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Primary cellular mechanism driving protoplasmic streaming in Amoeba
Flow of cytoplasm mediated by pseudopodia and cytoskeletal microfilaments.
Dual physiological functions performed by cilia in Paramecium
Locomotion through the aquatic medium and propulsion of food particles through the cytopharynx.
Dual functions served by tentacles in Hydra
Capturing prey and facilitating locomotion.
Fundamental rule governing the relationship between movement and locomotion
All locomotions are movements, but all movements are not locomotions.
Specialized human blood cells capable of amoeboid movement
Macrophages and leucocytes.
Cytoskeletal elements directly involved in driving amoeboid movement
Microfilaments composed of actin.
Two anatomical locations in the human body lined by ciliated epithelium that perform ciliary movement
Respiratory tract (trachea) for clearing inhaled dust particles, and the female reproductive tract (fallopian tubes) for passage of ova.
Three biological systems exhibiting flagellar movement
Swimming of spermatozoa, maintenance of water currents in sponge canal systems, and locomotion in Protists like Euglena.
Three organ systems whose coordinated activity is indispensable for locomotion
Muscular, skeletal, and neural systems.
Embryonic germ layer of origin for muscular tissue
Mesoderm.
Percentage of total body weight contributed by muscular tissue in an adult human
40–50%.
Total number of muscles in an adult human and their distribution
639 muscles in total, comprising 317 paired muscles and 5 unpaired muscles.
Four cardinal physiological properties of muscle tissue
Excitability, contractility, extensibility, and elasticity.
Functional property shared by both muscle cells and nerve cells
Excitability.
Mechanism responsible for muscular enlargement during life
Hypertrophy (increase in muscle fibre size), as hyperplasia (increase in cell number) is absent post-embryonic development.
Histological, structural, and regulatory properties of skeletal muscle fibres
Striated, voluntary, cylindrical, unbranched, and multinucleated (syncytium) with peripheral nuclei.
Histological, structural, and regulatory properties of visceral (smooth) muscle fibres
Non-striated, involuntary, spindle-shaped (fusiform), unbranched, and uninucleated with a central nucleus.
Histological, structural, and regulatory properties of cardiac muscle fibres
Striated, involuntary, cylindrical, branched, uninucleated with a central nucleus, and fatigue-resistant.
Specialized cell junctions in cardiac tissue that enable synchronized contraction
Intercalated discs equipped with gap junctions.
Relative contraction speed ranking among the three muscle types
Cardiac is fastest, skeletal is fast, and visceral (smooth) is slowest.
Vascular supply comparison among skeletal, smooth, and cardiac muscles
Cardiac has abundant blood vessels, skeletal has rich blood vessels, and smooth has less blood vessels.
Common collagenous connective tissue layer holding multiple muscle bundles or fascicles together
Fascia.
Connective tissue sheath enclosing an entire individual muscle organ
Epimysium.
Connective tissue sheath surrounding an individual muscle fascicle
Perimysium.
Delicate connective tissue sheath investing a single muscle fibre
Endomysium.
Plasma membrane lining an individual muscle fibre
Sarcolemma.
Cytoplasm of a muscle fibre and its primary storage molecules
Sarcoplasm, containing glycogen granules and myoglobin.
Organelle serving as the primary intracellular reservoir for calcium ions in muscle fibres
Sarcoplasmic reticulum.
Parallel protein filaments arranged longitudinally within muscle sarcoplasm
Myofilaments or myofibrils.
Protein constituting the dark, anisotropic band in myofibrils
Myosin (forming the A-band).
Protein constituting the light, isotropic band in myofibrils
Actin (forming the I-band).
Optical property of the light band under polarized light
Mono-refractive (isotropic).
Elastic fibrous membrane that bisects each I-band and anchors thin filaments
Z-line (Krause membrane).
Thin fibrous membrane running through the middle of the A-band that holds thick filaments together
M-line.
Central zone of thick filaments not overlapped by thin filaments in a resting state
H-zone (Hensen zone).
Functional and structural unit of muscle contraction
Sarcomere, spanning the region between two successive Z-lines.
Band composition formula representing a single relaxed sarcomere
21 I-band+1 A-band+21 I-band.
Structural composition of the thin (actin) filament
Two filamentous 'F'-actins helically wound together, along with two strands of tropomyosin and periodically spaced troponin complexes.
Monomeric building block of F-actin
Globular actin ('G'-actin), which polymerizes in the presence of Mg2+.
Fibrous regulatory protein running close to F-actin throughout its length to mask myosin-binding sites at rest
Tropomyosin.
Three functional subunits composing the troponin complex
TpT (binds tropomyosin), TpI (inhibits actin-myosin interaction by masking active sites), and TpC (binds calcium ions).
Monomeric protein subunit constituting thick myosin filaments
Meromyosin, with approximately 300 monomers assembling into one thick filament.
Structural components constituting Heavy Meromyosin (HMM)
Globular head and short arm, which together project outward as the cross-arm.
Structural component constituting Light Meromyosin (LMM)
The straight fibrous tail portion of the meromyosin monomer.
Two specific binding sites located on the globular head of meromyosin
Actin-binding site and ATP-binding site.
Enzymatic catalytic capability located within the globular head of meromyosin
ATPase enzyme activity.
Biologists who formulated the Sliding Filament Theory
A. Huxley and H. Huxley.
Central premise of the Sliding Filament Theory
Contraction of a muscle fibre takes place by the sliding of thin filaments over thick filaments without shortening of individual filaments.
Components of a single physiological motor unit
A single motor neuron along with all the muscle fibres it innervates.
Junction between a somatic motor neuron axon terminal and the muscle sarcolemma
Neuromuscular junction or motor end-plate.
Neurotransmitter discharged into the synaptic cleft at the motor end-plate
Acetylcholine (ACh).
Membrane channel opened by acetylcholine binding on the sarcolemma
Ligand-gated sodium (Na+) channels, inducing depolarization.
Tubular invaginations of the sarcolemma that conduct action potentials deep into the sarcoplasm
T-tubules (transverse tubules).
Immediate trigger for the unmasking of active sites on actin filaments
Binding of calcium (Ca2+) to the TpC subunit of troponin.
Molecular bond established when energized myosin binds to exposed actin sites
Actin-myosin cross-bridge.
Mechanical event wherein the myosin head tilts and pulls actin towards the centre of the A-band
Power stroke.
Dimensional change in the A-band during full muscle contraction
The A-band retains its original length and does not shorten.
Dimensional changes in the I-band and H-zone during muscle contraction
The I-band reduces in width and the H-zone shortens or completely disappears.
Movement of Z-lines during sarcomere shortening
Successive Z-lines are pulled inwards towards each other.
Molecular event responsible for detaching the myosin head from actin to break the cross-bridge
Binding of a new ATP molecule to the myosin head.
Products released from the myosin head during the execution of the power stroke
ADP and inorganic phosphate (Pi).
Active transport mechanism essential for restoring the muscle fibre to its relaxed state
Active pumping of Ca2+ from the sarcoplasm back into the sarcoplasmic reticulum cisternae via Ca2+ ATPase pumps.
Enzymatic degradation terminating acetylcholine action at the motor end-plate
Cleavage into acetate and choline by acetylcholinesterase.
Immediate biochemical source of energy consumed during muscle contraction cycles
Adenosine triphosphate (ATP).
Number of ATP molecules hydrolyzed per individual cross-bridge interaction cycle
1 molecule of ATP.
Metabolic consequence of repeated muscle contraction leading to fatigue
Anaerobic breakdown of glycogen leading to the accumulation of lactic acid.
Chemical cause of post-mortem rigor mortis
Depletion of cellular ATP, preventing the detachment of myosin heads from actin and locking muscles in contracture.
Red, iron-containing, oxygen-storing pigment present in muscle sarcoplasm
Myoglobin.
Biochemical and physiological features of Red muscle fibres
High myoglobin, abundant mitochondria, dense capillary beds, low sarcoplasmic reticulum, smaller diameter, and aerobic sustained contractions resistant to fatigue.
Biochemical and physiological features of White muscle fibres
Low myoglobin, few mitochondria, sparse capillary beds, abundant sarcoplasmic reticulum, larger diameter, and fast anaerobic twitches that fatigue quickly.
Anatomical example of muscles rich in red fibres in humans
Extensor muscles of the back (postural muscles).
Anatomical example of muscles predominantly composed of white fibres in humans
Eyeball muscles.
Chemical difference distinguishing bone matrix from cartilage matrix
Bone matrix is hard and non-pliable due to calcium salts, whereas cartilage matrix is slightly pliable due to chondroitin salts.
Total bone count in a normal adult human skeleton versus a newborn
206 bones in an adult versus approximately 305–306 bones in a newborn.
Scientific study of bone structure and skeletal system disorders
Osteology (or skeletology).
Scientific study of muscular structure, function, and pathology
Myology (or sarcology).
Total number of bones comprising the adult axial skeleton
80 bones.
Four skeletal regions constituting the axial skeleton
Skull, vertebral column, ribs, and sternum.
Total number of bones comprising the appendicular skeleton
126 bones.
Skeletal components constituting the appendicular skeleton
Bones of the limbs (120) and their supporting girdles (6).
Total number of bones in the human skull excluding the hyoid and ear ossicles
22 bones (8 cranial bones and 14 facial bones).
Bone count and inventory of the human cranium (brain box)
8 bones: 1 frontal, 2 parietal, 2 temporal, 1 occipital, 1 sphenoid, and 1 ethmoid.
Saddle-shaped depression in the sphenoid bone that houses the pituitary gland
Sella turcica.
Large posterior aperture of the occipital bone through which the medulla oblongata continues as the spinal cord
Foramen magnum.
Two rounded cranial articular projections that articulate with the first cervical vertebra
Occipital condyles.
Vertebrate groups characterized by a dicondylic skull
Mammals and amphibians.
Vertebrate groups characterized by a monocondylic skull
Fishes, reptiles, and birds.
Bone count and inventory of the human facial skeleton
14 bones: 2 nasal, 2 maxillae, 2 zygomatic, 2 lacrimal, 2 palatine, 2 inferior nasal conchae, 1 vomer, and 1 mandible.
Largest, strongest, and only movable bone of the human face
Mandible.
Triangular unpaired facial bone forming the inferior and posterior part of the nasal septum
Vomer.
Anatomical characteristics and muscular attachment of the hyoid bone
Single U-shaped bone located at the base of the buccal cavity that does not articulate with any other bone and anchors the tongue.
Three middle ear ossicles arranged in sequence from outer to inner ear
Malleus, Incus, and Stapes.
Morphological shapes corresponding to the malleus, incus, and stapes
Hammer-shaped (malleus), anvil-shaped (incus), and stirrup-shaped (stapes).
Smallest bone present in the human body
Stapes.
Total number of ear ossicles in the human body
6 bones (3 in each middle ear cavity).
Total number of vertebrae in the human vertebral column during infancy versus adulthood
33 vertebrae in infants, reducing to 26 functional bones in adults due to fusion.
Adult human vertebral formula
C7T12L5S(5)Co(4)=26 vertebrae.
First cervical vertebra (C1) and its primary articulating function
Atlas, which articulates with the occipital condyles to support the skull and facilitate nodding ('yes') movements.
Second cervical vertebra (C2) and its distinctive articulating process
Axis, possessing an odontoid process (peg) that forms a pivot joint with the atlas for head rotation ('no' movement).
Number of cervical vertebrae present in almost all mammals
7 cervical vertebrae.