离断大鼠迷走神经肝支对血糖血脂水平的影响及其与mTOR表达水平的关系

目的　探讨离断大鼠迷走神经肝支对血糖、血脂水平的影响及其与mTOR表达水平的关系,为糖脂代谢神经调节机制研究提供实验依据。 方法　建立离断迷走神经肝支大鼠模型作为实验组,另设迷走神经肝支探查的假手术组和不作任何处理的对照组,术后每两周检测大鼠血糖、血脂、胰岛素和皮质醇水平、肝和骨骼肌组织的糖原含量以及mTOR的表达水平。 结果　实验组大鼠与对照组大鼠相比,术后2周胰岛素水平升高、肝糖原含量增多、血糖水平降低（P<0.05）;术后6周,肝、骨骼肌组织mTOR表达增多、肝糖原及骨骼肌糖原含量降低、血糖水平增高、甘油三酯水平增高,高密度脂蛋白水平降低（P<0.05）。假手术组和对照组大鼠各项指标各时间点无明显差异（P>0.05）。 结论　离断大鼠迷走神经肝支可导致糖脂代谢以及糖原含量异常,其机制可能与胰岛素水平变化以及肝、骨骼肌mTOR表达水平升高有关。     

离断大鼠迷走神经肝支对血糖血脂水平的影响及其与mTOR表达水平的关系

目的　探讨离断大鼠迷走神经肝支对血糖、血脂水平的影响及其与mTOR表达水平的关系,为糖脂代谢神经调节机制研究提供实验依据。 方法　建立离断迷走神经肝支大鼠模型作为实验组,另设迷走神经肝支探查的假手术组和不作任何处理的对照组,术后每两周检测大鼠血糖、血脂、胰岛素和皮质醇水平、肝和骨骼肌组织的糖原含量以及mTOR的表达水平。 结果　实验组大鼠与对照组大鼠相比,术后2周胰岛素水平升高、肝糖原含量增多、血糖水平降低（P<0.05）;术后6周,肝、骨骼肌组织mTOR表达增多、肝糖原及骨骼肌糖原含量降低、血糖水平增高、甘油三酯水平增高,高密度脂蛋白水平降低（P<0.05）。假手术组和对照组大鼠各项指标各时间点无明显差异（P>0.05）。 结论　离断大鼠迷走神经肝支可导致糖脂代谢以及糖原含量异常,其机制可能与胰岛素水平变化以及肝、骨骼肌mTOR表达水平升高有关。     

Effect of lysine on afferent activity of the hepatic branch of the vagus nerve in normal and L-lysine-deficient rats

Amino acid deficiency was modeled by feeding rats a diet deficient in the essential L-amino acid, L-lysine (L-lys). There is a rapid anorectic response to such a diet, and a strong preference for L-lys develops during the deficiency. While the brain appears to trigger this preference, the peripheral pathways that inform the brain about the deficiency are not well understood. One possible information pathway may utilize an "amino acid sensor" in the hepatoportal region. In the present study, we measured in vivo neural activity in normal and L-lys-deficient rat. Compared to the normally fed controls, we found an approximately 100-fold increase in the firing sensitivity of the L-lys sensors in vagal afferent fibers from the hepatoportal region of the L-lys-deficient rats. Injection of 10 mM L-lys into the hepatoportal circulation, but not D-lysine (D-lys), evoked an increase in afferent activity. While L-lys deficiency enhanced the sensitivity of the L-lys sensors, the sensitivity due to other small amino acid sensors remained unchanged. Finally, we observed a time-dependent response of the lysine sensors to lysine deficiency. It required 3-4 days of maintenance on the lysine-deficient diet for the sensitivity of the L-lys sensors to change. Taken together, these results provide additional data to support the existence of putative L-amino acid sensors in the hepatoportal circulation. Additionally, they describe several characteristics of the L-lys sensors and show that these sensors may contribute to the adaptation to dietary L-lys deficiency and to maintenance of L-amino acid homeostasis.     

Effect of chronic acamprosate treatment on voluntary alcohol intake and beta-endorphin plasma levels in rats selectively bred for high alcohol preference

Our previous studies have shown that repeated acamprosate administration to ethanol-naive Warsaw high preferring (WHP) rats resulted in increased plasma beta-endorphin levels and at least partially prevents increases in levels of this peptide after a single administration of ethanol compared with untreated control rats. The objective of the present study, which included 45 WHP rats, was to continue the past research and investigate the effect of 10-day acamprosate treatment (200 mg/kg p.o.) on alcohol intake using a free-choice procedure and on changes in plasma beta-endorphin levels while alcohol is available, and 10 days after alcohol withdrawal. Voluntary alcohol consumption increases plasma levels of beta-endorphin from 440+/-25 pg/ml to 711+/-57 pg/ml (p=0.0002). After a 10-day of alcohol withdrawal, the levels of this peptide were significantly reduced compared with levels in rats with free access to ethanol (711+/-57 pg/ml vs. 294+/-38 pg/ml, p=0.000001) and in control naive rats (440+/-25pg/ml vs. 294+/-38pg/ml, p=0.044). Chronic treatment with acamprosate increased plasma beta-endorphin levels both in WHP rats with free access to ethanol (440+/-25 pg/ml vs. 616+/-49 pg/ml, p=0.008) and in rats after ethanol withdrawal (440+/-25 pg/ml vs. 620+/-56 pg/ml, p=0.007). In the group with free access to ethanol, there was a significant reduction in mean ethanol intake, from 6.75+/-0.20 g/kg body weight/day to 4.68+/-0.25 g/kg/day. Our results indicate that chronic acamprosate treatment may have beneficial effects, as it increases the beta-endorphin concentration thereby compensating for beta-endorphin deficiency during ethanol withdrawal. As the endogenous opioid system has an important role in the development of craving for alcohol, restoring the alcohol-induced deficits in beta-endorphin levels may be an important factor to prevent craving and maintaining abstinence. We suppose that the anti-craving mechanism of acamprosate that has been reported to abolish excessive glutamate release during alcohol withdrawal may be accompanied by compensation for the beta-endorphin deficiency.     

Angiotensin II stimulates water and NaCl intake through separate cell signalling pathways in rats

Angiotensin II (AngII) stimulation of water and NaCl intake is a classic model of the behavioural effects of hormones. In vitro studies indicate that the AngII type 1 (AT₁) receptor stimulates intracellular pathways that include protein kinase C (PKC) and mitogen-activated protein (MAP) kinase activation. Previous studies support the hypotheses that PKC is involved in AngII-induced water, but not NaCl intake and that MAP kinase plays a role in NaCl consumption, but not water intake, after injection of AngII. The present experiments test these hypotheses in rats using central injections of AngII in the presence or absence of a PKC inhibitor or a MAP kinase inhibitor. Pretreatment with the PKC inhibitor chelerythrine attenuated AngII-induced water intake, but NaCl intake was unaffected. In contrast, pretreatment with U0126, a MAP kinase inhibitor, had no effect on AngII-induced water intake, but attenuated NaCl intake. These data support the working hypotheses and significantly extend our earlier findings and those of others. Perhaps more importantly, these experiments demonstrate the remarkable diversity of peptide receptor systems and add support for the surprising finding that intracellular signalling pathways can have divergent behavioural relevance.     

Diurnal patterns of food intake and plasma corticosterone levels in lactating rats

The diurnal patterns of food intake and plasma corticosterone levels were determined in lactating Wistar-Imamichi rats maintained in a light (14 L: 10 D, lights on 0500 hr) and temperature (24±2°C) controlled animal room. Lactating mothers with four or more than eight pups showed a characteristic diurnal pattern of food intake with high rates of intake around the time of lights off. The diurnal rhythmicity of food intake seemed to disappear in late lactation in mothers with more than eight pups. The plasma corticosterone concentration on day 9 of lactation displayed a diurnal rhythm with high values at 1700 hr and 2100 hr. The rhythmicity of the corticosterone levels was abolished on day 16 of lactation and a high level was maintained throughout a 24 hr period. Since the diurnal rhythm of the corticosterone level was shifted in animals fed during the restricted period (0900–1700 hr) from days 2 to 9 of lactation, the appearance of diurnal rhythm of corticoid secretion seemed to depend on the diurnal feeding rhythm in lactation as well as in the estrous cycle.     

Effect of protein intake on weight gain and plasma amino acid levels in uremic rats.

Chronically uremic rats weighing approximately 180-200 g and sham-operated controls of similar weight were pair fed diets containing 5, 15 or 23% protein for 10-12 wk. At each level of protein intake, uremic animals gained less weight and had lower protein efficiency ratios than controls. In addition, certain plasma amino acid levels were altered in the uremic animals. These included tyrosine and the tyrosine/phenylalanine ratio, which were decreased, and citrulline, glycine, and the methylhistidines, which were increased. In both uremic and control rats, plasma concentrations of certain amino acids, primarily nonessential ones, varied inversely with protein intake; with the 5% protein diet, the ratio of essential to nonessential amino acids was significantly reduced. These observations indicate that both uremia and reduced protein intake may affect growth and amino acid metabolism in rats with chronic renal failure. The finding that uremic rats utilize protein less efficiently may indicate that marked reductions in protein intake may be particularly hazardous to the nutritional status of the uremic patient.     

MSG intake suppresses weight gain, fat deposition, and plasma leptin levels in male Sprague-Dawley rats

Monosodium l-glutamate (MSG), an umami taste substance, may be a key molecule coupled to a food intake signaling pathway, possibly mediated through a specific l-glutamate (GLU) sensing mechanism in the gastrointestinal tract. Here we investigated the effect of the spontaneous ingestion of a 1% MSG solution and water on food intake and body weight in male Sprague-Dawley rats fed diets of varying caloric density, fat and carbohydrate contents. Fat mass and lean mass in the abdomen, blood pressure, and several blood metabolic markers were also measured. Rats given free access to MSG and water showed a high preference (93-97%) for the MSG solution, regardless of the diet they consumed. Rats ingesting MSG had a significantly smaller weight gain, reduced abdominal fat mass, and lower plasma leptin levels, compared to rats ingesting water alone. Naso-anal length, lean mass, food and energy intakes, blood pressure, blood glucose, and plasma levels of insulin, triglyceride, total cholesterol, albumin, and GLU were not influenced by the ingestion of the MSG solution. These same effects were observed in a study of adult rats. Together, these results suggest that MSG ingestion reduces weight gain, body fat mass, and plasma leptin levels. Moreover, these changes are likely to be mediated by increased energy expenditure, not reduced energy intake or delayed development. Conceivably, these effects of MSG might be mediated via gut GLU receptors functionally linked to afferent branches of the vagus nerve in the gut, or the afferent sensory nerves in the oral cavity.     

Single opioid administration modifies gonadal steroids in both the CNS and plasma of male rats

While morphine remains one of the most widely used opioids for the treatment of painful conditions, other opioids are also commonly employed. Because of the interactions between opioids and gonadal hormones, in particular opioid-induced hypogonadism, this study investigated the effects of widely used opioids on plasma testosterone and estradiol levels and brain testosterone levels in male rats. Animals were s.c. injected with two concentrations of morphine (5 or 10 mg/kg), fentanyl (0.05 or 0.1 mg/kg), tramadol (10 or 40 mg/kg), buprenorphine (0.05 or 0.1 mg/kg) or saline (0.7 ml/kg). Four or 24 h after treatment, the rats were deeply anesthetized to collect blood samples from the abdominal aorta and to perfuse the brains with saline. Plasma and brain hormone levels were measured by radioimmunoassay. In rats studied 4 h after treatment, all the opioids except tramadol 10 mg/kg decreased plasma testosterone in comparison with saline administration. At the same time, plasma estradiol levels were lower than control in the groups treated with the low doses of morphine, tramadol and buprenorphine, while estradiol remained at control levels in the other groups. Twenty-four hours after treatment, plasma testosterone levels were different (higher) than control in the animals treated with the low doses of morphine, fentanyl and buprenorphine. Estradiol was lower than control in the low dose groups, while the high doses did not produce any changes with respect to control. Four hours after treatment, brain testosterone was drastically decreased in all groups except buprenorphine, in which it remained at control levels. All groups returned to control levels at 24 h after treatment. In conclusion, opioids exert important effects on plasma and CNS sex hormone levels. The different magnitude and time-course of the effects of the different opiates on testosterone and estradiol levels are likely due to their different mechanism of action.     

The effect of endogenous sugar acids on the afferent discharge rate of the hepatic branch of the vagus nerve in the rat

The effects of intraportal administration of endogenous sugar acids such as 2DTA, 3DPA and 2B40 on afferent activity of the hepatic branch of the vagus nerve were investigated in the rat. A decrease in afferent discharge rate was observed after administration of 2DTA (0.1 mM approximately 10 mM, 0.1 ml) and 2B4O (100 nM approximately 2 microM, 0.1 approximately 0.2 ml), whereas 3DPA (0.1 mM approximately 10 mM, 0.1 ml) increased the afferent activity. These observations suggest that 2DTA and 2B4O suppress, and 3DPA enhances food intake behavior and may be important in the regulation of blood glucose homeostasis through glucose-sensitive vagal hepatic afferent fibers.     

Suppression of food intake in diabetic rats by voluntary consumption and intrahypothalamic injection of glucose

When given a choice between 2 concentrations of glucose (5 and 35%) normal rats prefer to consume most of their glucose from the concentrated source while diabetics prefer the dilute source. Although both consume approximately the same total amount of glucose, on a caloric basis the glucose depressed chow intake more in diabetics than in normal rats, indicating that diabetics can experience the satiating effects of glucose. Also, since the diabetics excreted more glucose in urine during the glucose access, the overall retention of calories appeared to be less than of controls, indicating the diabetics are effectively hypophagic as compared to controls when they ingested large quantities of glucose. Direct injection of glucose into the ventromedial hypothalamus suppressed feeding as effectively in diabetics as in controls, indicating that normal titers of insulin are probably not necessary for suppression of feeding by ingested glucose in diabetic animals.     

The effect of electrical stimulation of the hepatic branch of the vagus nerve on the secretion of gastric acid in the rat.

Electrical stimulation of the hepatic vagus nerve brought a transient increase in acid concentration in a perfusate collected from the stomach. These observations suggest that there might be a neural system which modulates the secretion of gastric acid through hepatic vagal afferents and gastric vagal efferents.     

Changes in monoamines and their metabolite levels in substantia nigra of aged rats

A decrease in the monoamine and monoamine metabolite contents in the substantia nigra of aged rats vs. controls has been found. Hence, it can be speculated that this decrease may play a role in the multiple alterations in dopaminergic functions observed in aged rats.     

The effect of gestational ethanol exposure on voluntary ethanol intake in early postnatal and adult rats

Clinical and epidemiological studies provide strong data for a relationship between prenatal ethanol exposure and the risk for abuse in adolescent and young adult humans. However, drug-acceptance results in response to fetal exposure have differed by study, age at evaluation, and experimental animal. In the present study, the authors tested whether voluntary ethanol intake was enhanced in both the infantile and adult rat (15 and 90 days of age, respectively), as a consequence of chronic fetal drug experience. Experimental rats were exposed in utero by administering ethanol to a pregnant dam in a liquid diet during gestational Days 6-20. Compared with those for isocaloric pair-fed and ad lib chow control animals, the results for experimental animals demonstrated that fetal exposure significantly increased infantile affinity for ethanol ingestion without affecting intake patterns of an alternative fluid (water). Heightened affinity for ethanol was absent in adulthood. Moreover, the results argue against malnutrition as a principal factor underlying the infantile phenomenon. These data add to a growing literature indicative of heightened early postnatal acceptance patterns resulting from maternal use or abuse of ethanol during pregnancy.     

Changes in monoamines and their metabolite levels in some brain regions of aged rats

The concentrations of dopamine (DA) norepinephrine (NE), serotonin (5HT) and their metabolites, HVA, DOPAC, MHPG-SO4 and 5HIAA were measured in several brain areas of rats aged 4, 18 and 29 months. Dopamine and its metabolites showed a decline, statistically correlated with age, in all the dopaminergic areas considered, indicating that this system is profoundly affected in the senescent rat. The changes in the noradrenergic system were more complex. This neurotransmitter was reduced in spinal cord and in limbic area, but was not modified in hippocampus, cerebellum, striatum and s. nigra. In cortex, MHPG-SO4, the main NE metabolite, showed a significantly age-related increase. Tyrosine hydroxylase (TH) activity was low in striatum, and brainstem but not in hypothalamus of aged rats. Neither 5HT nor its metabolites was affected by age. The results indicate that central catecholaminergic systems are markedly affected in senescent rats.     

Effects of dietary cholesterol and voluntary exercise on histopathology,plasma and hepatic lipids of the male rat

Summary To avoid the stress of imposed activity, male weanling rats were allowed to exercise voluntarily in individual activity wheels. The exercising animals, which were compared to sedentary controls, ran over 26 km/wk (over 2 miles/day). Half of the animals in each group were fed a 10% coconut oil diet; the other half were fed the same diet with 1% added cholesterol.Plasma cholesterol was monitored throughout the 23-week regime. Consistently lower plasma cholesterol values were shown by the exercising animals during the first weeks of the study, the differences being statistically significant at the end of the 8th week. Dietary cholesterol sharply elevated plasma cholesterol, which reached a peak at the 5th week, then declined to basal levels by the 10th week.Both neutral glycerides and cholesterol levels of the livers were elevated considerably by the addition of cholesterol to the diet. Exercising, however, had a lowering effect on both liver cholesterol and neutral glycerides. The weights of the hearts of the exercising rats were increased, while those of the other organs selected were unchanged.Histologic examination of sections of livers showed fat infiltration of hepatic cells varying in severity, depending on the diet. Greater damage to liver cells was noted when cholesterol was added to the basal diet. Fat infiltration was lessened considerably in exercising rats on the basal diet; exercising partially overcame the effects of added cholesterol.This work was supported in part by Grant-In-Aid from The Nutrition Foundation, Inc.; State of Washington Initiative 171 Fund and USPHS Research Grant HD-03475 from the National Institutes of Health.     

Relationship between the concentration of cholecystokinin-like immunoreactivity in plasma and food intake in male rats

In food-deprived male rats IP injection of cholecystokinin octapeptide (CCK-8, 5 micrograms), ingestion of food or ejaculation caused a comparable increase in plasma concentrations of CCK-8 and inhibited food intake. IV injection of 0.1 microgram CCK-8 interrupted ongoing feeding and greatly increased plasma CCK-8 levels. Osmotic minipumps delivering 0.5 micrograms CCK-8/h implanted IP reduced meal size and caused a modest increase in plasma CCK-8 levels. Injection of 5 micrograms CCK-8 IP produced an abrupt but transient increase in plasma CCK-8 concentrations whereas plasma concentrations of CCK-8 increased gradually with feeding. Injection of 5 micrograms CCK-8 IP, but not feeding, caused a marked increase in plasma oxytocin levels. The suppression of feeding, but not the increase in oxytocin, induced by IP CCK-8 was reversed by ICV injection of the CCK antagonist proglumide in a dose (100 micrograms) which failed to affect food intake if injected IP. Deprivation of food decreased and feeding increased the concentration of CCK-like immunoreactivity in the CSF. It is suggested that CCK-8 inhibits feeding in physiological doses by a specific mechanism in which peripheral as well as central neural CCK is involved.     

Afferent nerve endings in the tracheal muscle of guinea-pigs and rats

Summary The trachea of guinea-pigs was stained as a whole-mount preparation with the zinc iodide-osmium technique. A distinct class of nerve endings was observed associated with the tracheal muscle. The endings, issued from myelinated fibres of the vagus nerve via the recurrent laryngeal nerve, are distributed on either side of the midline and ventral to the tips of cartilages. They are interpreted as afferent nerve endings that may correspond to slow adapting stretch receptors identified by physiological studies. Each nerve contributes predominantly, but not exclusively, to the receptors of the ipsilateral side. There are 120–180 receptors along the full length of the guinea-pig trachea, their density being higher at the cranial end. The receptors are variable in size and structural complexity, and, to some extent, also in spatial orientation, but distinct subtypes are not recognizable. Receptors of similar morphology and distribution are found also in the rat trachea. The receptors can also be visualized with a cytochrome oxidase method for nerve endings, but they do not stain with immunohistochemistry for the neuropeptides substance P, calcitonin gene-related peptide, vasointestinal polypeptide and neurotensin.     

The role of adrenal or testicular hormones in voluntary ethanol and NaCl intake of crowded and individually housed rats

The effect of adrenalectomy or castration on the ingestive behaviour of 10% ethanol, 0.5 M NaCl, water, and food was investigated in 2 models of increased/high ethanol consumption (1) adult male rats, previously individually housed with low ethanol intake, moved crowded housing and (2) individually housed adult male rats with high ethanol intake in the absence of any known aetiology. In study 1, rats that had been previously individually housed were paired with an animal in a small cage with ad libitum access to 10% ethanol intake, 0.5 M NaCl, water, and food at all times. Rats significantly increased 10% ethanol intake after they were pair-housed. The pairs were either adrenalectomized, castrated or sham operated. Neither adrenalectomy nor castration resulted in a significant change in 10% ethanol intake. 0.5 M NaCl intake was elevated and food intake and body weight were decreased in adrenalectomized rats. In study 2, rats that consumed large amounts of ethanol in the absence of any known aetiology remained in individual housing. Ethanol intake was decreased subsequent to either adrenalectomy or castration; adrenalectomy resulted in an increase in 0.5 M NaCl intake. These results suggest that the influence of adrenal or testicular hormones on ethanol intake is situation dependent. The increase in ethanol intake induced by placing animals in crowded housing appears to be independent of these hormones.