Mechanosensing and anesthesia of single internodal cells of Chara

References

• Leopold AC. 2014. Smart plants: Memory and communication without brains. Plant Signal Behav. 9(10):e972268. doi:10.4161/15592316.2014.972268.
   PubMedGoogle Scholar
• Trewavas A. 2021. Awareness and integrated information theory identify plant meristems as sites of conscious activity. Protoplasma. 258(3):673–7. doi:10.1007/s00709-021-01633-1.
   PubMed Web of Science ®Google Scholar
• Baluška F, Yokawa K. 2021. Anaesthetics and plants: from sensory systems to cognition-based adaptive behaviour. Protoplasma. 258(2):449–454. doi:10.1007/s00709-020-01594-x.
   PubMed Web of Science ®Google Scholar
• Eckenhoff R. 2008. Why can all of biology be anesthetized? Anesth Analg. 107(3):859–861. doi:10.1213/ane.0b013e31817ee7ee.
   PubMed Web of Science ®Google Scholar
• Pavlovič A, Libiaková M, Bokor B, Jakšová J, Petřík I, Novák O, Baluška F. 2020. Anaesthesia with diethyl ether impairs jasmonate signalling in the carnivorous plant Venus flytrap (Dionaea muscipula). Ann Bot. 125(1):173–183. doi:10.1093/aob/mcz177.
   PubMed Web of Science ®Google Scholar
• Yokawa K, Kagenishi T, Pavlovič A, Gall S, Weiland M, Mancuso S, Baluška F. 2018. Anaesthetics stop diverse plant organ movements, affect endocytic vesicle recycling and ROS homeostasis, and block action potentials in Venus flytraps. Ann Bot. 122:747–756. doi:10.1093/aob/mcx155.
   PubMed Web of Science ®Google Scholar
• Bernard C. 1878a. Lectures on phenomena of life common to animals and plants. Paris: Ballliere, and Son. https://www.google.com/books/edition/Le%C3%A7ons_sur_les_ph%C3%A9nom%C3%A8nes_de_la_vie_c/63IbM3U9jyQC?hl=en&gbpv=1&dq=Bernard+C.+Le%C3%A7onssur+les+ph%C3%A9nom%C3%A8nes+de+la+vie+communs+aux+animauxet+aux+v%C3%A9g%C3%A9taux.+Lectures+on+Phenomena+of+Life+Common+to+Animals+and+Plants.+Paris,+Ballliere,+and+Son,+1878+&pg=PR2&printsec=frontcover
   Google Scholar
• Rice NP. 1859. Trials of a public benefactor, as illustrated in the discovery of etherization. New York: Pudney & Russell; p. 137.
   Google Scholar
• Bergman N. 1992. Michael Faraday and his contribution to anesthesia. Anesthesiology. 77(4):812–816. doi:10.1097/00000542-199210000-00027.
   PubMed Web of Science ®Google Scholar
• Boote F. 1847. Surgical operations performed during insensibility produced by the inhalation of sulphuric ether. Lancet. 49:5–8.
   Google Scholar
• Rinaldi A. 2014. Reawakening anaesthesia research. EMBO Rep. 15(11):1113–1118. doi:10.15252/embr.201439593.
   PubMedGoogle Scholar
• Bernard C. 1878b. La science expérimentale. Paris: J.B. Baillière & fils.
   Google Scholar
• Staves M, Wayne R, Leopold AC. 1995. Detection of gravity-induced polarity of cytoplasmic streaming in Chara. Protoplasma. 188(1–2):38–48. doi:10.1007/BF01276794.
   PubMed Web of Science ®Google Scholar
• Kikuyama M. 2001. Role of Ca2+ in membrane excitation and cell motility in characean cells as a model system. Int Rev Cytol. 201:85–114.
   PubMedGoogle Scholar
• Engelmann W. 1884. Die protoplasmabewegung (physiology of protoplasmic movement). J Cell Sci. 2-24(95):370–418. doi:10.1242/jcs.s2-24.95.370.
   Google Scholar
• Ewart AJ. 1903. On the physics and physiology of protoplasmic streaming in plants. Oxford: Clarendon Press; p. 131.
   Google Scholar
• Hörmann G. 1898; Studien uiber die Protoplasmastromung bei den Characeen. 79. Jena: Fischer.
   Google Scholar
• Kaneko T, Saito C, Shimmen T, Kikuyam M. 2005. Possible involvement of mechanosensitive Ca2+ channels of plasma membrane in mechanoperception in Chara. Plant Cell Physiol. 46(1):130–135. doi:10.1093/pcp/pci004.
   PubMed Web of Science ®Google Scholar
• Kaneko T, Takahashi N, Kikuyama M. 2009. Membrane stretching triggers mechanosensitive Ca2+ channel activation in Chara. J Membr Biol. 228(1):33–42. doi:10.1007/s00232-009-9156-6.
   PubMed Web of Science ®Google Scholar
• Kishimoto U. 1968. Response of Chara internodes to mechanical stimulation. Annual report of the biology works of the faculty of science. Osaka Univ. 16:61–66.
   Google Scholar
• Staves M, Wayne R. 1993. The Touch-induced action potential in Chara: Inquiry into the ionic basis and the mechanoreceptor. Functional Plant Biol. 20(5):471–488. doi:10.1071/PP9930471.
   Google Scholar
• Barry WH. 1968. Coupling of excitation and cessation of cyclosis in Nitella: role of divalentcations. J Cell Physiol. 72(3):153–159. doi:10.1002/jcp.1040720303.
   PubMed Web of Science ®Google Scholar
• Wayne R, Staves M. 1991. The density of the cell sap and endoplasm of Nitellopsis and Chara. Plant Cell Phys. 32:1137–1144.
   PubMed Web of Science ®Google Scholar
• Wallis S. 2013. Binomial confidence intervals and contingency tests: Mathematical fundamentals and the evaluation of alternative methods. J Quant Linguistics. 20(3):178–208. doi:10.1080/09296174.2013.799918.
   Web of Science ®Google Scholar
• Shimmen T, Yokota E. 1994. Physiological and biochemical aspects of cytoplasmic streaming. Int Rev Cytol. 155:97–139.
   Google Scholar
• Shimmen T. 1996. Studies on mechano-perception in Characean Cells: Development of a monitoring apparatus. Plant Cell Physiol. 37(5):591–597. doi:10.1093/oxfordjournals.pcp.a028986.
   Web of Science ®Google Scholar
• Shimmen T. 2001. Involvement of receptor potentials and action potentials in mechano-perception in plants. Functional Plant Biol. 28(7):567–576. doi:10.1071/PP01038.
   Google Scholar
• Kikuyama M, Shimada K, Hiramoto Y. 1993. Cessation of cytoplasmic streaming follows an increase of cytoplasmic Ca2+ during action potential in Nitella. Protoplasma. 174(3–4):142–146. doi:10.1007/BF01379046.
   Web of Science ®Google Scholar
• Shimmen T, Kikuyama M, Tazawa M. 1995. Studies on cessation of cytoplasmic streaming under K+-induced depolarization in Nitella axilliformis. J Plant Res. 108(4):457–462. doi:10.1007/BF02344234.
   Google Scholar
• Wayne R. 1993. Excitability in plant cells. Am Sci. 81:140–151.
   Web of Science ®Google Scholar
• Wayne R. 1994. The excitability of plant cells: With a special emphasis on characean internodal cells. Bot Rev. 60(3):265–367. doi:10.1007/BF02960261.
   PubMed Web of Science ®Google Scholar
• Kamitsubo E, Kikuyama M. 1992. Immobilization of endoplasm flowing contiguous to the actin cables upon electrical stimulus in Nitella internodes. Protoplasma. 168(1–2):82–86. doi:10.1007/BF01332653.
   Web of Science ®Google Scholar
• Johnson B, Wyttenbach R, Wayne R, Hoy R. 2002. Action potentials in a giant algal cell: a comparative approach to mechanisms and evolution of excitability. J Undergrad Neurosci Educ. 1(1):A23–A27. PMID: 23493389; PMCID: PMC3592585.
   PubMedGoogle Scholar
• Wayne R, Staves M, Leopold AC. 1990. Gravity-dependent polarity of cytoplasmic streaming in Nitellopsis. Protoplasma. 155(1–3):43–57. doi:10.1007/BF01322614.
   PubMed Web of Science ®Google Scholar
• Whitaker AM, Jones CS. 1965. Report of 1500 chloroform anesthetics administered with a precision vaporizer. Anesth Analg. 44(1):60–65. doi:10.1213/00000539-196501000-00016.
   PubMed Web of Science ®Google Scholar
• Kelz MB, Mashour GA. 2019. The biology of general anesthesia from Paramecium to primate. Curr Biol. 29(22):R1199–R1210. doi:10.1016/j.cub.2019.09.071.
   PubMed Web of Science ®Google Scholar
• Sonner JM. 2008. A hypothesis on the origin and evolution of the response to inhaled anesthetics. Anesth Analg. 107(3):849–854. doi:10.1213/ane.0b013e31817ee684.
   PubMed Web of Science ®Google Scholar
• Kühne W. 1864. Untersuchungen über das Protoplasma und die Contractilität. Leipzig: Engelmann; p. 158.
   Google Scholar
• Osterhout W, Harris E. 1928. Protoplasmic asymmetry in Nitella as shown by bioelectric measurements. J Gen Physiol. 11:391–406. doi:10.1085/jgp.11.4.391. PMID: 19872407; PMCID: PMC2140986.
   PubMedGoogle Scholar
• Nichols S. 1930. The effect of chloroform upon the rotation in the internodes of Nitella Bull. Torrey Bot Club. 57(3):153–162. doi:10.2307/2480632.
   Google Scholar
• Grémiaux A, Yokawa K, Mancuso S, Baluška F. 2014. Plant anesthesia supports similarities between animals and plants. Plant Signal Behav. 9(1):1–4. doi:10.4161/psb.27886.
   Google Scholar
• Clar D, Patel S, Richards J. 2023. Anesthetic Gases. In: StatPearls [Internet]. US: StatPearls Publishing; [accessed 2024 Jan]. https://www.ncbi.nlm.nih.gov/books/NBK537013/.
   Google Scholar
• Herold KF, Andersen OS, Hemmings HC Jr. 2017. Divergent effects of anesthetics on lipid bilayer properties and sodium channel function. Eur Biophys J. Oct;46(7):617–626. doi:10.1007/s00249-017-1239-1. Epub 2017 Jul 10. PMID: 28695248; PMCID: PMC5693657.
   PubMed Web of Science ®Google Scholar
• Yokawa K, Kagenishi T, Baluška F. 2019. Anesthetics, Anesthesia, and Plants. Trends Plant Sci. 24(1):12–14. doi:10.1016/j.tplants.2018.10.006.
   PubMed Web of Science ®Google Scholar
• Graesbøll K, Sasse-Middelhoff H, Heimburg T. 2014. The thermodynamics of general and local anesthesia. Biophys J. 106(10):2143–2156. doi:10.1016/j.bpj.2014.04.014. PMID: 24853743; PMCID: PMC4064590.
   PubMed Web of Science ®Google Scholar
• Deng J, Lei C, Chen Y, Fang Z, Yang Q, Zhang H, Cai M, Shi L, Dong H, Xiong L. 2014. Neuroprotective gases–fantasy or reality for clinical use? Prog Neurobiol. 115:210–245. doi:10.1016/j.pneurobio.2014.01.001.
   PubMed Web of Science ®Google Scholar
• Andersen OS, Koeppe RE 2nd. 2007. Bilayer thickness and membrane protein function: an energetic perspective. Annu Rev Biophys Biomol Struct. 36(1):107–130. doi:10.1146/annurev.biophys.36.040306.132643.
   PubMedGoogle Scholar