Abstract
It has always been customary to remove the meninges prior to examining the brain. Deprived of meninges, the brain surface appears smooth and without any apparent vascularity, a well-known fact to anyone interested in studying it. An apparently avascular surface is also applicable to the cerebellum, medulla, and spinal cord deprived of meninges (Fig. 1). This is intriguing considering that the first 2.5 mm below the brain surface has one richer cellular and functionally active region of the human body, namely, the cortex gray matter where most neurons reside. Brain oxygen consumption represents roughly 20% of that consumed by the entire body although it only represents a small fraction of its volume (Hossmann 1994). Therefore, the cortex gray matter, where most neurons reside, must be richly vascularized, a fact that conflicts with its apparently avascular surface.
By removing the meninges, the vascular elements connecting the meninges and brain are severed leaving its surface apparently avascular (Fig. 1). Recent studies have demonstrated that these connecting vessels originate in the pial anastomotic capillary plexus, an important vascular compartment of the meninges that has remained essentially ignored (Marín-Padilla 2012). The pial capillaries establish a short-linked anastomotic plexus that covers the cortex’ expanding surface. The capillary size ranges from 3 to 7 μm and is, therefore, invisible to unaided observation. The meninges removal inevitably will carry the pial capillaries that will be lost when it is discarded. Perhaps, the invisibility of pial capillaries as well as the customary meninges castoff could explain why both the connecting capillaries and the pial anastomotic capillary plexus have been seldom recognized. The smooth and apparently avascular surface of the mammalian brain, deprived of meninges, has become a well-known and undisputed fact (Fig. 1).
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Dorsal, ventral, and lateral views of the human brain deprived of the meninges, from a 30-week-old fetus, showing its smooth and apparently avascular surface. The meningeal removal carried out prior to any brain examination leaves its surface apparently avascular. By removing the meninges, the pial capillaries connecting meninges to the brain are all severed. An apparently avascular surface also applies to the cerebellum, pons, and spinal cord deprived of meninges. A good magnifying glass demonstrates the presence of small and equidistant orifices with a severed vessel inside each one, throughout the cortex entire surface. The vessels connecting the meninges and the brain originate in the pial anastomotic capillary plexus, an important meningeal vascular compartment often ignored. The pial capillaries are invisible to unaided (naked eye) observation and are invariably removed with the meninges
The simple inspection of the cortex surface (deprived of meninges) with a good magnifying glass (or dissecting microscope) solves the dilemma (Marín-Padilla 2012). Throughout its entire surface, there are small openings with a severed small blood vessel on each one. The orifices represent the Virchow-Robin compartments, clearly distinguishable from the severed blood vessel inside them. Both the orifices and their inside vessels are invisible to unaided (naked eye) observation. Anyone with a good magnifying glass could corroborate these observations, which are also applicable to any mammalian brain deprived of meninges.
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References
Andres KH (1976a) Überdie Feinstrukture der Arachnoidea und Dura mater von Mammalia. Zeitschrift Zellsforschung Microskoscopic Anat 82:272–295
Andres KH (1976b) Zur Feinstruktur der Arachnoidal zotten bei Mammalia. Zeitschrift Zellsforchung Mikroskoscopic Anat 82:92–109
Bär T, Wolff JR (1972) The formation of capillary basement membranes during internal vascularization of the rat’s cerebral cortex. Zellsforchung Microskopic Anat 133:231–248
Blinkov SM, Glezer II (1968) The human brain in figures and tables. Plenum Press/Basic Books, New York
Buitrago-Delgado E, Nordin K, Rao A, Geary L, LaBonne C (2015) Shared regulatory programs suggest retention of blastula-stage potential in neural crest cells. Science 384:1332–1335
Cajal S y R (1911) Histologie du Systéme Nerveux de L’homme et des Vertebrés. Maloine, Paris. (Reprinted by CSIC, Madrid 1952)
Casley-Smith AB, Földi-Börcsök E, Földi M (1976) The prelymphatic pathways of the brain as revealed by cervical lymphatic obstruction and the passage of particles. Br J Exp Pathol 57:179–188
Dorovini-Zis K (2015) In: Dorovini-Zis K (ed) The blood-brain barrier in health and disease, vol 1, Morphology, biology, and immune function. CRC Press/Taylor & Francis Group, Boca Raton/New York
Duvernoy HM, Delon S, Vannson JL (1981) Cortical blood vessels of the human brain. Brain Res Bull 7:519–579
Gamble HJ (1975) Preliminary observations on the vascularization of the human embryonic brain. J Anat 118:212–227
Golgi C (1873) Sulla sostanza grigia del cervello. Gaz Med Ital Lombardia 6:244–246
Hamilton WJ, Boyd JD, Mossman HW (1972) Human embryology. Heffer, Cambridge, UK
Hauw JJ, Berger JR, Escourolle R (1975) Electron microscopic study of the develo** capillaries of the human brain. Acta Neuropathol 31:229–242
Hossmann KA (1994) Viability thresholds and the penumbra of focal ischemia. Ann Neurol 36:557–565
Jeffrey JI, Wang M, Liao J, Plogg BA, Peng W, Gundersen GA, Benveniste H, Vates GE, Deane R, Golman SA, Nagelhus BA, Nedergard M (2012) Paravascular pathway facilitates CSF flow through the brain parenchyma and the clearance of interstitial solutes, including amyloid. Sci Transl Med 4:1–11
Jones EG (1970) On the mode of entry of blood vessels into the cerebral cortex. J Anat 106:507–520
Klosouskii BN (1963) Blood circulation on the brain (trans: from Russian by the Israel Program for Scientific Translations). Jerusalem
Krahn V (1982) The pia mater at the site of entry of blood vessels into the central nervous system. Anat Embryol 164:257–263
Krisch B, Leonhardt H, Oksche A (1982) The meningeal compartment of the median eminence and cortex: a comparative analysis in the rat. Cell Tissue Res 228:597–640
Krisch B, Leonhardt H, Oksche A (1983) Compartment and perivascular arrangement of the meninges covering the cerebral cortex of the rat. Cell Tissue Res 338:459–474
Larroche J-C (1977) Developmental pathology of the neonate. Elsevier North Holland Biomedical Press, Amsterdam
Larsen WJ (1997) Human embryology. Churchill Livingston, New York
Mall EP (1904) On the development of blood vessels of the brain in human embryos. Am J Anat 4:1–18
Marín-Padilla M (1988) Embryonic vascularization of the mammalian cerebral cortex. In: Peters A, Jones EC (eds) Cerebral cortex, vol 7. Plenum Press, New York
Marín-Padilla M (1995) Prenatal development of fibrous (white matter), protoplasmic (gray matter), and layer I astrocytes in the human cerebral cortex: a Golgi study. J Comp Neurol 358:1–119
Marín-Padilla M (1996) Developmental neuropathology and impact of perinatal brain damage. I. Hemorrhagic lesions of the neocortex. J Neuropath Exp Neurol 55:746–762
Marín-Padilla M (1997) Developmental neuropathology and impact of perinatal brain damage. II White matter lesions of the neocortex. J Neuropath Exp Neurol 56:219–235
Marín-Padilla M (1999) Developmental neuropathology and impact of perinatal brain damage. III Gray matter lesions of the neocortex. J Neuropath Exp Neurol 58:407–429
Marín-Padilla M (2000) Perinatal brain damage, cortical reorganization (acquired cortical dysplasia) and epilepsy. In: Williamson P, Siegel AM, Roberts D, Vijaw VM, Gazzaniga M (eds) Neocortical epilepsies. Lippincott Williams and Wilkins, Philadelphia
Marín-Padilla M (2011) The human brain: prenatal development and structure. Springer, Heidelberg
Marín-Padilla M (2012) The human brain intracerebral microvascular system: development and structure. Front Neuroanat 6:38. https://doi.org/10.3389/fnana00038
Marín-Padilla M (2014) The mammalian neocortex new pyramidal neuron: a new conception. Front Neuroanat 7:51. https://doi.org/10.3389/fnana.2013
Marín-Padilla M, Knopman D (2011) Developmental aspects of the intracerebral microvasculature and perivascular spaces: insights into the brain response to late-life diseases. J Neuropath Exp Neurol 70:1–10
Marín-Padilla M, Parisi JE, Amstrong DL, Kaplan JA (2002) Shaken infant syndrome: developmental neuropathology, progressive cortical dysplasia and epilepsy. Acta Neuropathol 103:321–332
Marín-Padilla, M (2015) The Human Cerebral Cortex Microvascular System: Development and Composition of the Meningeal and Intracerebral Extrinsic and Intrinsic (Blood-Brain-Barrier) Compartments. In: Katerina Dorovini-Zis (Ed), The Blood Brain Barrier, In Health and Disease. CRC Press. Taylor & Francis Group. New York. pp. 51–69.
Mountcastle VB (1978) An organizing principle for cerebral function: the unit module and the distributed system. In: Adelman GM, Mountcastle VB (eds) The mindful brain. MIT Press, Cambridge, MA
Nabeshina S, Reese RS, Landis MD (1975) Junction of meninges and marginal glia. J Comp Neurol 164:127–170
O’Rahilly R, Müller F (1999) The embryonic human brain. An atlas of developmental stages. Willey-Liss Publications, New York
Padget DH (1948) The development of the cranial arteries in the human embryo. Contrib Embryol Carnegie Inst 32:207–261
Padget DH (1957) The development of the cranial venous system in man: from the point of view of comparative anatomy. Contrib Embryol Carnegie Inst 34:79–140
Pape EK, Wigglesworth JS (1979) Hemorrhages, ischemia and the perinatal brain. Spastic International Medical Publications, London
Pile-Spelman J, Mckusic KA, Strauss HW, Coony J, Taveras JM (1984) Experimental in vivo imaging of the cranial perineural lymphatic pathway. Am J Neuroradiol 5:539–545
Puelles L, Malagon F, Martinez de la Torre M (1976) Study of capillary buds during in the interior of the embryonal central nervous system by the method of Golgi. Anales del Desarrollo 20:89–91
Stretter GL (1918) The developmental alterations in the vascular system of the brain in the human embryo. Contrib Embryol Carnegie Inst 8:5–38
Strong LH (1964) The early embryonic pattern on internal vascularization of the mammalian cerebral cortex. J Comp Neurol 123:121–138
Ussui Y, Westenskow PD, Kurihara T, Aguilar E, Sakimoto S, Paris LP, Wittgrove C, Feitelberg D, Friedlander MS, Moreno SK, Dorrell MI, Friedlander M (2015) Neurovascular crosstalk between interneurons and capillaries is required for vision. JCI 125:2335–2346
Wolff JR, Goetz C, Bär T, Guldner EB (1975) Common morphogenetic aspects of various organotypic microvascular patterns. Microvasc Res 10:373–395
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Marín-Padilla, M. (2022). Cerebral Microvessels. In: Pfaff, D.W., Volkow, N.D., Rubenstein, J.L. (eds) Neuroscience in the 21st Century. Springer, Cham. https://doi.org/10.1007/978-3-030-88832-9_137
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