro inhibits the release of GABA from rat cerebral cortex slices evoked by high K(+) and Na(+)-free media." Neurochemistry international vol. 5,1 (1983): 137-43. doi: https://doi.org/10.1016/0197-0186(83)90020-7
Heredero J, Korpi ER, Oja SS. Tetanus toxin treatment in vitro inhibits the release of GABA from rat cerebral cortex slices evoked by high K(+) and Na(+)-free media. Neurochem Int. 1983;5(1):137-43. doi: 10.1016/0197-0186(83)90020-7. PMID: 20487934.
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Depolarization-induced release of [(3)H]histamine by high potassium concentrations, electrical stimulation and veratrine from rat brain slices after incubation with the radiolabelled amine.

Neurochemistry international

Mulder AH, van Amsterdam RG, Wilbrink M, Schoffelmeer AN.
PMID: 20487952
Neurochem Int. 1983;5(3):291-7. doi: 10.1016/0197-0186(83)90031-1.

Brain slices obtained from neocortex, hypothalamus or hippocampus were incubated with [(3)H]histamine and subsequently superfused and exposed to different depolarizing stimuli, viz. high K(+)-concentrations, electrical field stimulation and veratrine. K(+)-induced release of tritium was completely calcium-dependent and its magnitude...

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Mulder AH, van Amsterdam RG, Wilbrink M, et al. Depolarization-induced release of [(3)H]histamine by high potassium concentrations, electrical stimulation and veratrine from rat brain slices after incubation with the radiolabelled amine. Neurochem Int. 1983;5(3):291-7doi: 10.1016/0197-0186(83)90031-1.
Mulder, A. H., van Amsterdam, R. G., Wilbrink, M., & Schoffelmeer, A. N. (1983). Depolarization-induced release of [(3)H]histamine by high potassium concentrations, electrical stimulation and veratrine from rat brain slices after incubation with the radiolabelled amine. Neurochemistry international, 5(3), 291-7. https://doi.org/10.1016/0197-0186(83)90031-1
Mulder, A H, et al. "Depolarization-induced release of [(3)H]histamine by high potassium concentrations, electrical stimulation and veratrine from rat brain slices after incubation with the radiolabelled amine." Neurochemistry international vol. 5,3 (1983): 291-7. doi: https://doi.org/10.1016/0197-0186(83)90031-1
Mulder AH, van Amsterdam RG, Wilbrink M, Schoffelmeer AN. Depolarization-induced release of [(3)H]histamine by high potassium concentrations, electrical stimulation and veratrine from rat brain slices after incubation with the radiolabelled amine. Neurochem Int. 1983;5(3):291-7. doi: 10.1016/0197-0186(83)90031-1. PMID: 20487952.
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Observations on striated muscles of Bufo vulgaris perfused with monobromoacetic acid and on the action of atropine and veratrine on said muscles.

Archivio di scienze biologiche

LAPORTA, SAVIANO, LAPORTA G.
PMID: 18101405
Arch Sci Biol (Bologna). 1948 Jul-Aug;32(5):305-20.

No abstract available.

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LAPORTA, SAVIANO, LAPORTA G. Osservazioni su muscoli striati di Bufo vulgaris perfusi con acido monobromoacetico e sull'azione dell'atropina e della veratrina su detti muscoli. Observations on striated muscles of Bufo vulgaris perfused with monobromoacetic acid and on the action of atropine and veratrine on said muscles. Arch Sci Biol (Bologna). 1948;32(5):305-20
LAPORTA, SAVIANO, & LAPORTA, G. (1948). Osservazioni su muscoli striati di Bufo vulgaris perfusi con acido monobromoacetico e sull'azione dell'atropina e della veratrina su detti muscoli. Observations on striated muscles of Bufo vulgaris perfused with monobromoacetic acid and on the action of atropine and veratrine on said muscles. Archivio di scienze biologiche, 32(5), 305-20.
LAPORTA, et al. "Osservazioni su muscoli striati di Bufo vulgaris perfusi con acido monobromoacetico e sull'azione dell'atropina e della veratrina su detti muscoli." Observations on striated muscles of Bufo vulgaris perfused with monobromoacetic acid and on the action of atropine and veratrine on said muscles. Archivio di scienze biologiche vol. 32,5 (1948): 305-20.
LAPORTA, SAVIANO, LAPORTA G. Osservazioni su muscoli striati di Bufo vulgaris perfusi con acido monobromoacetico e sull'azione dell'atropina e della veratrina su detti muscoli. Observations on striated muscles of Bufo vulgaris perfused with monobromoacetic acid and on the action of atropine and veratrine on said muscles. Arch Sci Biol (Bologna). 1948 Jul-Aug;32(5):305-20. Italian. PMID: 18101405.
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Use of FGF-21 as a Biomarker of Mitochondrial Disease in Clinical Practice.

Journal of clinical medicine

Morovat A, Weerasinghe G, Nesbitt V, Hofer M, Agnew T, Quaghebeur G, Sergeant K, Fratter C, Guha N, Mirzazadeh M, Poulton J.
PMID: 28825656
J Clin Med. 2017 Aug 21;6(8). doi: 10.3390/jcm6080080.

Recent work has suggested that fibroblast growth factor-21 (FGF-21) is a useful biomarker of mitochondrial disease (MD). We routinely measured FGF-21 levels on patients who were investigated at our centre for MD and evaluated its diagnostic performance based on...

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Morovat A, Weerasinghe G, Nesbitt V, et al. Use of FGF-21 as a Biomarker of Mitochondrial Disease in Clinical Practice. J Clin Med. 2017;6(8)doi: 10.3390/jcm6080080.
Morovat, A., Weerasinghe, G., Nesbitt, V., Hofer, M., Agnew, T., Quaghebeur, G., Sergeant, K., Fratter, C., Guha, N., Mirzazadeh, M., & Poulton, J. (2017). Use of FGF-21 as a Biomarker of Mitochondrial Disease in Clinical Practice. Journal of clinical medicine, 6(8), . https://doi.org/10.3390/jcm6080080
Morovat, Alireza, et al. "Use of FGF-21 as a Biomarker of Mitochondrial Disease in Clinical Practice." Journal of clinical medicine vol. 6,8 (2017). doi: https://doi.org/10.3390/jcm6080080
Morovat A, Weerasinghe G, Nesbitt V, Hofer M, Agnew T, Quaghebeur G, Sergeant K, Fratter C, Guha N, Mirzazadeh M, Poulton J. Use of FGF-21 as a Biomarker of Mitochondrial Disease in Clinical Practice. J Clin Med. 2017 Aug 21;6(8). doi: 10.3390/jcm6080080. PMID: 28825656; PMCID: PMC5575582.
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Affect Intensity Moderates the Association of Emotional Clarity with Emotion Regulation and Depressive Symptoms in Unselected and Treatment-Seeking Samples.

Cognitive therapy and research

Vine V, Marroquín B.
PMID: 29657347
Cognit Ther Res. 2018 Feb;42(1):1-15. doi: 10.1007/s10608-017-9870-9. Epub 2017 Sep 21.

Depression is associated with subjective difficulties identifying one's emotions, known as low emotional clarity, but the mediators and moderators of this relationship are not well understood. We hypothesized that the role of emotional clarity in emotion regulation and, in...

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Vine V, Marroquín B. Affect Intensity Moderates the Association of Emotional Clarity with Emotion Regulation and Depressive Symptoms in Unselected and Treatment-Seeking Samples. Cognit Ther Res. 2017;42(1):1-15doi: 10.1007/s10608-017-9870-9.
Vine, V., & Marroquín, B. (2018). Affect Intensity Moderates the Association of Emotional Clarity with Emotion Regulation and Depressive Symptoms in Unselected and Treatment-Seeking Samples. Cognitive therapy and research, 42(1), 1-15. https://doi.org/10.1007/s10608-017-9870-9
Vine, Vera, and Marroquín, Brett. "Affect Intensity Moderates the Association of Emotional Clarity with Emotion Regulation and Depressive Symptoms in Unselected and Treatment-Seeking Samples." Cognitive therapy and research vol. 42,1 (2018): 1-15. doi: https://doi.org/10.1007/s10608-017-9870-9
Vine V, Marroquín B. Affect Intensity Moderates the Association of Emotional Clarity with Emotion Regulation and Depressive Symptoms in Unselected and Treatment-Seeking Samples. Cognit Ther Res. 2018 Feb;42(1):1-15. doi: 10.1007/s10608-017-9870-9. Epub 2017 Sep 21. PMID: 29657347; PMCID: PMC5894863.
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Potassium and veratrine-stimulated l-[(3)H]cysteine sulfinate and l-[(3)H]glutamate release from rat brain slices.

Neurochemistry international

Recasens M, Fagni L, Baudry M, Lynch G.
PMID: 20488052
Neurochem Int. 1984;6(3):325-32. doi: 10.1016/0197-0186(84)90074-3.

The release of l-[(3)H]cysteine sulfinic acid, l-[(3)H]glutamatic acid and [(3)H]GABA from preloaded slices of various rat brain regions in response to either 30 mM K(+) or veratrin was investigated. All these aminoacids were released by both depolarizing agents, which...

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Recasens M, Fagni L, Baudry M, et al. Potassium and veratrine-stimulated l-[(3)H]cysteine sulfinate and l-[(3)H]glutamate release from rat brain slices. Neurochem Int. 1984;6(3):325-32doi: 10.1016/0197-0186(84)90074-3.
Recasens, M., Fagni, L., Baudry, M., & Lynch, G. (1984). Potassium and veratrine-stimulated l-[(3)H]cysteine sulfinate and l-[(3)H]glutamate release from rat brain slices. Neurochemistry international, 6(3), 325-32. https://doi.org/10.1016/0197-0186(84)90074-3
Recasens, M, et al. "Potassium and veratrine-stimulated l-[(3)H]cysteine sulfinate and l-[(3)H]glutamate release from rat brain slices." Neurochemistry international vol. 6,3 (1984): 325-32. doi: https://doi.org/10.1016/0197-0186(84)90074-3
Recasens M, Fagni L, Baudry M, Lynch G. Potassium and veratrine-stimulated l-[(3)H]cysteine sulfinate and l-[(3)H]glutamate release from rat brain slices. Neurochem Int. 1984;6(3):325-32. doi: 10.1016/0197-0186(84)90074-3. PMID: 20488052.
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Momentary borderline personality disorder symptoms in youth as a function of parental invalidation and youth-perceived support.

Journal of child psychology and psychiatry, and allied disciplines

Vanwoerden S, Byrd AL, Vine V, Beeney JE, Scott LN, Stepp SD.
PMID: 34036585
J Child Psychol Psychiatry. 2021 May 25; doi: 10.1111/jcpp.13443. Epub 2021 May 25.

BACKGROUND: Parental invalidation is central to etiological models of borderline personality disorder (BPD). Previous studies relied on retrospective accounts or laboratory observations to examine these associations. There is a dearth of research assessing these constructs in daily life, and...

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Vanwoerden S, Byrd AL, Vine V, et al. Momentary borderline personality disorder symptoms in youth as a function of parental invalidation and youth-perceived support. J Child Psychol Psychiatry. 2021;doi: 10.1111/jcpp.13443.
Vanwoerden, S., Byrd, A. L., Vine, V., Beeney, J. E., Scott, L. N., & Stepp, S. D. (2021). Momentary borderline personality disorder symptoms in youth as a function of parental invalidation and youth-perceived support. Journal of child psychology and psychiatry, and allied disciplines, . https://doi.org/10.1111/jcpp.13443
Vanwoerden, Salome, et al. "Momentary borderline personality disorder symptoms in youth as a function of parental invalidation and youth-perceived support." Journal of child psychology and psychiatry, and allied disciplines vol. (2021). doi: https://doi.org/10.1111/jcpp.13443
Vanwoerden S, Byrd AL, Vine V, Beeney JE, Scott LN, Stepp SD. Momentary borderline personality disorder symptoms in youth as a function of parental invalidation and youth-perceived support. J Child Psychol Psychiatry. 2021 May 25; doi: 10.1111/jcpp.13443. Epub 2021 May 25. PMID: 34036585.
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Extraction and Chemical Characterization of Functional Phenols and Proteins from Coffee (.

Biomolecules

Prandi B, Ferri M, Monari S, Zurlini C, Cigognini I, Verstringe S, Schaller D, Walter M, Navarini L, Tassoni A, Sforza S, Tedeschi T.
PMID: 34827569
Biomolecules. 2021 Oct 22;11(11). doi: 10.3390/biom11111571.

Not all the coffee produced goes to the roasting stage, because non-compliant green coffee beans are usually discarded by roasters and the silverskin of the coffee is usually removed and discarded. In the present work, non-compliant green coffee beans...

Cite
Prandi B, Ferri M, Monari S, et al. Extraction and Chemical Characterization of Functional Phenols and Proteins from Coffee (. Biomolecules. 2021;11(11)doi: 10.3390/biom11111571.
Prandi, B., Ferri, M., Monari, S., Zurlini, C., Cigognini, I., Verstringe, S., Schaller, D., Walter, M., Navarini, L., Tassoni, A., Sforza, S., & Tedeschi, T. (2021). Extraction and Chemical Characterization of Functional Phenols and Proteins from Coffee (. Biomolecules, 11(11), . https://doi.org/10.3390/biom11111571
Prandi, Barbara, et al. "Extraction and Chemical Characterization of Functional Phenols and Proteins from Coffee (." Biomolecules vol. 11,11 (2021). doi: https://doi.org/10.3390/biom11111571
Prandi B, Ferri M, Monari S, Zurlini C, Cigognini I, Verstringe S, Schaller D, Walter M, Navarini L, Tassoni A, Sforza S, Tedeschi T. Extraction and Chemical Characterization of Functional Phenols and Proteins from Coffee (. Biomolecules. 2021 Oct 22;11(11). doi: 10.3390/biom11111571. PMID: 34827569; PMCID: PMC8615506.
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The heat-production and the mechanism of the veratrine contraction.

The Journal of physiology

Hartree W, Hill AV.
PMID: 16993531
J Physiol. 1922 Jul 21;56(5):294-300. doi: 10.1113/jphysiol.1922.sp002012.

No abstract available.

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Hartree W, Hill AV. The heat-production and the mechanism of the veratrine contraction. J Physiol. 1922;56(5):294-300doi: 10.1113/jphysiol.1922.sp002012.
Hartree, W., & Hill, A. V. (1922). The heat-production and the mechanism of the veratrine contraction. The Journal of physiology, 56(5), 294-300. https://doi.org/10.1113/jphysiol.1922.sp002012
Hartree, W, and Hill, A V. "The heat-production and the mechanism of the veratrine contraction." The Journal of physiology vol. 56,5 (1922): 294-300. doi: https://doi.org/10.1113/jphysiol.1922.sp002012
Hartree W, Hill AV. The heat-production and the mechanism of the veratrine contraction. J Physiol. 1922 Jul 21;56(5):294-300. doi: 10.1113/jphysiol.1922.sp002012. PMID: 16993531; PMCID: PMC1405371.
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Showing 13 to 24 of 26 entries