Relationship between Temperature in the Deep Layers of the Somatosensory Cortex and Blood Flow Velocity in the Brain of Anesthetized Mice
- Authors: Romshin A.M1, Osypov A.A2,3, Krohaleva V.K1,2, Zhuravlev S.G1, Egorova O.N1, Vlasov I.I1, Popova I.Y.1,2
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Affiliations:
- Prokhorov Institute of General Physics, Russian Academy of Sciences
- Institute of Theoretical and Experimental Biophysics, Russian Academy of Sciences
- Institute of Higher Nervous Activity and Neurophysiology, Russian Academy of Sciences
- Issue: Vol 69, No 2 (2024)
- Pages: 356-363
- Section: Articles
- URL: https://journals.rcsi.science/0006-3029/article/view/257586
- DOI: https://doi.org/10.31857/S0006302924020189
- EDN: https://elibrary.ru/OTNMKM
- ID: 257586
Cite item
Abstract
Keywords
About the authors
A. M Romshin
Prokhorov Institute of General Physics, Russian Academy of SciencesMoscow, Russia
A. A Osypov
Institute of Theoretical and Experimental Biophysics, Russian Academy of Sciences; Institute of Higher Nervous Activity and Neurophysiology, Russian Academy of SciencesMoscow, Russia; Moscow, Russia
V. K Krohaleva
Prokhorov Institute of General Physics, Russian Academy of Sciences; Institute of Theoretical and Experimental Biophysics, Russian Academy of SciencesMoscow, Russia; Moscow, Russia
S. G Zhuravlev
Prokhorov Institute of General Physics, Russian Academy of SciencesMoscow, Russia
O. N Egorova
Prokhorov Institute of General Physics, Russian Academy of SciencesMoscow, Russia
I. I Vlasov
Prokhorov Institute of General Physics, Russian Academy of SciencesMoscow, Russia
I. Yu Popova
Prokhorov Institute of General Physics, Russian Academy of Sciences; Institute of Theoretical and Experimental Biophysics, Russian Academy of Sciences
Email: I-Yu-Popova@yandex.ru
Moscow, Russia; Moscow, Russia
References
- Kiyatkin E. A. Brain temperature and its role in physiology and pathophysiology: Lessons from 20 years of thermorecording. Temperature (Austin), 6 (4), 271–333 (2019). doi: 10.1080/23328940.2019.1691896
- Sung D., Risk B. B., Wang K. J., Allen J. W., and Fleischer C. C. Resting-state brain temperature: dynamic fluctuations in brain temperature and the brainbody temperature gradient. J. Magn. Reson. Imaging, 57 (4),1222–1228 (2023). doi: 10.1002/jmri.28376
- Minamisawa H., Nordstrom C. H., Smith M. L., and Siesjö B. K. The influence of mild body and brain hypothermia on ischemic brain damage. J. Cereb. Blood Flow Metab., 10 (3), 365–374 (1990). doi: 10.1038/jcbfm.1990.66
- Blatteis C. M. The onset of fever: new insights into its mechanism. Prog. Brain Res., 162, 3–14 (2007). doi: 10.1016/S0079-6123(06)62001-3
- Moltz H. Fever: causes and consequences. Neurosci. Biobehav. Rev., 17 (3), 237–369 (1993). doi: 10.1016/s0149-7634(05)80009-0
- Siesjö B. K. Brain energy metabolism (John Wiley & Sons, New York, 1978).
- Falk D. Brain evolution in Homo: The “radiator” theory. Behav. Brain Sci., 13 (2), 333–344 (1990). DOI: https://doi.org/10.1017/S0140525X00078973
- Dehkharghani S. and Qiu D. MR thermometry in cerebrovascular disease: physiologic basis, hemodynamic dependence, and a new frontier in stroke imaging. AJNR Am. J. Neuroradiol., 41 (4), 555–565 (2020). doi: 10.3174/ajnr.A6455
- Zhu M., Ackerman J. J., and Yablonskiy D. A. Body and brain temperature coupling: the critical role of cerebral blood flow. J. Comp. Physiol. B, 179 (6), 701–710 (2009). doi: 10.1007/s00360-009-0352-6
- Nybo L., Secher N. H., and Nielsen B. Inadequate heat release from the human brain during prolonged exercise with hyperthermia. J. Physiol. 545 (2), 697–704 (2002). doi: 10.1113/jphysiol.2002.030023
- Yablonskiy D. A., Ackerman J. J., and Raichle M. E. Coupling between changes in human brain temperature and oxidative metabolism during prolonged visual stimulation. Proc. Natl. Acad. Sci. USA, 97 (13), 7603–7608 (2000). doi: 10.1073/pnas.97.13.7603
- McIlvoy L. Comparison of brain temperature to core temperature: A review of the literature. J. Neurosci. Nurs., 36 (1), 23–31 (2004). doi: 10.1097/01376517-200402000-00004
- Williams L. R. and Leggett R. W. Reference values for resting blood flow to organs of man. Clin. Phys. Physiol. Meas., 10 (3), 187–217 (1989). doi: 10.1088/0143-0815/10/3/001
- Baker M. A. and Chapman L. W. Rapid brain cooling in exercising dogs. Science, 195 (4280), 781–783 (1977). doi: 10.1126/science.836587
- Jessen C. Selective brain cooling in mammals and birds. Jpn. J. Physiol., 51 (3), 291–301 (2001). doi: 10.2170/jjphysiol.51.291
- Drew P. J. Neurovascular coupling: motive unknown. Trends Neurosci., 45 (11), 809–819. (2022). doi: 10.1016/j.tins.2022.08.004
- Gordon G. R., Choi H. B., Rungta R. L., EllisDavies G. C., and MacVicar B. A. Brain metabolism dictates the polarity of astrocyte control over arterioles. Nature, 456 (7223), 745–749 (2008). doi: 10.1038/nature07525
- Paxinos G., Franklin K. B. J., S. D.: Academic Press (2001). Paxinos G. and Franklin K. B. J. The Mouse Brain in Stereotaxic Coordinates. 2nd Edition (Acad. Press, San Diego, 2001).
- Winship I. R. Laser speckle contrast imaging to measure changes in cerebral blood flow. Methods Mol. Biol. (Clifton, NJ), 135, 223–235 (2014). doi: 10.1007/978-1-4939-0320-7_19
- Romshin A. M., Zeeb V., Martyanov, A. K., Kudryavtsev O. S., Sedov V. S., Ralchenko V. G., Sinogeykin A. G., and Vlasov I. I. A new approach to precise mapping of local temperature fields in submicrometer aqueous volumes. Sci Rep., 11, 14228 (2021). doi: 10.1038/s41598-021-93374-7
- Malkov A., Ivanov A. I., Popova I., Mukhtarov M., Gubkina O., Waseem T., Bregestovski P., and Zilberter Y. Reactive oxygen species initiate a metabolic collapse in hippocampal slices: potential trigger of cortical spreading depression. J. Cereb. Blood Flow Metab., 34 (9), 1540–1549 (2014). doi: 10.1038/jcbfm.2014.121.
- Fedotov I. V., Solotenkov M. A., Pochechuev M. S., Ivashkina O. I., Kilin S. Ya., Anokhin K. V., and Zheltikov A. M. All-optical brain thermometry in freely moving animals. ACS Photonics, 7, 3353–3360 (2020). doi: 10.1021/acsphotonics.0c00706
- Petrini G., Tomagra G., Bernardi E., Moreva E., Traina P., Marcantoni A., Picollo F., Kvaková K., Cígler P., Degiovanni I. P., Carabelli V., and Genovese M. Nanodiamond–quantum sensors reveal temperature variation associated to hippocampal neurons firing. Adv. Sci., 9 (28), e2202014 (2022). doi: 10.1002/advs.202202014
- Marín J. and Rivilla F. Nerve endings and pharmacological receptors in cerebral vessels. Gen. Pharmacol., 13 (5), 361–368 (1982). doi: 10.1016/0306-3623(82)90100-8
- Toussay X., Basu K., Lacoste B., and Hamel E. Locus coeruleus stimulation recruits a broad cortical neuronal network and increases cortical perfusion. J. Neurosci., 33 (8), 3390–3401 (2013). doi: 10.1523/JNEUROSCI.3346-12.2013X
- Abdul-Rahman A., Dahlgren N., Johansson B. B., and Siesjö B. K. Increase in local cerebral blood flow induced by circulating adrenaline: involvement of bloodbrain barrier dysfunction. Acta Physiol Scand., 107 (3), 227–332 (1979). doi: 10.1111/j.1748-1716.1979.tb06467.x
- N. Dahlgren, I. Rosen, T. Sakabe, and Siesjö B. K. Cerebral functional, metabolic and circulatory effects of intravenous infusion of adrenaline in the rat. Brain Res., 184 (1), 143–152 (1980). doi: 10.1016/0006-8993(80)90593-4
- Sokrab T. E. and Johansson B. B. Regional cerebral blood flow in acute hypertension induced by adrenaline, noradrenaline and phenylephrine in the conscious rat. Acta Physiol. Scand., 137 (1), 101–106 (1989). doi: 10.1111/j.1748-1716.1989.tb08725.x
- Borchardt R.T. Catechol o-methyltransferase. Methods Enzymol., 77, 267–272 (1981). doi: 10.1016/s0076-6879(81)77036-8
- Del Franco A. P. and Newman E. A. Astrocyte β-adrenergic receptor activity regulates NMDA receptor signaling of medial prefrontal cortex pyramidal neurons. J. Neurosci., 44 (2), e0990232023 (2023). DOI: 10.1523/ JNEUROSCI.0990-23.2023
- Reyner-Parra D., Bonet C., Seara T. M., and Huguet G. Traveling waves in a model for cortical spreading depolarization with slow–fast dynamics. Chaos, 33 (8), 083154 (2023). doi: 10.1063/5.0160509
- Sawant-Pokam P. M., Suryavanshi P., Mendez J. M., Dudek F. E., and Brennan K. C. Mechanisms of neuronal silencing after cortical spreading depression. Cereb. Cortex., 27 (2), 1311–1325 (2017). doi: 10.1093/cercor/bhv328P
- Kaufmann D., Theriot J. J., Zyuzin J., Service C. A., Chang J. C., Tang Y. T., Bogdanov V. B., Multon S., Schoenen J., Ju Y. S., and Brennan K.C. Heterogeneous incidence and propagation of spreading depolarizations. J. Cereb. Blood Flow Metab., 37 (5), 1748–1762 (2017). doi: 10.1177/0271678X16659496D
- Xu S., Chang J. C., Chow C. C., Brennan K. C., and Huang H. A mathematical model for persistent postCSD vasoconstriction. PLoS Comput. Biol., 16 (7), e1007996 (2020). doi: 10.1371/journal.pcbi.1007996S
- Busija D. W., Bari F., Domoki F., Horiguchi T., and Shimizu K. Mechanisms involved in the cerebrovascular dilator effects of cortical spreading depression. Prog. Neurobiol., 86 (4), 379–395 (2008). doi: 10.1016/j.pneurobio.2008.09.008D
- Hsieh B. Y., Kao Y.-C., Zhou J. N., Lin Yi.-P., Mei Yu.-Y., Chu S.-Yu., and Wu D.-Ch. Vascular responses of penetrating vessels during cortical spreading depolarization with ultrasound dynamic ultrafast Doppler imaging. Front. Neurosci., 16, 1015843 (2022). doi: 10.3389/fnins.2022.1015843
- Wang Y., Wang Y., Yue G., and Zhao Y. Energy metabolism disturbance in migraine: From a mitochondrial point of view. Front. Physiol., 14, 1133528 (2023). doi: 10.3389/fphys.2023.1133528Y
- Chrétien D., Bénit P., Ha H. H., Keipert S., ElKhoury R., Chang Y. T., Jastroch M., Jacobs H. T., Rustin P., and Rak M. Mitochondria are physiologically maintained at close to 50°C. PLoS Biol. 16 (1), e2003992 (2018). doi: 10.1371/journal.pbio.2003992D
- Romshin A. M., Osypov A. A., Popova I. Y., Zeeb V. E., Sinogeykin A. G., and Vlasov I. I. Heat release by isolated mouse brain mitochondria detected with diamond thermometer. Nanomaterials (Basel), 13 (1), 98 (2023). doi: 10.3390/nano13010098