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1.
PLoS Genet ; 11(2): e1004935, 2015 Feb.
Article in English | MEDLINE | ID: mdl-25671638

ABSTRACT

Cell-specific expression of many genes is conveyed by multiple enhancers, with each individual enhancer controlling a particular expression domain. In contrast, multiple enhancers drive similar expression patterns of some genes involved in embryonic development, suggesting regulatory redundancy. Work in Drosophila has indicated that functionally overlapping enhancers canalize development by buffering gene expression against environmental and genetic disturbances. However, little is known about regulatory redundancy in vertebrates and in genes mainly expressed during adulthood. Here we study nPE1 and nPE2, two phylogenetically conserved mammalian enhancers that drive expression of the proopiomelanocortin gene (Pomc) to the same set of hypothalamic neurons. The simultaneous deletion of both enhancers abolished Pomc expression at all ages and induced a profound metabolic dysfunction including early-onset extreme obesity. Targeted inactivation of either nPE1 or nPE2 led to very low levels of Pomc expression during early embryonic development indicating that both enhancers function synergistically. In adult mice, however, Pomc expression is controlled additively by both enhancers, with nPE1 being responsible for ∼80% and nPE2 for ∼20% of Pomc transcription. Consequently, nPE1 knockout mice exhibit mild obesity whereas nPE2-deficient mice maintain a normal body weight. These results suggest that nPE2-driven Pomc expression is compensated by nPE1 at later stages of development, essentially rescuing the earlier phenotype of nPE2 deficiency. Together, these results reveal that cooperative interactions between the enhancers confer robustness of Pomc expression against gene regulatory disturbances and preclude deleterious metabolic phenotypes caused by Pomc deficiency in adulthood. Thus, our study demonstrates that enhancer redundancy can be used by genes that control adult physiology in mammals and underlines the potential significance of regulatory sequence mutations in common diseases.


Subject(s)
Embryonic Development/genetics , Enhancer Elements, Genetic/genetics , Evolution, Molecular , Pro-Opiomelanocortin/biosynthesis , Regulatory Sequences, Nucleic Acid/genetics , Animals , Conserved Sequence , Female , Gene Expression Regulation, Developmental , Mammals/genetics , Mice , Neurons/metabolism , Phylogeny , Pregnancy , Pro-Opiomelanocortin/deficiency , Pro-Opiomelanocortin/genetics
2.
Endocrinology ; 156(3): 1052-65, 2015 Mar.
Article in English | MEDLINE | ID: mdl-25551181

ABSTRACT

Distinct male and female patterns of pituitary GH secretion produce sexually differentiated hepatic gene expression profiles, thereby influencing steroid and xenobiotic metabolism. We used a fully automated system to obtain serial nocturnal blood samples every 15 minutes from cannulated wild-type (WT) and somatostatin knockout (Sst-KO) mice to determine the role of SST, the principal inhibitor of GH release, in the generation of sexually dimorphic GH pulsatility. WT males had lower mean and median GH values, less random GH secretory bursts, and longer trough periods between GH pulses than WT females. Each of these parameters was feminized in male Sst-KO mice, whereas female Sst-KO mice had higher GH levels than all other groups, but GH pulsatility was unaffected. We next performed hepatic mRNA profiling with high-density microarrays. Male Sst-KO mice exhibited a globally feminized pattern of GH-dependent mRNA levels, but female Sst-KO mice were largely unaffected. Among the differentially expressed female-predominant genes was Serpina6, which encodes corticosteroid-binding globulin (CBG). Increased CBG was associated with elevated diurnal peak plasma corticosterone in unstressed WT females and both sexes of Sst-KO mice compared with WT males. Sst-KO mice also had exaggerated ACTH and corticosterone responses to acute restraint stress. However, consistent with their lack of phenotypic signs of excess glucocorticoids, cerebrospinal fluid concentrations of free corticosterone in Sst-KO mice were not elevated. In summary, SST is necessary for the prolonged interpulse troughs that define masculinized pituitary GH secretion. SST also contributes to sexual dimorphism of the hypothalamic-pituitary-adrenal axis via GH-dependent regulation of hepatic CBG production.


Subject(s)
Corticosterone/metabolism , Growth Hormone/metabolism , Somatostatin/metabolism , Transcortin/metabolism , Animals , Corticosterone/blood , Female , Growth Hormone/genetics , Male , Mice , Mice, Inbred C57BL , Mice, Knockout , RNA, Messenger/genetics , RNA, Messenger/metabolism , Sex Characteristics , Somatostatin/genetics , Transcortin/genetics
3.
Am J Physiol Endocrinol Metab ; 306(8): E904-15, 2014 Apr 15.
Article in English | MEDLINE | ID: mdl-24518677

ABSTRACT

Hypothalamic proopiomelanocortin (POMC) neurons constitute a critical anorexigenic node in the central nervous system (CNS) for maintaining energy balance. These neurons directly affect energy expenditure and feeding behavior by releasing bioactive neuropeptides but are also subject to signals directly related to nutritional state such as the adipokine leptin. To further investigate the interaction of diet and leptin on hypothalamic POMC peptide levels, we exposed 8- to 10-wk-old male POMC-Discosoma red fluorescent protein (DsRed) transgenic reporter mice to either 24-48 h (acute) or 2 wk (chronic) food restriction, high-fat diet (HFD), or leptin treatment. Using semiquantitative immunofluorescence and radioimmunoassays, we discovered that acute fasting and chronic food restriction decreased the levels of adrenocorticotropic hormone (ACTH), α-melanocyte-stimulating hormone (α-MSH), and ß-endorphin in the hypothalamus, together with decreased DsRed fluorescence, compared with control ad libitum-fed mice. Furthermore, acute but not chronic HFD or leptin administration selectively increased α-MSH levels in POMC fibers and increased DsRed fluorescence in POMC cell bodies. HFD and leptin treatments comparably increased circulating leptin levels at both time points, suggesting that transcription of Pomc and synthesis of POMC peptide products are not modified in direct relation to the concentration of plasma leptin. Our findings indicate that negative energy balance persistently downregulated POMC peptide levels, and this phenomenon may be partially explained by decreased leptin levels, since these changes were blocked in fasted mice treated with leptin. In contrast, sustained elevation of plasma leptin by HFD or hormone supplementation did not significantly alter POMC peptide levels, indicating that enhanced leptin signaling does not chronically increase Pomc transcription and peptide synthesis.


Subject(s)
Hypothalamus/metabolism , Leptin/metabolism , Nutritional Status/physiology , Pro-Opiomelanocortin/metabolism , Animals , Body Weight/drug effects , Diet , Eating/drug effects , Leptin/pharmacology , Male , Mice , Mice, Inbred C57BL , Mice, Transgenic , Pro-Opiomelanocortin/genetics , Time Factors
4.
J Clin Invest ; 122(11): 4203-12, 2012 Nov.
Article in English | MEDLINE | ID: mdl-23093774

ABSTRACT

Obesity is a chronic metabolic disorder affecting half a billion people worldwide. Major difficulties in managing obesity are the cessation of continued weight loss in patients after an initial period of responsiveness and rebound to pretreatment weight. It is conceivable that chronic weight gain unrelated to physiological needs induces an allostatic regulatory state that defends a supranormal adipose mass despite its maladaptive consequences. To challenge this hypothesis, we generated a reversible genetic mouse model of early-onset hyperphagia and severe obesity by selectively blocking the expression of the proopiomelanocortin gene (Pomc) in hypothalamic neurons. Eutopic reactivation of central POMC transmission at different stages of overweight progression normalized or greatly reduced food intake in these obesity-programmed mice. Hypothalamic Pomc rescue also attenuated comorbidities such as hyperglycemia, hyperinsulinemia, and hepatic steatosis and normalized locomotor activity. However, effectiveness of treatment to normalize body weight and adiposity declined progressively as the level of obesity at the time of Pomc induction increased. Thus, our study using a novel reversible monogenic obesity model reveals the critical importance of early intervention for the prevention of subsequent allostatic overload that auto-perpetuates obesity.


Subject(s)
Adipose Tissue/physiopathology , Adiposity , Eating , Hypothalamus/physiopathology , Obesity/prevention & control , Obesity/physiopathology , Adipose Tissue/metabolism , Adipose Tissue/pathology , Animals , Disease Models, Animal , Hyperphagia/genetics , Hyperphagia/metabolism , Hyperphagia/pathology , Hyperphagia/physiopathology , Hyperphagia/prevention & control , Hypothalamus/metabolism , Hypothalamus/pathology , Mice , Mice, Knockout , Neurons/metabolism , Neurons/pathology , Obesity/genetics , Obesity/metabolism , Pro-Opiomelanocortin/genetics , Pro-Opiomelanocortin/metabolism
5.
J Comp Neurol ; 518(15): 3130-48, 2010 Aug 01.
Article in English | MEDLINE | ID: mdl-20533364

ABSTRACT

Evidence showing expression of endogenous opioids in the mammalian retina is sparse. In the present study we examined a transgenic mouse line expressing an obligate dimerized form of Discosoma red fluorescent protein (DsRed) under the control of the pro-opiomelanocortin promoter and distal upstream regulatory elements to assess whether pro-opiomelanocortin peptide (POMC), and its opioid cleavage product, beta-endorphin, are expressed in the mouse retina. Using double label immunohistochemistry we found that DsRed fluorescence was restricted to a subset of GAD-67-positive cholinergic amacrine cells of both orthotopic and displaced subtypes. About 50% of cholinergic amacrine cells colocalized DsRed and a large fraction of DsRed-expressing amacrine cells was positive for beta-endorphin immunostaining, whereas beta-endorphin-immunoreactive neurons were absent in retinas of POMC null mice. Our findings contribute to a growing body of evidence demonstrating that opioid peptides are an integral component of vertebrate retinas, including those of mammals.


Subject(s)
Retina/metabolism , beta-Endorphin/biosynthesis , Adrenocorticotropic Hormone/metabolism , Amacrine Cells/metabolism , Animals , Antibody Specificity , Calbindin 2 , Calbindins , Choline O-Acetyltransferase/metabolism , Glutamate Decarboxylase/metabolism , Glycine Plasma Membrane Transport Proteins/metabolism , Immunohistochemistry , In Situ Hybridization , Luminescent Proteins , Mice , Mice, Inbred C57BL , Mice, Transgenic , Microscopy, Confocal , Parasympathetic Nervous System/metabolism , Pituitary Gland/metabolism , Pro-Opiomelanocortin/biosynthesis , Pro-Opiomelanocortin/genetics , S100 Calcium Binding Protein G/metabolism , alpha-MSH/metabolism , Red Fluorescent Protein
6.
J Neurosci ; 29(43): 13684-90, 2009 Oct 28.
Article in English | MEDLINE | ID: mdl-19864580

ABSTRACT

Proopiomelanocortin (POMC) neurons have been intensively studied because of their essential role in regulating energy balance and body weight. Many effects of POMC neurons can be attributed to their release of cognate neuropeptides from secretory granules in axon terminals. However, these neurons also synaptically release non-peptide neurotransmitters. The aim of this study was to settle the controversy whether there are separate populations of POMC neurons that release GABA or glutamate. Transgenic mice expressing a red fluorescent protein [Discosoma red (DsRed)] driven by Pomc neuronal regulatory elements (POMC-DsRed) were crossed to mice that expressed green fluorescent protein (gfp) in GABAergic neurons (GAD67-gfp). Approximately 40% of POMC neurons in the arcuate nucleus of the double-transgenic mice expressed the GAD67-gfp transgene. In vitro neurotransmitter release was detected using whole-cell electrophysiologic recordings in cultured GAD67-gfp-positive and GAD67-gfp-negative POMC neurons that had formed recurrent synapses (autapses). Autapses from GAD67-gfp-positive neurons were uniformly GABAergic. In contrast, autapses from the GAD67-gfp-negative POMC neurons exclusively exhibited postsynaptic currents mediated by glutamate. Together, these results indicate that there are two subpopulations of POMC neurons in the arcuate nucleus differentiated by their amino acid neurotransmitter phenotype. Whole-cell voltage-clamp recordings from POMC neurons in live brain slices indicated that GABAergic and glutamatergic POMC neurons are under similar presynaptic and postsynaptic regulation, although the GABAergic POMC neurons are smaller and have higher input resistance. GABAergic and glutamatergic POMC neurons may mediate distinct aspects of POMC neuron function, including the regulation of energy homeostasis.


Subject(s)
Arcuate Nucleus of Hypothalamus/physiology , Glutamic Acid/metabolism , Neurons/physiology , Pro-Opiomelanocortin/metabolism , gamma-Aminobutyric Acid/metabolism , Adrenocorticotropic Hormone/metabolism , Animals , Cells, Cultured , Female , Glutamate Decarboxylase/genetics , Glutamate Decarboxylase/metabolism , Green Fluorescent Proteins/genetics , Green Fluorescent Proteins/metabolism , In Vitro Techniques , Luminescent Proteins/genetics , Luminescent Proteins/metabolism , Male , Mice , Mice, Inbred C57BL , Mice, Transgenic , Patch-Clamp Techniques , Pro-Opiomelanocortin/genetics , Synapses/physiology , Red Fluorescent Protein
7.
Endocrinology ; 148(2): 647-59, 2007 Feb.
Article in English | MEDLINE | ID: mdl-17095588

ABSTRACT

Proopiomelanocortin (POMC) is synthesized predominantly in pituitary corticotrophs, melanotrophs, and arcuate hypothalamic neurons. Corticotroph-derived ACTH mediates basal and stress-induced glucocorticoid secretion, but it is uncertain whether POMC peptides produced in the brain also regulate the hypothalamic-pituitary-adrenal axis. To address this question, we generated neuron-specific POMC-deficient mice by transgenic (Tg) replacement of pituitary POMC in a global Pomc(-/-) background. Selective restoration of pituitary POMC prevented the adrenal insufficiency and neonatal mortality characteristic of Pomc(-/-) mice. However, adult Pomc(-/-)Tg/+ mice expressing the pituitary-specific transgene exhibited adrenal cortical hypertrophy, elevated basal plasma corticosterone, elevated basal but attenuated stress-induced ACTH secretion, and inappropriately elevated CRH expression in the hypothalamic paraventricular nucleus. In addition, Pomc(-/-)Tg/+, Pomc(+/-)Tg/+, and Pomc(+/-) mice, which all displayed varying degrees of elevated CRH, frequently developed melanotroph adenomas after 1 yr of age, whereas Pomc(-/-) mice, with maximal CRH expression and glucocorticoid disinhibition, developed corticotroph and melanotroph adenomas. These results indicate that neuronal POMC peptides are necessary to regulate CRH within physiological limits and that a chronic reduction or absence of hypothalamic POMC leads to trophic stimulation of pituitary cells directly or indirectly through elevated CRH levels.


Subject(s)
Brain/metabolism , Hypothalamo-Hypophyseal System/physiology , Pituitary-Adrenal System/physiology , Pro-Opiomelanocortin/physiology , Adenoma/etiology , Adenoma/pathology , Adrenal Cortex/pathology , Adrenal Insufficiency/etiology , Adrenal Insufficiency/mortality , Adrenocorticotropic Hormone/metabolism , Animals , Corticosterone/blood , Corticotropin-Releasing Hormone/metabolism , Female , Hypertrophy , Hypothalamo-Hypophyseal System/physiopathology , Hypothalamus/metabolism , Male , Melanotrophs/pathology , Mice , Mice, Knockout , Mice, Transgenic , Paraventricular Hypothalamic Nucleus/metabolism , Pituitary Gland/metabolism , Pituitary Neoplasms/etiology , Pituitary Neoplasms/pathology , Pituitary-Adrenal System/physiopathology , Pro-Opiomelanocortin/deficiency , Pro-Opiomelanocortin/genetics , Stress, Physiological/metabolism , Stress, Physiological/physiopathology
8.
J Neurosci ; 22(21): 9604-11, 2002 Nov 01.
Article in English | MEDLINE | ID: mdl-12417685

ABSTRACT

Stimulation of the dopamine (DA) system disrupts prepulse inhibition (PPI) of the acoustic startle response. On the basis of rat studies, it appeared that DA D2 receptors (D2Rs) rather than D1 receptors (D1Rs) regulate PPI, albeit possibly in synergism with D1Rs. To characterize the DA receptor modulation of PPI in another species, we tested DA D1R and D2R mutant mice with direct and indirect DA agonists and with the glutamate receptor antagonist, dizocilpine (MK-801). Neither the mixed D1/D2 agonist apomorphine (5 mg/kg) nor the more selective D1-like agonist SKF82958 (0.3 mg/kg) altered PPI in D1R knock-out mice, although both compounds disrupted PPI in D2R mutant and wild-type mice, suggesting that the D1R alone might modulate PPI in mice. However, amphetamine (10 mg/kg) significantly lowered PPI in each genotype of D1R mice, suggesting that the D1R is not necessary for the PPI-disruptive effect of the indirect agonist in mice. As reported previously, amphetamine (10 mg/kg) failed to disrupt PPI in D2R knock-out mice, supporting a unique role of the D2R in the modulation of PPI. Dizocilpine (0.3 mg/kg) induced similar PPI deficits in D1R and D2R mutant mice, confirming that the influences of the NMDA receptor on PPI are independent of D1Rs and D2Rs in rodents. Thus, both D1Rs and D2Rs modulate aspects of PPI in mice in a manner that differs from dopaminergic modulation in rats. These findings emphasize that further cross-species comparisons of the pharmacology of PPI are essential to understand the relevance of rodent PPI studies to the deficits in PPI observed in patients with schizophrenia.


Subject(s)
Dopamine Agonists/pharmacology , Neural Inhibition/drug effects , Receptors, Dopamine D1/agonists , Receptors, Dopamine D1/deficiency , Receptors, Dopamine D2/agonists , Receptors, Dopamine D2/deficiency , Amphetamine/pharmacology , Animals , Apomorphine/pharmacology , Behavior, Animal/drug effects , Behavior, Animal/physiology , Benzazepines/pharmacology , Dizocilpine Maleate/pharmacology , Electric Stimulation , Excitatory Amino Acid Antagonists/pharmacology , Female , Genotype , Heterozygote , Homozygote , Male , Mice , Mice, Inbred C57BL , Mice, Knockout , Neural Inhibition/physiology , Receptors, Dopamine D1/genetics , Receptors, Dopamine D2/genetics , Receptors, N-Methyl-D-Aspartate/antagonists & inhibitors , Reflex, Startle/drug effects , Reflex, Startle/genetics
9.
Mol Endocrinol ; 16(8): 1951-63, 2002 Aug.
Article in English | MEDLINE | ID: mdl-12145348

ABSTRACT

The peptide somatostatin (SST) is widely synthesized in the brain and periphery and acts through a family of five receptors (SSTR1-5) to exert numerous effects. A gene product related to SST, cortistatin (CST), also interacts with SSTR1-5. Here we have investigated the regulation of SSTR1-5 and of CST in SST knockout (SSTKO) mice. The five SSTRs were quantitated individually by subtype-selective binding analysis, by immunocytochemistry, and by mRNA measurement and showed, in the brain of SSTKO mice, up-regulation of subtypes 1, 2, 4, and 5, and down-regulation of SSTR3. Peripheral tissues displayed both subtype- and tissue-specific changes in SSTR1-5 mRNA levels of expression. Lack of SST did not up-regulate normal CST expression in brain nor did it induce its expression in the periphery. SST-like immunoreactivity, however, was induced in the proximal midgut in SSTKO animals, suggesting intestinal expression of a novel SST-like gene.


Subject(s)
Brain/metabolism , Receptors, Somatostatin/genetics , Receptors, Somatostatin/metabolism , Somatostatin/deficiency , Animals , Immunohistochemistry , Intestinal Mucosa/metabolism , Membrane Proteins , Mice , Mice, Inbred C57BL , Mice, Knockout , Neuropeptides/genetics , Neuropeptides/metabolism , RNA, Messenger/genetics , RNA, Messenger/metabolism , Receptors, Somatostatin/classification , Somatostatin/genetics , Tissue Distribution , Up-Regulation
10.
Mol Cell Endocrinol ; 189(1-2): 97-103, 2002 Mar 28.
Article in English | MEDLINE | ID: mdl-12039068

ABSTRACT

Ghrelin activates GH release and is implicated in growth and metabolic regulation. The regulation of its biosynthesis has not been well studied. The current investigation was designed to examine some of the factors that may influence ghrelin gene expression in the stomach. Thus, in C57BL/6 mice, ghrelin mRNA was detectable by Northern blots throughout the age groups studied, but the levels changed markedly over time. Levels were low at E18.5 and increased rapidly after birth to 6-fold at P14 before peaking to 8-fold at P21. The levels then exhibited a gradual decline at P60 (75% of the peak level) and at 6 months (67%) and a drastic decrease as the animals aged to 19 months (only 5%). Furthermore, sexual dimorphic gene expression, the effect of liver-derived IGF-I deficiency, as well as ghrelin secretion were studied. Our results support a role of ghrelin in growth/metabolism in juvenile and young adult mice of both sexes and in sexually dimorphic regulation of GH secretion in aged mice.


Subject(s)
Gene Expression Regulation , Insulin-Like Growth Factor I/metabolism , Peptide Hormones/metabolism , Sex Characteristics , Age Factors , Animals , Cyclophilins/genetics , Cyclophilins/metabolism , Female , Ghrelin , Growth Hormone/genetics , Growth Hormone/metabolism , Insulin-Like Growth Factor I/genetics , Liver/metabolism , Male , Mice , Mice, Inbred C57BL , Peptide Hormones/genetics , Pregnancy , Stomach/physiology
11.
Endocrinology ; 143(7): 2599-609, 2002 Jul.
Article in English | MEDLINE | ID: mdl-12072392

ABSTRACT

Preprosomatostatin is a gene expressed ubiquitously among vertebrates, and at least two duplications of this gene have occurred during evolution. Somatostatin-28 (S-28) and somatostatin-14 (S-14), C-terminal products of prosomatostatin (ProS), are differentially expressed in mammalian neurons, D cells, and enterocytes. One pathway for the generation of S-14 entails the excision of Arg13-Lys14 in S-28, leading to equivalent amounts of S-28((1-12)). Using an antiserum (F-4), directed to the N-terminal region of S-28 that does not react with S-28((1-12)), we detected a peptide, in addition to S-28 and ProS, that was present in human plasma and in the intestinal tract of rats and monkeys. This F-4 reacting peptide was purified from monkey ileum; and its amino acid sequence, molecular mass, and chromatographic characteristics conformed to those of S-28((1-13)), a peptide not described heretofore. When extracts of the small intestine were measured by RIA, there was a discordance in the ratio of peptides reacting with F-4 and those containing the C terminus of ProS, suggesting sites of synthesis for S-28((1-13)) distinct from those for S-14 and S-28. This was supported by immunocytochemistry, wherein F-4 reactivity was localized in gastrointestinal (GI) endocrine cells and a widespread plexus of neurons within the wall of the distal gut while immunoreactivity to C-terminal domains of S-14 and S-28 in these neurons was absent. Further, F-4 immunoreactivity persisted in similar GI endocrine cells and myenteric neurons in mice with a targeted deletion of the preprosomatostatin gene. We believe that these data suggest a novel peptide produced in the mammalian gut, homologous with the 13 residues of the proximal region of S-28 but not derived from the ProS gene. Pending characterization of the gene from which this peptide is derived, its distribution, and function, we have designated this peptide as thrittene. Its localization in both GI endocrine cells and gut neurons suggests that thrittene may function as both a hormone and neurotransmitter.


Subject(s)
Digestive System/metabolism , Peptide Fragments/physiology , Somatostatin/physiology , Adult , Animals , Chromatography, Affinity , Chromatography, Gel , Chromatography, High Pressure Liquid , Humans , Immunohistochemistry , Macaca mulatta , Male , Mice , Mice, Inbred C57BL , Mice, Knockout , Middle Aged , Peptide Fragments/genetics , Peptide Fragments/metabolism , Protein Precursors/biosynthesis , Protein Precursors/genetics , Radioimmunoassay , Rats , Rats, Wistar , Somatostatin/biosynthesis , Somatostatin/genetics , Somatostatin/metabolism , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
12.
Epilepsy Res ; 48(1-2): 43-56, 2002 Jan.
Article in English | MEDLINE | ID: mdl-11823109

ABSTRACT

Patients and experimental models of temporal lobe epilepsy display loss of somatostatinergic neurons in the dentate gyrus. To determine if loss of the peptide somatostatin contributes to epileptic seizures we examined kainate-evoked seizures and kindling in somatostatin knockout mice. Somatostatin knockout mice were not observed to experience spontaneous seizures. Timm staining, acetylcholinesterase histochemistry, and immunocytochemistry for NPY, calbindin, calretinin, and parvalbumin revealed no compensatory changes or developmental abnormalities in the dentate gyrus of somatostatin knockout mice. Optical fractionator counting of Nissl-stained hilar neurons showed similar numbers of neurons in wild type and somatostatin knockout mice. Mice were treated systemically with kainic acid to evoke limbic seizures. Somatostatin knockout mice tended to have a shorter average latency to stage 5 seizures, their average maximal behavioral seizure score was higher, and they tended to be more likely to die than controls. In response to kindling by daily electrical stimulation of the perforant path, to more specifically challenge the dentate gyrus, mean afterdischarge duration in somatostatin knockout mice was slightly longer, but the number of treatments to five stage 4-5 seizures was similar to controls. Although we cannot exclude the possibility of undetected compensatory mechanisms in somatostatin knockout mice, these findings suggest that somatostatin may be mildly anticonvulsant, but its loss alone is unlikely to account for seizures in temporal lobe epilepsy.


Subject(s)
Seizures/genetics , Seizures/physiopathology , Somatostatin/deficiency , Somatostatin/genetics , Animals , Dentate Gyrus/anatomy & histology , Dentate Gyrus/metabolism , Electric Stimulation/methods , Hippocampus/chemistry , Hippocampus/metabolism , Hippocampus/physiology , Kindling, Neurologic/genetics , Kindling, Neurologic/metabolism , Male , Mice , Mice, Inbred C57BL , Mice, Knockout , Neurons/chemistry , Neurons/metabolism , Neurons/physiology , Seizures/chemically induced , Severity of Illness Index
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