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Biological Research

Print version ISSN 0716-9760

Biol. Res. vol.38 no.4 Santiago  2005

http://dx.doi.org/10.4067/S0716-97602005000400006 

Biol Res 38: 347-352, 2005

ARTICLE

Central actions of somatostatin in the generation and control of breathing

Isabel Llona and Jaime Eugenín

Laboratory of Neural Systems, Department of Biology, Universidad de Santiago de Chile, Santiago, Chile

Dirección para correspondencia


ABSTRACT

The neuropeptide somatostatin is involved in many functions in the central nervous system as well as in the periphery. When it is centrally injected, an irreversible apnea is often developed. In the present review, we discuss the effects of somatostatin as the result of its actions at three levels of the respiratory neural network: a) by modulating the output of cranial or spinal motoneurons; b) by altering the genesis of the respiratory rhythm in the brainstem; and c) by regulating the chemosensory drive input into the respiratory pattern generator.

Key terms: apnea, brainstem, chemoreceptors, respiratory rhythm.


 

The respiratory pattern generator (RPG) is a neuronal network localized in the brainstem responsible for generating the pattern of repetitive motor activity necessary for breathing. The efferent pathway of the RPG commands the cranial and spinal motoneurons that innervate the respiratory muscles. The RPG integrates information from many areas of the CNS, including the cortex, hypothalamus, cerebellum, pons and medulla, and receives information about basic sensory modalities from pulmonary mechanoreceptors as well as central (Nattie, 1999) and peripheral chemoreceptors (Zapata & Larraín, 2005). As the result of these multiple interactions, breathing is a highly regulated process constrained by allometric (Günther & Morgado, 2003) and optimization rules (Tehrani, 2003).

Somatostatin (SST) was first identified as a hypothalamic factor, which inhibits the release of growth hormone from anterior pituitary (Brazeau et al., 1973). Both SST and its receptors (SSTR) were subsequently found distributed in several extra-hypothalamic areas of the central nervous system (Finley et al., 1981; Johanson et al., 1984; Moller et al., 2003) and the periphery (Lewin, 1992) in the adult as well as in the developing organism. The widespread distribution of SST suggests that SST is involved in multiple biological functions. The site and dose of SST administration are critical for revealing its respiratory effects. In contrast to earlier works (Niewoehner et al., 1983), Kalia et al. (1984) found that injection of 6 nmol of SST in the cisterna magna of anaesthetized rats produces apnea that was usually irreversible. Actual evidence shows that SST may affect respiration via mechanisms operating at three distinct levels of the central respiratory network: a) by modulating the output of cranial and spinal motoneurons; b) by altering respiratory rhythmogenesis in the brainstem; and c) by regulating the chemosensory drive to the RPG. We will summarize some of the evidence on the localization of SST in the brainstem before we review the evidence on central actions of SST at these three levels.

SOMATOSTATIN LOCALIZATION IN THE BRAINSTEM RESPIRATORY GROUPS

Mammalian forebrain and hypothalamic areas contain a relatively large amount of SST, while lower brainstem contains a small amount of SST. In the brainstem, SST can be detected in somata and terminals of several nuclei related to the central respiratory groups (Kalia et al., 1984; Leibstein et al., 1985; Llona et al., 2001; Stornetta et al., 2003), the auditory central pathways (Wynne et al., 1995; Kungel & Friauf, 1995) and brainstem nuclei related to autonomic regulation, like the parabrachial nucleus or the nucleus of tractus solitarius (NTS) (Block & Hoffman, 1987; Saha et al., 2002). As other neuropeptides (Najimi et al., 2001), the level of expression of SST varies with the age of the animal. Numerous SST-positive structures in the lower brainstem have been detected in the neonatal rat, but not in the adult rat (Shiosaka et al., 1981; Fitzpatrick-McElligott, et al., 1991; Kungel and Friauf, 1995).

Using in situ hybridization, Shiraishi et al. (1993) were able to detect SST mRNA in the brainstem of adult rats in the same areas where it is found in the neonatal period, suggesting that some expression of the gene is present in the adult stage. Also, SSTR show transient appearance in several brain regions, for example SSTR4 (SST receptor type 4) is expressed transiently and successively replaced by SSTR1 in the brainstem of the neonatal rat (Wulfsen et al., 1993). The first report that SST was present in neurons and terminals of the pre-Bötzinger complex, a nuclei localized in the ventrolateral medulla and proposed to be the site of respiratory rhythm generation (Feldman et al., 2003; Smith et al., 1991), was obtained in the newborn mouse (Llona et al., 2001). Recently, Stornetta et al. (2003) showed in the adult rat that SST-positive neurons in the pre-Bötzinger complex also contain glutamate as neurotransmitter. It is possible that pre-synaptic SST actions could play a role modulating glutamate release in the pre-Bötzinger. In other glutamatergic terminals, like cerebrocortical nerve endings, SST through activation of pre-synaptic sst2 receptors inhibits the adenylyl cyclase-protein kinase A pathway, which, in turn, reduces the glutamate release (Grilli et al., 2004).

The temporal and spatial patterns of expression of SST and SSTR suggest that SST plays a role in specific brain areas during restricted and precise periods of the development of the nervous system. In has been described that depletion of SST during early development affects the branching density of the dendrites in the rat's lateral superior olive, an auditory brainstem nucleus (Kungel et al., 1997), suggesting that the peptide can exert a trophic role during the neurogenesis and synaptogenesis of the lower brainstem. On the other hand, an abnormal persistence of the density of binding sites to SST at high levels have been detected in the brainstem of infants who died from Sudden Infant Death Syndrome (SIDS), the primary cause of death in human infants aged between 1 and 12 months in industrialized countries (Carpentier et al., 1998). In this syndrome, a defect in the neuroregulation of the cardiorespiratory system is strongly suspected (Kinney et al., 2001) and a high frequency of episodes of prolonged central apneas have been reported in infants who subsequently died of SIDS (Schechtman et al., 1991).

As far as localization is concerned, SST may exert a role in the generation and or control of respiration because both the peptide and its receptors are present in the respiratory groups of the brainstem.

ACTION OF SST ON RESPIRATION

As mentioned before, Kalia et al. (1984) found that injection of SST in the cisterna magna of anaesthetized rats produces apnea that was usually irreversible. The site of action of SST was suggested to be the dorsal respiratory neurons. When the injection site was more clearly defined, it was found that SST injected in the ventrolateral medulla, in particular in the nucleus paragigantocellularis lateralis of cats and rats, consistently caused apnea (Yamamoto et al., 1988; Chen et al., 1990) suggesting that SST contributes to the central regulation of respiration acting at some critical point within the ventral respiratory group. In the rat, SST and Substance P have antagonistic effects on respiratory regulation in medulla oblongata (Chen et al., 1991). SST-induced apnea can be prevented by central and peripheral administration of an opiate receptor antagonist, like naloxone (Harfstrand et al., 1985), suggesting that SST-induced apnea is mediated by activation of opioid receptors. Aspartic acid depression of ventilation has been suggested to be due to release of SST, but it is not clear if this is a peripheral or central action (Schenker & Hoffman, 1996).

SST INTERACTION WITH MOTONEURONS

For a direct interaction between SST and motoneurons, the presence of SSTR located on the motoneurons is a requisite. There are some pieces of evidence pointing in this direction. For example, SSTR2 has been detected in rat nucleus ambiguous and hypoglossal motor nucleus (Breder et al., 1992). In rat lumbar motoneurons, SSTR3 has been detected (Segond von Banchet et al., 1999), and by in situ hybridization, the mRNA for SSTR3 was visualized in motoneurons of cranial nerves, including the facial and the hypoglossal nuclei (Señaris et al., 1995). However, binding of SST could not be detected (Reubi & Maurer, 1985; Uhl et al., 1985) by autoradiography at this level. Low to moderate concentrations of SST-positive nerve endings are found surrounding the motor cranial nerve nuclei (Johansson et al., 1984). Although SSTR- and SST-positive nerve endings have been described in the respiratory motoneurons of the brainstem, and SST hyperpolarizes vagal motoneurons (Oomura & Mizuno, 1986), the possibility that SST-induced apnea is due, in part, to interaction with the cranial motoneurons remains to be elucidated.

INTERACTION WITH RPG

With regard to the generation of the respiratory rhythm, SST-positive neurons could be part of the network that generates the respiratory rhythm or be neuromodulators. SST is present in inspiratory neurons of the pre-Bötzinger complex (Llona et al., 2001; Stornetta et al., 2003), the proposed site of respiratory rhythm generation. This localization suggests that SST is in neurons belonging to the RPG. However, SST is not essential for the generation of the rhythm, because null mutant mice lacking somatostatin seem healthy, fertile, and superficially indistinguishable from their heterozygous and wild-type littermates (Zeyda et al., 2001). The presence of SSTR in the pre-Bötzinger complex has not been determined, and the projections of the SST neurons into this nucleus are not yet defined.

INTERACTION WITH CHEMOSENSORY DRIVE

The SST administration in the ventrolateral medulla resulted in a blunted ventilatory response to hypoxia and hypercapnia (Chen et al., 1990). Moreover, hypoxia and hypercapnia shortened the latency of SST-induced apnea, indicating an interaction between chemoreception and SST actions (Harfstrand et al., 1984).

In humans, intravenous infusion of SST greatly reduces the ventilatory response to hypoxia without changing the ventilatory response to hypercapnia (Maxwell 1986; Filuk 1988). In both studies, a central effect cannot be discarded because very high doses were used and some SST can cross the brain blood barrier (Banks et al., 1990). SST has been localized within nerve fibers innervating the arterial chemoreceptor (Kummer, 1989; Kameda, 1989) and inhibits whole cell calcium currents recorded from chemoreceptor glomus (type 1) cells from rat carotid bodies (e Silva, 1995). These results, together with those of Pedersen et al. (1999), suggest that the most likely site of action of SST on hypoxic ventilatory response is the carotid body. On the other hand, under chronic hypoxia, SST gene expression is unchanged (Mosqueira et al., 2004), suggesting that it most likely does not contribute to the functional changes induced by hypoxia (Del Río et al., 2004). The ventilatory response to CO2 was not modified by peripheral administration of octreotide, an analogue of SST (Cao et al., 1998), pointing to a central interaction between SST and chemoreception.

In vitro preparations of the central nervous system have been useful for studying mechanisms of breathing control by central chemoreceptors (Nattie, 1999; Eugenín et al., 2001). Using the neonatal mouse medullary-spinal cord preparation, we showed that the interaction between SST and hypercapnia occurs at the central level (Llona et al., 2004). Somatostatin decreased both frequency and amplitude of fictive respiration. The inhibition of respiratory frequency was greater during acidification of the medium than in basal conditions. SST depression of respiration does not seems to depend on the basal state of the respiratory network, because it was not correlated with the basal frequency of the preparation or with the age of the pup from which the brainstem was obtained. At the present time, it is unclear how SST and the chemosensory input may interact within the brainstem to regulate respiration. In our preparation, influences from pontine respiratory groups or peripheral chemoreceptors were absent. Therefore, the actions of SST on respiration are probably at the level of the dorsal and/or ventral respiratory groups of the medulla.

In addition, there is some interaction between chemoreceptors and SST in the control of the tracheal wall tension. The tracheal tension decreased as well as the phrenic nerve activity when SST was applied to the surface of ventral medulla in animals that were hypercapnic (Haxhiu et al., 1993a). Also, application of SST to the surface of the ventral medulla attenuated the response to hypoxia, decreasing the tracheal pressure response. Both effects were abolished after muscarinic blockade suggesting an indirect effect of the peptide. Thus, SST administered in the surface of the ventral medulla modulates parasympathetic outflow to the airway smooth muscle.

The origin of SST in the surface of the ventral medulla may be, at least in part, in the paraventricular and lateral hypothalamic areas that project to the ventrolateral medulla including the airway-related vagal preganglionic neurons (Haxhiu, 1993b).

In summary, these results point to a interaction between SST and central chemoreception in the control of breathing. Several nuclei have been demonstrated to have chemosensory properties (Nattie, 1999), and they can be considered as candidates for localizing the neural circuits where these interactions take place. The SST effects on hypoxic response are most probably of peripheral origin (carotid bodies), while on the contrary, the SST interaction with the chemosensory drive takes place somewhere at the ventral respiratory group of the brainstem.

CONCLUSIONS

SST acting at different levels within the central nervous system contributes to the control of respiration. Although this neuropeptide is not crucial for rhythm generation, it is involved in the modulation of the respiratory rhythm. This modulation is in part related to the interaction between SST and central chemoreception, through which, SST can influence an important tonic input driving respiration.

ACKNOWLEDGEMENTS

This work was supported by Fondecyt #100025 and DICYT #020343LL. This article is dedicated to Dr. Patricio Zapata who inspired many generations of students during his course of neurophysiology.

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Corresponding author: Dr. Isabel Llona, Laboratorio de Sistemas Neurales, Depto. Biología, Facultad de Química y Biología, Universidad de Santiago de Chile, Casilla 40, Correo 33, Santiago, Chile, Fax: (56-2) 681-2108, E-mail: illona@lauca.usach.cl

Received: May 19, 2005. Accepted: June 4, 2005.

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