A COMPARATIVE STUDY OF THE LIPIDS OF THE VERTEBRATE CENTRAL NERVOUS SYSTEM

Similar documents
A COMPARATIVE STUDY OF THE LIPIDS OF THE VERTEBRATE CENTRAL NERVOUS SYSTEM

glands are reported to have no antidiuretic action) produce a principle gland of some lower vertebrates (teleost fishes, amphibians, reptiles), has

Classification of Lipids

THE IODINE CONTENT OF THE THYROID OF THE FOWL WITH REFERENCE TO AGE AND SEX

Classification, functions and structure

II- Compound Lipids. 1- Phospholipids

Lecture 3 6/28/10. Membrane Lipids. Importance of Membranes. Categories of Lipids. Lipids: Chapter 20 Sections 4-7. ! Membranes are important in

Lipid Chemistry. Presented By. Ayman Elsamanoudy Salwa Abo El-khair

THE INTIMA of the arterial system, a

(From the Physiological Laboratory, University College.)

Test Bank for Lehninger Principles of Biochemistry 5th Edition by Nelson

Biological role of lipids

OF NORMAL AND SCORBUTIC GUINEA-PIGS

Department of Anatomy, Glasgow University

Carboxylic acids is а compound whose characteristic functional group is the carboxyl group -COOH, example:

THE WATER-BALANCE PRINCIPLE OF CRUSTACEAN EYE-STALK EXTRACTS

THE ACTION OF DRUGS, ESPECIALLY ACETYL- CHOLINE, ON THE ANNELID BODY WALL {LUMBRICUS, ARENICOLA)

PHOSPHOLIPIDS METABOLISM. BY Dr. Walid Said Zaki Dr. Marwa Ali LECTURER OF BIOCHEMISTRY AND MOLECULAR BIOLOGY

METABOLISM OF ACYLGLYCEROLS AND SPHINGOLIPDS. Ben S. Ashok MSc.,FAGE.,PhD., Dept. of Biochemistry

Dr. Nafith Abu Tarboush


Chem 431A-L24-F 07 admin: Last time: We finished Chapt 7, started Chapt 10 FA s and TG s FA=fatty acid, TG=triglycerides or triacylglycerols

Chromatography of sphingolipids of human brain*

LIPIDS II: TRIACYLGLYCEROLS:

Phospholipids Metabolism

4) Modification of Development by Sensory Experience (Nurture)

Chapter 20 Lipids. Organic and Biochem

INTRODUCTION. IN a previous paper(l) we have been able to show that adrenaline may

Nervous Systems: Diversity & Functional Organization

Lipids and Membranes

Consequently, lipoprotein fractions have been analyzed

LOCALIZATION OF MONOAMINE OXIDASE IN MAMMALIAN

CHAPTER 8 COMPARATIVE ANALYSIS OF ASSOCIATIVE LEARNING

[Gaskell, 1880] produced vaso-dilatation of muscle, and in a concentration

Chapter 8. Functions of Lipids. Structural Nature of Lipids. BCH 4053 Spring 2001 Chapter 8 Lecture Notes. Slide 1. Slide 2.

The Effect of Some Marine Oils and Squalene on the Plasma Cholesterol in Chicks

Neurogenic and Myogenic hearts

THE UPTAKE OF PHOSPHATE BY EXCISED MYCORRHIZAL ROOTS OF THE BEECH

A comparison of the sensitivities of innervated and denervated rat vasa deferentia to agonist drugs

TEST BANK FOR LEHNINGER PRINCIPLES OF BIOCHEMISTRY 6TH EDITION BY NELSON

triplelayered unit for the plasma cell membrane component; two such Model parameters are assigned to three varieties of peripheral nerve

Increased Utilization of an Amino Acid and Cellular Proliferation Demonstrated Auto- radiographically in the Optic Pathways of Pigeons

Lipids and Biological Membranes

THE ABSORPTION OF VOLATILE FATTY ACIDS FROM THE RUMEN

Lipids. Lipids. Jiří Jonák and Lenka Fialová Institute of Medical Biochemistry, 1st Medical Faculty of the Charles University, Prague

UNIT ACTIVITY IN THE MEDULLA OBLONGATA OF FISHES

BIOLOGY 183 MARINE BIOLOGY PIMA COMMUNITY COLLEGE, DOWNTOWN CAMPUS WORKSHEETS FOR UNIT 7 UNIT 7 LEARNING OBJECTIVES UNIT 7 ACTIVITIES

Adult Nervous System

THE EFFECTS OF CHOLESTEROL DOSAGE, CORTISONE, AND DCA ON TOTAL SERUM CHOLESTEROL, LIPOPROTEINS, AND ATHEROSCLEROSIS IN THE RABBIT

ENHANCEMENT OF THE GRANULATION OF ADRFNERGIC STORAGE VESICLES IN DRUG-FREE SOLUTION

COMMON FORMATIVE ASSESSMENT PLANNING TEMPLATE --FIRST DRAFT--

possibility of a secretion of adrenaline from the suprarenal glands resulting

susceptibility of either the axons in the dorsal and ventral roots, or the intramedullary

ANSC (NUTR) 618 LIPIDS & LIPID METABOLISM Membrane Lipids and Sphingolipidsd

NEURONS Chapter Neurons: specialized cells of the nervous system 2. Nerves: bundles of neuron axons 3. Nervous systems

Lipid changes in Duchenne muscular dystrophy

Comparing Vertebrates: Fetal Pig and Bullfrog Honors Integrated Science 4

Opinion on the safety assessment of phospholipds obtained from egg yolk as food produced using a new process

Scheminzky's phenomenon was attempted by studying the actions of galvanic. Scheminzky (see Scheminzky, 1940, 1947, and the papers quoted therein) has

Chapter 28: Lipids In a slightly different order than in your textbook Fatty Acids

MEMBRANE LIPIDS I and II: GLYCEROPHOSPHOLIPIDS AND SPHINGOLIPIDS

Phylogenesis of the nervous system.

OF FATTY LIVERS. XLII. PROTEIN AND THE DIETARY PRODUCTION. On a number of occasions however use of this diet has failed to produce in our

Brain Comparisons of Animals from the Five Vertebrate Classes

Lipids. Lipids: a Diverse group of chemicals. Storage Lipids: derivatives of fatty acids. 11/21/10

GUTS Lecture Syllabus for Lipid Structure and Nomenclature

Chem 464 Biochemistry

The effect of phosphatidyl choline on the degradation of phosphatidyl ethanolamine by the phospholipase of post-heparin plasma or snake venom

STANDARD OPERATING PROCEDURE #403 GUIDELINES FOR BLOOD COLLECTION VOLUMES AND FREQUENCY

The Nervous System. Nerves, nerves everywhere!

(Received 27 November 1953)

Classes #5-6: Specializations in CNS evolution

12 Anatomy and Physiology of Peripheral Nerves

UNIVERSITY OF CAMBRIDGE INTERNATIONAL EXAMINATIONS International General Certificate of Secondary Education

CIRCULATION IN CONGENITAL HEART DISEASE*

ISOSMOTIC REGULATION IN VARIOUS TISSUES OF THE DIAMONDBACK TERRAPIN MALACLEMYS CENTRATA CENTRATA (LATREILLE)*

SERUM VITAMIN A AND TOTAL PLASMA LIPID CONCENTRATIONS

Fertilization. Bởi: OpenStaxCollege

Introduction and aims of the study

Disappearance of small vesicles from adrenergic nerve endings in the rat vas deferens caused by red back spider venom

Yasser Moh. Aneis, PhD, MSc., PT. Lecturer of Physical Therapy Basic Sciences Department

THE INFLUENCE OF INSULIN ON GLYCOGEN DISTRIBU- TION IN MARINE FISHES

Biochemistry. Classification of Lipids METABOLISM OF LIPIDS. Principal Investigator

CELL MEMBRANES (MAS)

[66] THE PHYSIOLOGY OF SEA-URCHIN SPERMATOZOA

INFLUENCE OF TEMPERATURE ON THE AMYLASES OF COLD- AND WARM-BLOODED ANIMALS

suggesting that the release of noradrenaline from sympathetic fibres was dependent on the concentration of Ca2+ outside the fibre.

THE EFFECT OF ROENTGEN RADIATION ON SPINAL GANGLIA OF ALBINO RATS

Tyrosinase Activity in the Pigmented Cells of the Nucleus Substantiae Nigrae. I. Monophenolase and Diphenolase Activity. By C. D.

J. Physiol. (I957) I35, (Received 20 July 1956) The interpretation ofthe experimental results ofthe preceding paper (Matthews

Teacher Key. Big Idea Different types of neurons compose the nervous tissue that forms the communication system within the body.

BIOLOGY (SPECIFICATION A) Unit 6 Physiology and the Environment

MAST-CELLS are present in the digestive tract of all classes of vertebrates

CHAPTER 26. Circulation and Gas Exchange

THE ACTION OF NICOTINE ON THE CILIARY GANGLION

however, reduced after parasympathetic denervation [Nordenfelt et al., 1960]. opposite to those caused by parasympathetic denervation.

Manuscript Version Sage holds the Copyright. Introduction. Seemingly, no two investigators agree on what intelligence means or includes, but

below. METHODS GALACTOSE ABSORPTION FROM THE SURVIVING SMALL INTESTINE OF THE RAT

HASPI Medical Anatomy & Physiology 11a Lab Activity

Ex : Butter contain large proportion of short chains of fatty acids, so it has high saponification number while margarine with more long fatty acids,

Transcription:

[ 2O3 ] A COMPARATIVE STUDY OF THE LIPIDS OF THE VERTEBRATE CENTRAL NERVOUS SYSTEM II. SPINAL CORD BY J. D. MCCOLL AND R. J. ROSSITER Department of Biochemistry, University of Western Ontario, London, Canada {Received 13 August 1951) (With One Text-figure) INTRODUCTION In the preceding paper McColl & Rossiter (1952) reported the concentration of water, cerebroside, total cholesterol, total phospholipin, sphingomyelin, lecithin, kephalin and myelin lipid in the brains of a representative series of vertebrates. This paper describes the distribution of these substances in the spinal cords of the same series of vertebrates. METHODS The species studied and the analytical methods were the same as those described in the previous paper (McColl & Rossiter, 1952). Samples of spinal cord were removed from each specimen as soon as possible after death. The sample was usually taken from the mid-dorsal region, although in some of the smaller species the entire dorsal cord was used. RESULTS Table 1 shows the mean concentration (+ standard deviation) of water, cerebroside, total cholesterol and total phospholipin, and Table 2 the mean concentration of sphingomyelin, lecithin, kephalin and myelin lipid for each of the species studied. These tables can be compared with Tables 1 and 2 of the preceding paper. The figures are all given in terms of unit dry weight. In almost every instance the concentration of water is less, and the concentration of cerebroside, total cholesterol, total phospholipin, sphingomyelin and myelin lipid is greater in the spinal cord than in the brain. Lecithin and kephalin are more variable, the concentration in the brain at times exceeding that in the spinal cord. As was found for the brain, the concentration of each lipid is very similar for different individuals of the same species, but the mean concentrations of many of the lipids extend over a wide range for the different species within one class. The concentration of ester cholesterol was found to be negligibly small and is not recorded. Tables 1 and 2 also give the class mean (± standard error of mean) for the mammals, and the mean for all of the submammalian species grouped together. The significance of the differences between these two means is also given in the tables.

24 J. D. McCOLL AND R. J. ROSSITER Although the differences for both myelin lipid (sum of the cerebroside, cholesterol and sphingomyelin) and cholesterol are significant statistically, the figures for cerebroside and sphingomyelin are not. It is of interest to note, however, that the Table i. Mean concentration of water, cerebroside, total cholesterol and total phospholipin in the spinal cords of a representative series of vertebrates (The figures in brackets represent the number of individuals studied in each species.) Species Mean concentration of lipid in mg. per ioo mg. (± standard deviation) Water Cerebroside Total cholesterol dry weight Total phospholipin Elasmobranchii: Dogfish Sand shark Skate Sting ray Actinopterygii: Bowfin Menhaden Perch 2-2 ±-3 (3) 2-3 ( 2-2 ±O-O5 (3) 2-4 ±-7 (3) 2-9±o-io(3) 2-o±o-o9(4) 2-6 ±-9 (3) 15- ±-74 (6) 15-8 ±-26 (2) -4 ±-25 (4) -3 ±-51 (4) 1-9 ±-23 (6) 6-3 ±-47(6) 6-5 ±-3 (5) i2-5±i-3i (5) I5-2±O-OI (2) -4 ±-48 (4) 12-6 ±-33 (4) i2-9±o-5s (6) I5-3±O'39(6) 15-1 ±-78 (6) 256±I-II (6) 3-3 ±3 (2) 31- ±-2(4) 32±2-42 (4) 25-4± '98(6) 39-3 ±1-2 (6) 34-2 ±1-12 (6) Amphibia: Frog 4-I±O-OI (3) 19-9 ±-4 (6) IO-7±O-OI (5) 2-9 ±-33 (4) Reptilia: Turtle 2-9 ±-25 (3) 7-8 ±-87 (6) -8 ±-49(6) 27-7 ±-79 (6) Aves: Pigeon Gull 2-2 ±-1(3) 2-4±o-i3 (3) -1 ±1-1(7) -3 ±-67 (5) 12-5 ±-58 (7) n-9±o-2i (5) i8-6± 1-6(7) 22-1 ±-58 (5) Submammalia: Mean of all submammalian species(±s.e.m.) 2-6±o-i8 12-7 ±1-29 i3-4±o-47 Mammalia: Guinea-pig Rabbit Cat Class mean (±S.E.M.) 2-4 ±-5 (3) 2-1 ±-4 (3) 2-1 ±O-O4 (3) 2-2±O-IO i2-9±i-io (6) i8-3±o-26(7) 19-2 ±1-2(7) I6-8±I-97 15-6 ±-26 (6) 18-3 ±-29 (6) i8-3±o-5 3 (7) 17-4 ±-9 26-5 ±-65 (6) 32-9 ±-45 (6) 28-8 ±-86(7) P (difference between means of mammalian and submammalian species) <o-oi difference for sphingolipid (which represents the sum of the cerebroside and sphingomyelin) is significant. This is due to the inverse relation between the concentrations of cerebroside and sphingomyelin to be discussed below. In Table 3 the mean values for the lipids in both the brain and the spinal cord of each species are recorded as a percentage of the concentration of' essential lipid'. 'Essential lipid' is defined for this purpose as the sum of the cerebroside, total cholesterol and total phospholipin. The figures for brain are calculated from the data presented in Tables 1 and 2 of the previous paper (McColl & Rossiter, 1952)

Lipids of vertebrate spinal cord 25 and those for spinal cord from Tables 1 and 2 of this paper. In a number of instances where the percentage of sphingomyelin is low the percentage of cerebroside is high. This point is well illustrated in the actinopterygians. In both the brain and spinal cord of the bowfin (Order Holostei), where the percentage of cerebroside is Table 2. Mean concentration of sphingomyelin, lecithin, kephatin, and myelin lipid in the spinal cords of a representative series of vertebrates (The figures in brackets represent the number of individuals studied in each species.) Species Elasmobranchii: Dogfish Sand shark Skate Sting ray Actinopterygii: Bowfin Menhaden Perch Amphibia: Frog Reptilia: Turtle Aves: Pigeon Gull Submammalia: Mean of all submammalian species (± S.E.M.) Mammalia: Guinea-pig Rabbit Cat Class mean ( ± S.E.M.) P (difference between means of mammalian and submammalian species) Mean concentration of lipid in mg. per ioo mg. dry weight (± standard deviation) Sphingomyelin Lecithin Kephalin Myelin lipid 6-i ±55 (6) 7-3 ±o-75(2) 8-6 ±-45(4) 6-5 ±-51 (4) 3-9 ±-52 (6) 9-3±o-6o (6) 13-7 + -67(6) 5-1 ±-33(4) 7-4 ±-64 (6) 6-i ±-59 (7) 3-7 ±-24 (5) 7-1 ±-85 7-i ±-38 (6) II-5±O-6I (6) 9-6 ±-48 (7) 9-4±i-32 7-4±62 (6) 9-6 (1) 9-6 ±-17 (4) 8-5 ±i-33 (4) 8-2 ±-35(6) i3-8±i-i4(5) 12-6 ±-35(6) 8-7 ±-25 (4) 7-4 ±-37(6) 3-8 ±-42 (7) 5-8 ±-28 (5) 8-7 ±-85 5-8 ±-3 (6) 5-6±o-o8(6) 4-7 ±-34 (7) 5'4±o-34 12-1 ±-62 (6) 15-5 ( 12-8 ±-58 (4) i5-o±i-25 (4) 13-3 ± "39 (6) 15- ±-44(5) 8-3 ±-52 (6) 7-7 ±-79 (4) 12-9 ±-62 (6) 8-6 ±-72 (7) i2-6±o-6o (5) 12-2 ±-84 13-9 ± -45 (6) 16-7 ±-49 (6) -9 ±o-99 (7) 15-21-82 33-6 (6) 38-3 (1) 37-4 (4) 33-4 (4) 27-7 (6) 39 (5) 35-3 (6) 35-7 (4) 3- (6) 32-7 (7) 299 (5) 33-2 ± I-OI 35-6 (6) 48-1 (6) 47-i (7) 43-6 ±4-1 <o-oi high, the percentage of sphingomyelin is low. On the other hand, in the brain and the spinal cord of the perch (Order Teleostei), where the percentage of sphingomyelin is high, the percentage of cerebroside is low. In Fig. 1 the mean percentage of cerebroside is plotted against the mean percentage of sphingomyelin for the spinal cord of each of the species. It can be seen that the two lipids are negatively correlated(r= -635 ±-172). Each of these two lipids contains the base sphingosine. It would appear that the spinal cords of some species maintain a high concentration of one sphingosine-containing lipid at the expense of the other. Such an inverse relation is less evident in the lipids of brain. jeb.29, 2

2O6 J. D. McCOLL AND R. J. ROSSITER Table 4 gives an analysis of the results presented in Table 3. In all of tn? species studied there is a greater percentage of both myelin lipid and sphingolipid in the spinal cord than in the brain. The percentage of cerebroside in the spinal Table 3. Lipids of the brains and spinal cords of a representative series of vertebrates expressed as a percentage of 'essential lipid' Species Cerebroside Total cholesterol Sphingomyehn Lecithin Kephalin Elasmobranchii: Dogfish Sand shark Skate Sting ray Actinopterygii: Bovvfin Menhaden Perch Amphibia: Frog Reptilia: Turtle Aves: Pigeon Gull Mammalia: Guinea-pig Rabbit Cat 2-6 2-28 25-5 17-5 13-1 5-2 2O-8 1*5 18-1 2O-6 24-7 25-3 26'O 283 25-8 24-1 25-22-O 1-3 n-6 38-6 15-5 31-2 29-6 23-5 26-3 29-19- 18-3 239 17-6 22-5 21-5 22"4 16-7 21-5 28 19-1 22 22-1 22-9 23-5 247 24 22-O 26-2 25-1 27-1 28 29-4 27-6 24-6 28-4 26-4 27-5 13 17 13'S 7'3 3'o 6-4 16-6-5 69 9-9 6-5 14 9-1 98 1 n-8-4 n-3 7-9 '5-3 24-5 99-7 128 7-7 13-152 13-5 19 21-7 156 19-6 22-5 24-3 259 27-1 2O-O 18-1 191 15-7 -7 13-5 138 15-6 16-9 i6-7 22-7 22-6 16-8 -7 8-5 I2'O 1-4 8 7 31-7 46-7 27 29-4 35-38 293 25-33-8 33-3 33-8 3i-4 29-5 28-1 229 252 21-4 26-2 27-246 -8-9 25-6 19-1 26-25-3 24-1 22-4 Table 4. Analysis of data presented in Table 3 Lipid No. of species Percentage in cord less than percentage in brain Percentage in cord greater than percentage in brain No significant difference Cerebroside Total cholesterol Sphingomyelin Lecithin Kephalin Myelin lipid Sphingolipid 3 13 '4 1 13 1 1 1 cord exceeds that in the brain in 1 of the (1 not significant) species. For total cholesterol the figure is 13 out of (1 not significant), and for sphingomyelin it is out of. On the other hand, for lecithin the percentage of lipid in the brain exceeds that in the spinal cord in 13 of the (1 not significant) species, and for kephalin the figure is out of. It is thus apparent that, over the whole range of species studied, the lipids of the spinal cord, as distinct from those of the brain, are characterized by a higher percentage of cerebroside, cholesterol and sphingomyelin, and a lower percentage of lecithin and kephalin.

Lipids of vertebrate spinal cord 27 DISCUSSION It has long been known that for the mammal the spinal cord contains less water and more lipid than the brain (see Halliburton, 1894, and Fraenkel & Linnert, 191, for references). The results reported here show that the same is true over a wide range of vertebrate species. For certain lipids, however, notably lecithin and kephalin, the difference between brain and spinal cord may not be very great, and in some 2 - R V- 1 -.,SR B«r = -(H35± -172 I 1 2 Cerebroside I 3 4 Fig. 1. Relation between the concentration of cerebroside and the concentration of sphingomyelin in the spinal cords of a series of vertebrate species. The figures are expressed as a percentage of 'essential lipid'. D, dogfish; SS, sand shark; SK, skate; SR, sting ray; B, bowfish; M, menhaden; PE, perch; F, frog; T, turtle; PI, pigeon; SG, sea-gull; GP, guinea-pig; R, rabbit; C, cat. species the advantage may lie with the brain rather than with the spinal cord. Our results for the lipids of the spinal cord of mammals agree reasonably well with previously published figures, i.e. those of Brante (1949) for cerebroside, cholesterol, total phospholipin, sphingomyelin, lecithin and kephalin, and those of Samuels, Boyarsky, Gerard, Libet & Brust (1951) for total phospholipin. The inverse relation between cerebroside and sphingomyelin emphasizes the usefulness of the term sphingolipid, introduced by Carter, Haines, Ledyard & Norris (1947). These two lipids, which are not usually classified together, have a number of similar physical and chemical properties, and the present findings suggest the possibility that one may replace the other in the structure of the myelin sheath. Such a suggestion was previously made by Sadhu (1948). In this regard -2

2O8 J. D. McCOLL AND R. J. ROSSITER it is of interest to note that Williams, Galbraith, Kaucher, Mayer, Richards & Macy* (1945) reported that, expressed as a percentage of 'essential lipid', the cerebroside of rat brain increased and the sphingomyelin decreased as the animals became older. These results go further to establish the view that cerebroside, cholesterol and sphingomyelin, rather than lecithin or kephalin, are the principal lipids in the myelin sheath of a vertebrate nerve fibre. We have called these three lipids the myelin lipids. It is convenient at this time to summarize our reasons for believing that these lipids play an important part in myelin-sheath structure. (1) The white matter of mammalian brain, which contains many myelinated nerve fibres, has a higher concentration of these three myelin lipids than has grey matter, which contains comparatively few myelinated fibres (Johnson, McNabb & Rossiter, 1948a). Peripheral nerve, which is also rich in 'myelin', resembles the white matter of brain rather than the grey matter (Johnson, McNabb & Rossiter, 19486). (2) Although the distribution of lipids in the grey matter of adult brain is similar to that of the brain of newborn infants, the distribution of lipids in the white matter is very different. The white matter of adult brain, in which myelination is complete, differs from the ' white' matter of the brains of newborn infants, in which myelination is far from complete, in containing a higher concentration of these same three myelin lipids (Johnson, McNabb & Rossiter, 1949 a). (3) After section of a peripheral nerve (neurotmesis) the myelin lipids disappear from the degenerating peripheral segment at a similar rate (Johnson, McNabb & Rossiter, 1949J, 195). In a nerve regenerating after a crushing procedure that interrupts the axons and myelin sheath but leaves the connective tissue sheaths intact (axonotmesis) the myelin lipids reappear together (Burt, McNabb & Rossiter, 195). (4) The brains of mammals contain a significantly greater concentration of the myelin lipids than do the brains of lower vertebrates (McColl & Rossiter, 1951). This evidence is valid only if it is assumed (a) that the brains of mammals contain more 'myelin' than those of the lower vertebrates, and (b) that the 'myelin' of the brains of all vertebrates has a similar chemical composition. (5) It has now been shown that, for a wide variety of vertebrate species, the concentration of these three myelin lipids in the spinal cord is greater than that in the brain. Again, this evidence is valid only if (a) the spinal cord contains more 'myelin' than the brain, a reasonable assumption having regard to the microscopic structure and water content of the two tissues, and (b) the 'myelin' of the spinal cord of each species has a similar, although not necessarily an identical, chemical composition. Each of these five lines of evidence indicates that the principal lipids of the myelin sheath of a vertebrate nerve fibre are cerebroside, cholesterol and sphingomyelin. It in no way follows that these three are the only lipids contained in the myelin sheath, but they are probably those present in the greatest quantity and those that distinguish the myelin sheath from other parts of the nervous system. In no instance does the distribution of total phospholipin, lecithin, or kephalin parallel the distribution of myelin. The myelin sheath may contain some lecithin,

Lipids of vertebrate spinal cord 29 but the analyses show that considerable quantities of lecithin are also present in other non-myelin structures of the nervous system. The position of kephalin is more equivocal. Recently, Folch (1949) has shown that the 'kephalin' of the nervous system estimated by the methods used in the present study is a mixture of at least three separate lipids: phosphatidyl serine, phosphatidyl ethanolamine and brain diphosphoinositide. The exclusion of 'kephalin' from the myelin lipids does not necessarily exclude any one of the individual constituents of 'kephalin'. In fact, Brante (1949) has published data supporting the view that phosphatidyl serine is a myelin lipid. The position of phosphatidyl ethanolamine and brain disphosphoinositide is not so clear. It is to be hoped that with the development of more satisfactory analytical methods the position of 'kephalin', and of the individual constituents of 'kephalin', will be further clarified. SUMMARY 1. The concentration of water, cerebroside (glycosphingoside), free and total cholesterol, total phospholipin, monoaminophospholipin (phosphoglyceride) and lecithin (phosphatidyl choline) was determined in the spinal cords of a series of vertebrates including representatives of the cartilaginous and bony fishes, amphibians, reptiles, birds and mammals. From these figures was calculated the concentration of ester cholesterol, sphingomyelin (phosphosphingoside) and kephalin. 2. As was previously found for brain, the spinal cords of each of the species studied contained negligibly small concentrations of cholesterol ester. 3. The concentration of each lipid in the spinal cord was very similar for different individuals of the same species, but for different species within the same class the mean concentration of many of the lipids extended over a wide range. 4. The concentration of total cholesterol, sphingolipid and myelin lipid was greater in the spinal cords of mammals than in the spinal cords of the lower vertebrates. 5. Expressed as a percentage of' essential lipid', the concentration of cerebroside, cholesterol, sphingomyelin, sphingolipid and myelin lipid, but not of lecithin and kephalin, was greater in the spinal cord than in the brain. 6. For the spinal cords of the species studied, the mean concentration of cerebroside expressed as a percentage of ' essential lipid' was negatively correlated with the mean concentration of sphingomyelin. 7. The results are discussed in relation to the chemical nature of the lipids of the myelin sheath of a vertebrate nerve fibre. This work was aided by grants from the National Research Council of Canada and the Dominion Mental Health Grants. Dr R. C. Buck, Mr N. S. Burt, Mr G. Jaciw and Miss Ann Boyce rendered technical assistance. Thanks are due to the Director, Marine Biological Laboratory, Woods Hole, for making the facilities of the laboratory available to one of us (J. D. McC.) during the tenure of a National Research Council Summer Scholarship.

21 J. D. McCOLL AND R. J. ROSSITER REFERENCES BRANTE, G. (1949). Acta physiol. scand. 18 (Suppl.), no. 63, p. 1. BURT, N. S., MCNABB, A. R. & ROSSITER, R. J. (195). Biochem. J. 47, 318. CARTER, H. E. ( HAINES, W. J., LEDYARD, W. E. & NORRIS, W. P. (1947). J. Biol. Chem. 169,77. FOLCH, J. (1949). J. Biol. Chem. 177, 497. FRAENKEL, S. & LINNERT, K. (191). Biochem. Z. 36, 44. HALIJBURTON, W. D. (1894). J. Physiol. 15, 9. JOHNSON, A. C, MCNABB, A. R. & ROSSITER, R. J. (1948a). Biochem. J. 43, 573. JOHNSON, A. C, MCNABB, A. R. & ROSSITER, R. J. (19486). Biochem. J. 43, 578. JOHNSON, A. C, MCNABB, A- R. & ROSSITER, R. J. (1949a). Biochem. J. 44, 494. JOHNSON, A. C, MCNABB, A. R. & ROSSITER, R. J. (19496). Biochem. J. 4s, 5. JOHNSON, A. C, MCNABB, A. R. & ROSSITER, R. J. (195). Arch. Neurol. Ptychiat., Chicago. 64, 15. MCCOLL, J. D. & ROSSITER, R. J. (1951). J. Exp. Biol. 29, 196. SADHU, D. P. (1948). J. Dairy Set. 31, 347. SAMUELS, A. J., BOYARSKY, L. L., GERARD, R. W., LIBET, B. & BRUST, M. (1951). Amer. J. Physiol. 164, 1. WILLIAMS, H. H., GALBRAITH, H., KAUCHER, M., MOVER, E. Z., RICHARDS, A. J. & MACY, I. G. (1945). J. Biol. Chem. 161, 475.