Rostral to the midbrain lies the forebrain (prosencephalon, cerebrum; see Fig. 1.13 ). The forebrain consists of the bilaterally paired diencephalon and cerebral hemisphere on each side and is by far the largest derivative of the three basic embryological divisions of the brain. The diencephalon is continuous with the rostral part of the midbrain and lies between the brainstem and the cerebral hemisphere. From dorsal to ventral, the diencephalon is comprised of the epithalamus, thalamus, subthalamus and hypothalamus, of which the thalamus is the largest. The thalamus consists of numerous nuclei, most of which have extensive reciprocal connections with the cerebral cortex. Of particular note are:

  • Nuclei that transmit general and special sensory information to corresponding regions of the sensory cortices

  • Nuclei that receive impulses from the cerebellum and basal ganglia and interface with motor regions of the frontal lobe

  • Nuclei that have connections with associative and limbic areas of the cerebral cortex

The diencephalon is almost entirely surrounded by the cerebral hemisphere; consequently, little of its structure can be seen externally, apart from the ventral portion of the hypothalamus , which can be seen on the base of the brain ( Fig. 12.1 ). Immediately caudal to the optic chiasm is a small midline elevation, the tuber cinereum . From its apex extends the infundibulum or pituitary stalk, which attaches to the pituitary gland. Caudal to the tuber cinereum, a pair of rounded eminences, the mammillary bodies, are located on either side of the midline. These contain the mammillary nuclei of the hypothalamus. The hypothalamus lies below the thalamus, extending medial and ventral to the subthalamus. It has important connections with the limbic system, a controlling influence upon the activity of the autonomic nervous system and a central role in neuroendocrine function, partly through its relationship with the pituitary gland. The hypothalamus is discussed further in Chapter 16 .

Fig. 12.1
Ventral aspect of the diencephalon.

The other parts of the diencephalon can be seen in sagittal and coronal sections of the brain ( Figs 12.2, 12.3 ). The diencephalon forms the lateral wall of the third ventricle. The dorsal part of the ventricular wall is formed by the thalamus and the ventral part by the hypothalamus. The epithalamus is a relatively small part of the diencephalon located, in its most caudal and dorsal region, immediately rostral to the superior colliculus of the midbrain. It consists principally of the pineal gland and the habenula ( habenular nuclei ). The pineal gland ( Fig. 12.2 and see Fig. 13.12 ) is an endocrine organ. It synthesises the hormone melatonin. The pineal gland has been implicated in control of the sleep/waking cycle (circadian rhythm) and in regulation of the onset of puberty. The habenula (habenular nuclei; Fig. 12.2 and see Fig. 13.11 ) has connections with the limbic system ( Chapter 16 ).

Fig. 12.2
Median sagittal section of the brain showing the relationships of the diencephalon.

Fig. 12.3
(A,B) Coronal sections through the diencephalon.
Luxol fast blue stain for myelin.

The subthalamus lies beneath the thalamus and dorsolateral to the hypothalamus, with its ventrolateral aspect against the internal capsule. It contains two notable cell groups, the subthalamic nucleus and the zona incerta . The subthalamic nucleus is located in the ventrolateral part of the subthalamus, immediately medial to the internal capsule (see Figs 13.9 , 14.8 ). It has the shape of a biconvex lens in coronal section. The subthalamic nucleus has prominent connections with the globus pallidus and the substantia nigra and is important in the control of movement. It is discussed in more detail in Chapter 14 . The zona incerta is a rostral extension of the brainstem reticular formation. Several important fibre systems traverse the subthalamus en route to the thalamus. These include ascending sensory projections (medial lemniscus, spinothalamic tracts, trigeminothalamic tracts), cerebellothalamic fibres from the dentate nucleus and pallidothalamic fibres from the internal segment of the globus pallidus. The latter group of fibres envelop the zona incerta as the lenticular fasciculus and thalamic fasciculus (see Fig. 14.8 ).

Topographical anatomy of the thalamus

External features

The thalamus has been likened in size and shape to a small hen's egg. Together with the hypothalamus, it forms the lateral wall of the third ventricle, the transition between the two being marked by a faint groove, the hypothalamic sulcus. In most individuals, the two thalami are joined across the thin slit of the ventricle by the interthalamic adhesion or massa intermedia . A fascicle of nerve fibres, the stria medullaris ( thalami ), which has limbic connections, courses along the dorsomedial margin of the thalamus ( Fig. 12.2 ). Along this line, the ependymal lining of the third ventricle spans the narrow lumen to form the ventricular roof.

The anterior pole of the thalamus extends as far as the interventricular foramen, through which the third and lateral ventricles are in continuity. Lateral to the thalamus lies the posterior limb of the internal capsule and anterolateral lies the head of the caudate nucleus ( Fig. 12.4 ). The dorsal aspect of the thalamus thus forms part of the floor of the body of the lateral ventricle. Another fascicle of nerve fibres with limbic connections, the stria terminalis , marks the boundary between thalamus and caudate ( Figs 12.3B, 12.4 ). Ventral to the thalamus lie the subthalamus and hypothalamus; caudal to it lies the midbrain.

Fig. 12.4, Dorsal aspect of the diencephalon.

Internal organisation

Within the thalamus is located a thin layer of nerve fibres composed of some of the afferent and efferent connections of thalamic nuclei. This is called the internal medullary lamina ( Figs 12.3, 12.5, 12.6 ). The lamina is roughly Y-shaped when viewed from above and provides the basis for dividing the main part of the thalamus into three nuclear masses: anterior , medial and lateral . Each of these cellular complexes is further subdivided into a number of individually named nuclei. The lateral nuclear group, in particular, has important connections with sensory and motor regions of the cerebral cortex. Embedded within the internal medullary lamina are several cell groups, known collectively as the intralaminar nuclei ( Fig. 12.5 ). Lateral to the main mass of thalamic nuclei lies another sheet of nerve fibres, the lateral medullary lamina ( Fig. 12.3B ), which consists of thalamocortical and corticothalamic fibres. Between this and the internal capsule is located a thin stratum of neurones that constitute the reticular nucleus of the thalamus ( Fig. 12.3B ).

Anatomy of the thalamus

  • The thalamus is the largest component of the diencephalon, which is situated between the brainstem and the cerebral hemisphere.

  • Almost all thalamic nuclei have rich reciprocal connections with the cerebral cortex.

  • The thalamus is divided into three principal nuclear masses (anterior, medial and lateral) by the internal medullary lamina. The lateral nuclear group have connections with sensory and motor cortices.

  • Embedded within the internal medullary lamina lie intralaminar nuclei.

  • On the lateral aspect of the thalamus lies the thin reticular nucleus.

Fig. 12.5, The left thalamus viewed from the anterolateral aspect (A,C) and in coronal section (B,D), showing the principal nuclear groups (A,B) and the divisions of the lateral nuclear group (C,D).

Fig. 12.6, Organisation of thalamic nuclei and their principal relationships with the cerebral cortex.

Functional organisation of thalamic nuclei

All the nuclei of the thalamus, with the exception of the reticular nucleus, project to the ipsilateral cerebral cortex and the whole of the cortex receives input from the thalamus. Similarly, all thalamic nuclei receive corticofugal fibres that are ordered in a basically reciprocal fashion. In some cases, precise, point-to-point projections exist between individual thalamic nuclei and restricted cortical zones with well-defined sensory or motor functions. This organisation typifies the relationship between the thalamic nuclei and cortical regions that subserve the general and special senses and the motor regions that receive cerebellar and basal ganglia input ( Fig. 12.6 ). Such thalamic nuclei are often referred to as the ‘ specific nuclei .

The specific nuclei all lie within the ventral part (tier) of the lateral nuclear group. Other thalamic nuclei receive less functionally distinct afferent input that does not include overtly sensory or motor pathways; in turn, these connect with wider areas of cortex, including associative and limbic domains. These are often referred to as the ‘ non-specific nuclei . Non-specific thalamic nuclei include the nuclei of the dorsal tier of the lateral nuclear complex as well as the whole of the anterior and medial complexes.

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