Printer Friendly

Effect of permanent hypoinsulinemia on appetite, performance, carcass composition, blood metabolites and leptin concentrations in lambs.

INTRODUCTION

Appetite is one of the most important aspects of energy homeostasis that is influenced by a variety of internal and external factors. On the basis of the kind of effect, internal factors are divided into two major series of signals; orexigenic signals, such as neuropeptide Y (NPY), agouti gene-related peptide (AgRP), ghrelin and orexin, that stimulate appetite, while anorexigenic signals, such as insulin, leptin, Pro-opiomelanocortin, inhibit appetite and consequently the resultant interaction determines appetite (Schwartz et al., 2000; Gerozissis, 2004; Broberger, 2005).

Insulin and leptin are two potent anorexigenic signals that agonistically suppress appetite. In the periphery, both of them are secreted in proportion to body fat mass (Niswender et al., 2004; Shan et al., 2008) and enter into the brain as adiposity signals (Woods and Porte, 1977; Niswender et al., 2004). In the brain, especially in the arcuate nucleus of the hypothalamus, they exert their effects by interacting with two opposing sets of neurons; NPY/AgRP neurons that are suppressed (Schwartz et al., 1992; Sipols et al., 1995; Sorensen et al., 2002), and other, POMC neurons that are stimulated by them (Benoit et al., 2002; Sorensen et al., 2002; Breen et al., 2005).

Insulin is mainly known for its putative glucoregulatory roles as an anabolic hormone while in the center, it exerts a catabolic effect by reducing appetite that was shown in some species (Woods et al., 1979; Foster et al., 1991; Air et al., 2002). On the other hand, insulin acts as a potent secretagogue of leptin from adipocytes (Barr et al., 1997; Patel et al., 1998). Therefore, their circulating levels are positively correlated.

Hypoinsulinemia is a useful situation for investigating the roles of insulin and also some related hormones, especially leptin, in control of appetite and growth parameters. In this situation, peripheral anabolic and also central catabolic effects of insulin and leptin are more clearly observed. These effects have been frequently studied in rodents but few studies have been carried out in ruminants, despite prominent differences in neuroendocrine pathways, metabolic fuels (Bergman, 1990; Gabel and Sehested, 1997), feeding patterns and insulin sensitivity (Prior and Smith, 1983; Sasaki and Takahashi, 1983; Sano et al., 1985) between ruminants and rodents. Thus, in this study we induced hypoinsulinemia using streptozotocin in growing lambs to investigate changes in appetite, growth parameters, carcass composition and other related blood metabolites.

MATERIALS AND METHODS

Animals

Twenty male Zel lambs (three months-old) weighing 19.4 [+ or -] 1.6 kg were assigned to the experiment and identified with ear plaques (Shirang research station of Zel breed, Gorgan, Iran). All animals were maintained in a common pen and fed the same ration. Two weeks prior to the beginning of the experiment, animals were randomly divided into four treatment groups and housed in individual, sheltered pens (2.25 m2) under ambient temperature and photoperiod. Animals were fed ad libitum with a mixture of alfalfa hay (60% of DMI) and concentrate (40% of DMI) in the form of a total mixed ration containing 2.6 Mcal of ME and 14% CP per kg DM to meet their requirements (NRC, 1985). Mineral blocks and water were available at all times.

After two weeks of adaptation to experimental conditions and ration, the main stage of the experiment was initiated involving eight consecutive weeks- three weeks considered as pre-injection interval and the following five weeks as post-injection interval. At the end of the third week, STZ was injected intravenously and then animals entered the post-injection interval.

Hypoinsulinemia induction

Hypoinsulinemia was induced by single intravenous injection of STZ (Sigma Chemical Co., St. Louis, MO, USA) as previously described (Higdon et al., 2001; Ramanathan et al., 2004). Briefly, STZ was dissolved in citrate buffer (pH = 4.5) in three final concentrations and then, fresh solutions were immediately injected via the jugular vein using sterile syringes within five minutes after preparation. The treatments were single injection of four doses of STZ; 0, 25, 50 and 75 mg/kg BW and named C, L, M and H, respectively. Control group (C) received buffer solution alone.

Forty eight hours after STZ injection, animals in treatment H showed severe diabetic symptoms, such as cachexia, hypophagia and polyurea, and therefore needed insulin therapy and electrolyte therapy for survival. Indeed, they posed such abnormal conditions that they could not continue the experiment. Insulin therapy produced data not suitable for assays of hormones and other metabolites. Thus, the experiment continued with C, L and M treatment groups.

Data collection

During each week, daily feed and water intakes (WI) were measured on a specific day and extended to all days of the respective week. Hence, feed and water were weighed and offered ad libitum to animals twice daily at 8:00 and 14:00 and that remaining was assessed at 07:00 to 08:00 of the next day when animals avoided eating or drinking and were recumbent. These data were calculated as g feed or water offered to each animal minus g of remaining. Animals were weighed weekly at 07:00 before morning feeding and their weekly weight gain was recorded. Feed conversion ratio (FCR) was calculated individually by dividing feed intake into weight gain.

Blood samples were collected twice on a specific day of each week via jugular venipuncture using ice-cooled sterile vacuum tubes (Pars Khavar Co., Qazvin, Iran); once when animals were fasted and the second at 2.5 h after feeding (post-prandial). These days were discrete from those on which feed intake was measured because of the stress that blood collection causes on feeding behavior of animals. Samples were immediately centrifuged at 3,500 RPM for 15 min. Sera were harvested and stored in sterile tubes, then frozen at -25[degrees]C until measurements were made.

All blood metabolites were measured by spectrophotometric methods (Thomas, 1998). Briefly, glucose concentrations were measured via glucose oxidase method, triglycerides via glycerol-3-phosphate method, cholesterol via cholesterol oxidase method, blood urea nitrogen (BUN) via bertholet method, albumin via bromocresol green method, ketone bodies (KB) via nitroproside strip, (all with commercial, diagnostic kits of Pars Azmun Co., Tehran, Iran) and total protein (TP) was measured via modified biuret method (with diagnostic kit of Zistchem Co., Tehran, Iran).

Serum insulin and leptin were measured via radioimmunoassay (RIA) kits (TYN Co., No. 212, Gupre St. Bruxele, Belgium) based on a double antibody RIA method with antisera raised against ovine insulin and leptin. Intra- and inter-assay coefficients of variation were, respectively, less than 5% and 9% for insulin and less than 5% and 6% for leptin.

At the end of the experiment, animals were killed to determine empty body weight (EBW) and carcass composition. The fillet of vertebra 12 and the cranial lobe of liver were removed and analyzed to determine DM, CP and crude fat contents. Urine samples were collected directly from the bladder and used for urinalysis. All the experiments were approved by the animal care committee of Gorgan University of Agricultural Sciences and Natural Resources.

Statistical analyses

Data measured over weeks were analyzed as a repeated measures design using the mixed model procedure of SAS software (SAS, 1996).The tested effects were treatment (citrate buffer vs. STZ), week (time) and two-way interaction (treatment x week). The main effect of treatment was tested using animal within treatment as the error term and the residual error was used to test week and interaction effects. Multiple covariance structures were tested and the model fitting statistics were compared to determine the best fitting model. Mean separation was performed using the LSMEAN statement and comparisons between treatments were performed with the Tukey-Kramer test. Data are shown as least-squares mean [+ or -] SEM. Other data were analyzed as a completely randomized design. Mean comparison was performed by Duncan's multiple range test and a p value less than 0.05 was considered statistically significant.

[FIGURE 1 OMITTED]

RESULTS

In the testing of the main effects of some variables such as FI, WI and weight gain, the effects of week and interaction were significant; that was expected and is due to the nature of these variables and to the environmental effects. Thus, comparison between treatments in each week was considered as an appropriate contrast.

[FIGURE 2 OMITTED]

Data analyses showed that hypoinsulinemia caused a dose-dependent increase in FI where it was greater by 242, 388.8 and 290 g in group M vs the control group in weeks 5 to 7, respectively (Figure 1A). However, group L showed an incremental effect but this was not significant (p>0.05). WI in groups M and L was greater than in the control group in weeks 5 and 6 (Figure 1B). In addition, total WI (as the sum of WI and 10% of FI) in group M was also greater than in the control group in week 5 (Figure 1C). FI/BW ratio in group M significantly increased in weeks 6 and 7 compared to the control group (Figure 1D). STZ-groups gained less weight than the control group (p<0.05), especially in group L, where it was 2.06, 1.67 and 2.36 kg in week 5 and 2.24, 1.67 and 2.36 kg in week 6 for groups M, L and the control, respectively (Figure 1E). Weight gain /body weight ratio in group M was lower than in the control group at nonsignificant levels in weeks 5 to 7 (Figure 1F), while it was significantly lower for group L in weeks 5 to 8. FCR in group M was greater than in the control group in weeks 5 and 7. Interestingly, FCR in group L was markedly greater than in groups M and C in weeks 5 and 6 (Figure 1G).

As expected, blood glucose concentrations were increased by STZ injection in a dose-dependent manner (p<0.05), especially in weeks 4, 6 and 7 (Figure 2A). Glucose concentration reached 116.6 mg/dl in group M vs. 81.2 mg/dl in the control group in week 4. Hypertriglyceridemia was observed in groups L and M when compared with the control group in weeks 7 and 8 (Figure 2B). Blood cholesterol levels in group M were significantly greater than in the control group during weeks 5 to 8 (Figure 2C); significantly increased cholesterol level was also observed for group L in weeks 5 and 8. Blood TP levels in group M showed significant increase as against the control group in weeks 4 to 8 (Figure 2D) and also vs. group L in weeks 4, 6 and 8 (p<0.05). Albumin concentrations in groups M and L, however, were increased after injection of STZ, but these were not significant except in week 8 (Figure 2E). BUN concentrations (Figure 2F) in group M were elevated significantly compared to the control group in the two final weeks (9.78 vs. 2 and 17.92 vs. 14.89 in weeks 7 and 8, respectively). KB concentrations in group M were greater than in the control group in weeks 4 and 7 (Figure 2G).

[FIGURE 3 OMITTED]

Fasted insulin levels in group M showed a dosedependent decrease (p<0.05), especially in weeks 4, 6 and 8 (Figure 3A). In diabetic animals of group M, insulin level declined up to 52, 65 and 20 percent of that in control animals in weeks 4, 6 and 8, respectively. Post-prandial insulin levels in groups M and L declined significantly compared with the control group in week 4, but in the two final weeks the control group showed lower insulin levels than other groups (Figure 3B). Leptin concentrations in groups M and L markedly declined compared to the control group in the post-injection interval except in week 5 (Figure 3C). However, this decline was not observed for postprandial leptin concentrations (Figure 3D).

Heart rate, rectal temperature and EBW showed no significant differences between treatment groups. Urinary glucose showed a dose-dependent increase between groups, however, decline was not significant (p = 0.351). Interestingly, DM of liver in group M was significantly lower than other groups but for meat, it was significantly greater. There were no significant differences between CP and crude fat contents of all groups for both liver and meat (Table 1).

It must be noted that during the final week of the experiment (week 8), a heavy snowfall occurred that led to cessation of the experiment and results for this week do not have congruity with those of previous weeks. This is completely revealed in all three figures.

DISCUSSION

The brain monitors energy states by receiving continuous information from the periphery or other regions of the brain. With regard to appetite, there are at least two major categories including orexigenic signals such as NPY, AgRP, orexin and opioid peptides that stimulate appetite while anorexigenic signals such as insulin, leptin and [alpha]-MSH exert inhibitory effects on appetite and suppress it. The regulation of appetite is derived through these opposing signals and the resultant interaction consequently determines appetite (Schwartz et al., 2000; Gerozissis, 2004; Niswender et al., 2004; Broberger, 2005; Woods, 2005).

Insulin is an important and potent anorexigenic signal in energy homeostasis. It is mainly known for its peripheral effects on the metabolism of glucose, fat and protein where it facilitates the storage of energy sources mainly in the form of fat and/or glycogen (Carlon and Campbell, 1993; Niswender et al., 2004). In the brain, insulin exerts a catabolic action by suppressing appetite. Secretion and release of two potent orexigenic peptides, NPY and AgRP, are inhibited by insulin (Sipols et al., 1995; Saho et al., 1997; Henry et al., 1999; Sorensen et al., 2002; Breen et al., 2005), while [alpha]-MSH secretion is induced (Benoit et al., 2002; Sorensen et al., 2002; Breen et al., 2005). Furthermore, insulin is a potent secretagogue of leptin that has a close partnership with insulin in control of appetite (Barr et al., 1997; Saltiel and Kahn, 2001). The opposing effects of insulin in the periphery and in the brain are evident in diabetes. In this situation, lack of peripheral, anabolic action of insulin is accompanied by the lack of its central, catabolic action that results in hyperglycemia and polyuria along with excess demand for feeding known as diabetic hyperphagia. STZ-induced diabetes in rodents caused hyperphagia, however, they could not gain weight normally because of inability to store blood metabolites in tissues (Hidaka et al., 2001; Morris and Pavia, 2004). Consequently, the metabolites are excreted via urine.

In the present study, diabetic animals--in particular group M, showed diabetic hyperphagia in weeks 5 to 7 that was consistent with results obtained in rodents (Roland and Caputo, 1985; Smith and Gannon, 1991; Hidaka et al., 2001; Barber et al., 2003; Akirav et al., 2004; Morris and Pavia, 2004). Diabetic lambs showed hyperphagia with lower severity than observed in diabetic rodents. Physical satiety, however, may be a logical reason for this, because in terms of kind of feeds consumed by ruminants, they face gut fullness that prevents more feeding. As reported for rodents and humans (Barr et al., 1997; Boden et al., 1997), in the present study the regulatory role of insulin in leptin secretion was revealed where the hypoinsulinemia in the post-injection interval paralleled hypoleptinemia, however, it was seen for fasted animals. Nonetheless, declined insulin and leptin levels in group M can be considered as an important factor in hyperphagia. Previous study in sheep showed the anorexigenic effect of leptin on appetite (Henry et al., 1999).

In spite of increased FI, diabetic animals were unable to gain weight even at the level of intact animals. Indeed, diabetic animals lost weight when compared with the control group. Similar results were observed in rodents (Hidaka et al., 2001; Morris and Pavia, 2004) and cattle (Higdon et al., 2001). It is obviously due to the inability of peripheral tissues to uptake metabolites from the bloodstream.

One week after induction of diabetes, WI and TWI increased, especially in group M. This was in agreement with increased WI observed in rats that was reported to be mainly because of elevated urine volume and, in part, of enhanced noradrenalin levels in the hypothalamus (Smith and Gannon, 1991; Barber et al., 2003; Morris and Pavia, 2004).

As observed in rodents and humans, diabetic animals in group M showed hyperglycemia, hypertriglyceridemia and (to a lower extent) hyperproteinemia that can be considered as results of hyperphagia and also the lack of blood metabolites entering into the tissues. In fact, it revealed the lack of a peripheral, anabolic role of insulin. It was confirmed by the glycosuria and proteinuria (data not shown) observed in these animals. Similarly, induction of diabetes was accompanied by hypertriglyceridemia in rodents (Junod et al., 1969; Sambandam et al., 2000; Morris and Pavia, 2004) and sheep (Mamo et al., 1983). Proteinuria was observed in STZ-diabetic sheep reflecting increased blood TP concentrations (Ramanathan et al., 2004).

In the present study, FCR in diabetic animals was greater than in the control group, meaning that diabetic animals are less efficient in converting consumed feed into weight gain. It was not unexpected because diabetic animals were polyuric (visually but not measured quantitatively) with obvious glycosuria and proteinuria. As a result, retained-energy value (kcal of FI minus kcal of urinary glucose loss) in these animals decreased as observed in rodents (Willing et al., 1990).

Higher blood KB concentrations observed in diabetic animals (particularly group M) were not necessarily similar to those observed in diabetic rodents or humans as ketoacidosis, because diabetic animals consumed more feed producing more VFAs which a moiety of them is absorbed in the form of ketone bodies, in particular betahydroxybutyrate (Bergman, 1990; Gabel and Sehested, 1997). Nonetheless, it is difficult to distinguish these conflicting events from each others. The previous study in rodents showed occurrence of ketoacidosis using high doses of STZ (>100 mg/kg BW). Similar results were observed in diabetic sheep (Ramanathan et al., 2004) and cattle (Prior and Smith, 1983).

BUN concentrations in group M were greater than in the control group in the final two weeks. Prior and smith (1983) showed that diabetic cattle have higher BUN and creatinine levels. In the present study, elevated blood TP and BUN concentrations strongly imply that nitrogen metabolism was impaired with diabetes. This is mainly due to the lack of uptake of proteins by peripheral tissues and their denaturation.

Carcass and liver compositions did not differ among groups while feed intake and also insulin and leptin levels showed marked differences among them. In farm animals, fat and protein contents and their partitioning in body are influenced by nutritional states and hormonal profiles including insulin, leptin and growth hormone (Torbay et al., 1985; Olivares and Hallford, 1990; Roberts et al., 1994; Chung et al., 2008). Likely, enhanced feed intake counteracted wih lowered insulin and leptin levels in fat deposition. Lack of peripheral anabolic effect of insulin in diabetic animals of present study has no significant effect on EBW after dressing. It seems that attenuated anabolic effect of insulin in these animals was conpensated by hypherphagia.

Ruminants are less sensitive to insulin than monogastric animals (Sasaki and Takahashi, 1983; Sano and Terashima, 1991). On the other hand, secretion of insulin in ruminants is stimulated by VFAs, especially n-butyrate and propionate, and IV injection of these VFA acts as a strong stimulus of insulin secretion in sheep, goats and cattle (Matsunaga et al., 1999). In ruminants, a large proportion of energy requirements are supplied as VFAs, which are produced by the fermentation of dietary carbohydrates (Gabel and Sehested, 1997). Therefore, small quantities of glucose are absorbed from the small intestine and, as a consequence, glucose utilization in the whole-body is relatively dependant upon glucose production via gluconeogenesis in liver and other tissues (Sano et al., 1985).

Regardless of these profound differences between energy metabolism in ruminants and non-ruminants, in feeding patterns (e.g. time spent to eat and the numbers of meals), and also the diet composition (mainly due to energy density and fiber content of feed), it seems that there is close similarity in energy homeostasis in diabetic conditions of both species.

In the present study, injection of STZ caused hypoinsulinemia with a wide extent of abnormalities; in group H, the severity of diabetes was so intense that they were challenged for survival, in a manner that has been previously observed for cattle (Higdon et al., 2001), confirming the crucial role of insulin in energy balance and metabolism in ruminants. Diabetic hyperphagia and the inability for weight gain were observed in sheep, establishing the opposing anabolic and catabolic actions of insulin in these animals and suggesting that diabetic sheep are a useful animal model for investigating roles of insulin in energy homeostasis.

IMPLICATIONS

Before this study, there existed no work in which diabetes was induced with varying severity and a wide range of STZ doses. More studies are needed to determine the role of insulin in energy homeostasis and growth parameters of ruminants. It seems that the role of insulin in energy homeostasis of ruminants is more prominent than presumed for these animals and their lower blood glucose levels cannot attenuate its crucial roles.

Received October 21, 2008; Accepted February 23, 2009

REFERENCES

Air, E. L., S. C. Benoit, K. A. Blake Smith, D. J. Clegg and S. C. Woods. 2002. Acute third ventricular administration of insulin decreases food intake in two paradigms. Pharmacol. Biochem. Behav. 72:423-429.

Akirav, E. M., O. Chan, K. Inouye, M. C. Riddell, S. G. Matthews and M. Vranic. 2004. Partial leptin restoration increases hypothalamic-pituitary-adrenal activity while diminishing weight loss and hyperphagia in streptozotocin diabetic rats. Metabolism 53:1558-1564.

Barber, M., B. S. Kasturi, M. E. Austin, K. P. Patel, S. M. J. MohanKumar and P. S. MohanKumar. 2003. Diabetes-induced neuroendocrine changes in rats: Role of brain monoamines, insulin and leptin. Brain Res. 964:128-135.

Barr, V. A., D. Malide, M. J. Zarnowski, S. I. Taylor and S. W. Cushman. 1997. Insulin stimulates both leptin secretion and production by rat white adipose tissue. Endocrinol. 138:4463-4472.

Benoit, S. C., E. L. Air, L. M. Coolen, R. Strauss, A. Jackman, D. G. Clegg, R. J. Seeley and S. C. Woods. 2002. The catabolic action of insulin in the brain is mediated by melanocortins. J. Neurosci. 22:9048-9052.

Bergman, E. N. 1990. Energy contributions of volatile fatty acids from the gastrointestinal tract in various species. Physiol. Rev. 70:567-575.

Boden, G., X. Chen, J. W. Kplaczynski and M. Polansky. 1997. Effects of prolonged hyperinsulinemia on serum leptin in normal human subjects. J. Clin. Invest. 100:1107-1113.

Breen, L. T., I. M. Conwell and S. L. Wardlaw. 2005. Effects of fasting, leptin and insulin on AGRP and POMC peptide release in the hypothalamus. Brain Res. 1032:1414-1418.

Broberger, C. 2005. Brain regulation of food intake and appetite: molecules and networks. J. Intern. Med. 258:301-307.

Carlon, M. G. and P. J. Campbell. 1993. Intensive insulinterapy and weight gain in IDDM. Diabetes 42:1700-1707.

Chung, E. R., S. C. Shin and K. Y. Chung. 2008. SNP discovery in the leptin promoter gene and association with meat quality and carcass traits in korean cattle. Asian-Aust. J. Anim. Sci. 21:1689-1695.

Foster, L. A., N. K. Ames and R. S. Emery. 1991. Food intake and serum insulin responses to intraventricular infusions of insulin and IGF-I. Physiol. Behav. 50:745-749.

Gabel, G. and J. Sehested. 1997. SCFA transport in the forestomach of ruminants. Comp. Biochem. Physiol. 118:367-374.

Gerozissis, K. 2004. Brain insulin and feeding: a bi-directional communication. Eur. J. Pharmacol. 490:59-70.

Henry, B. A., J. W. Goding, W. S. Alexander, A. J. Tilbrook, B. J. Canny, F. Dunshea, A. Rao, A. Mansell and I. J. Clarke. 1999.

Central administration of leptin to ovariectomized ewes inhibits food intake without affecting the secretion of hormones from pituitary gland: evidence for a dissociation of effects on appetite and neuroendocrine function. Endocrinol. 140:1175-1182.

Hidaka, S., H. Yoshimatsu, S. Kondou, K. Oka, Y. Tsuruta, H. Sakino, E. Itateyama, H. Noguchi, K. Himeno, K. Okamoto, Y. Teshima, T. Okeda and T. Sakata. 2001. Hypoleptinemia, but not hypoinsulinemia, induced hyperphagia in streptozotocin-induced diabetic rat. J. Neurochem. 77:993-1000.

Higdon III, H. L., P. G. Parnel and J. C. Spitzer. 2001. Streptozotocin-induced pancreatic islet destruction in beef cows. Vet. Pathol. 38:715-720.

Junod, A., A. E. Lambert, W. Stauffacher and A. E. Renold. 1969. Diabetogenic action of streptozotocin: Relationship of dose to metabolic response. J. Clin. Invest. 48:2129-2139.

Mamo, J. C., A. M. Snowell and D. L. Topping. 1983. Plasma triacylglycerol secretion in sheep. Paradoxical effects of fasting and alloxan diabetes. Biochem. Biophys. Acta. 753:272-275.

Matsunaga, N., N. T. Arakawa, T. Goda, K. T. Nam, A. Ohneda, Y. Sasaki and K. Katoh. 1999. Effects of ruminal infusion of volatile fatty acids on plasma concentration of growth hormone and insulin in sheep. Domest. Anim. Endocrinol. 17:17-27.

Morris, M. J. and J. M. Pavia. 2004. Increased endogenous noradrenaline and neuropeptide Y release from the hypothalamus of streptozotocin diabetic rats. Brain Res. 1006:100-106.

Niswender, K. D., D. G. Baskin and M. W. Schwartz. 2004. Insulin and its evolving partnership with leptin in the hypothalamic control of energy homeostasis. Trend in Endocrinol. Metab. 15:362-369.

NRC. 1985. Nutrient requirement of sheep. 6th Rev. Ed. National Academy of Science, Washington, DC.

Olivares, V. H. and D. M. Hallford. 1990. Growth and carcass characteristics and serum growth hormone, prolactin and insulin profiles in Debouillet lambs treated with ovine growth hormone and (or) zeranol. J. Anim. Sci. 68:1971-1979.

Patel, B. K., J. I. Koenig, L. M. Kaplan and S. C. Hooi. 1998. Increase in plasma leptin and Lep mRNA concentrations by food intake is dependent on insulin. Metabolism 47:603-607.

Prior, R. L. and S. T. Smith. 1983. Role of insulin in regulating amino acid metabolism in normal and alloxan-diabetic cattle. J. Nutr. 113:1016-1031.

Ramanathan, T., S. Morita, Y. Huang, K. Shirota, T. Nishimura, X. Zheng and S. N. Hunyor. 2004. Glucose-insulin-potassium solution improves left ventricular energetics in chronic ovine diabetes. Ann. Thorac. Surg. 77:1408-1414.

Roberts, T. J., M. J. Azain, G. J. Hausman and R. J. Martin. 1994. Interaction of insulin and somatotropin on body weight gain, feed intake, and body composition in rats. Am. J. Physiol. Endocrinol. Metab. 267:E293-E299.

Roland, N. and F. A. Caputo. 1985. Voluntary exercise, food intake, and plasma metabolites in streptozotocin-diabetic Syrian hamsters. Physiol. Behav. 34:635-640.

Sahu, A., C. A. Sninsky and S. P. Kalra. 1997. Evidence that hypothalamic neuropeptide Y gene expression and NPY levels in the paraventricular nucleus increase before the onset of hyperphagia in experimental diabetes. Brain Res. 755:339-342.

Saltiel, A. R. and C. R. Kahn. 2001. Insulin signaling and the regulation of glucose and lipid metabolism. Nature 414:799-806.

Sambandam, N., M. A. Abrahani, S. Craig, O. Al-Atar, E. Jeon and B. Rodrigues. 2000. Metabolism of VLDL is increased in streptozotocin-induced diabetic rat hearts. Am. J. Physiol. Heart 278:1874-1882.

Sano, H. and Y. Terashima. 1991. Insulin responsiveness to glucose and tissue responsiveness to insulin in cows, sheep and pigs. Asian-Aust. J. Anim. Sci. 4:41-45.

Sano, H., K. Takahashi, K. Ambo and T. Tsuda. 1985. Rates of blood glucose appearance and disappearance during hyperglycemia induced by alloxan in sheep. Tohoko J. Agri. Res. 36:9-15.

SAS. 1996. SAS/STAT[R] software; Changes and Enhancements through Release 6.11. SAS Inst. Inc., Cary, NC.

Sasaki, Y. and H. Takahashi. 1983. Insulin response to secretagogues in sheep exposed to cold. J. Physiol. (London) 334:155-167.

Schwartz, M. W., A. J. Sipols, J. L. Marks, G. Sanacora, J. D. White, A. Schurink, S. E. Kahn, D. G. Baskin, S. C. Woods, D. Figlewicz and Jr. Porte. 1992. Inhibition of hypothalamic NPY gene expression by insulin. Endocrinol. 130:3608-3616.

Schwartz, M. W., S. C. Woods, D. J. Porte, R. J. Seeley and D. G. Baskin. 2000. Central nervous system control of food intake. Nature 404:661-671.

Shan, T., Y. Wang, J. Gua, X. Chu, J. Liu and Z. Xu. 2008. The body weight-related differences of leptin and neuropeptide Y (NPY) gene expression in pigs. Asian-Aust. J. Anim. Sci. 21:161-166.

Sipols, A. J., D. G. Baskin and M. W. Schwartz. 1995. Effect of intracerebroventricular insulin infusion on diabetic hyperphagia and hypothalamic neuropeptide gene expression. Diabetes 44:147-151.

Smith, J. C. and K. S. Gannon. 1991. Ingestion patterns of food, water, saccharin and sucrose in streptozotocin-induced diabetic rats. Physiol. Behav. 49:189-199.

Sorensen, A., A. L. Adam, P. A. Findlay, M. Marie, L. Thomas, M. T. Travers and R. G. Vernon. 2002. Leptin secretion and hypothalamic neuropeptide and receptor gene expression in sheep. Am. J. Physiol. Reg. Integ. Comp. Physiol. 282:R1227-R1235.

Thomas, L. 1998. Clinical laboratory diagnostics. 1st Ed. Frankfurt: TH-Books Verlagsgesellschaft.

Torbay, N., E. F. Bracco, A. Geliebter, I. M. Stewart and S. A Hashim. 1985. Insulin increases body fat despite control of food intake and physical activity. Am. J. Physiol. Regul. Integr. Comp. Physiol. 248:R120-R124.

Willing, A. E., E. K. Walls and H. S. Koopman. 1990. Insulin infusion stimulates daily food intake and body weight gain in diabetic rats. Physiol. Behav. 48:893-898.

Woods, S. C., E. C. Lotter, L. D. McKay, D. Jr. Porte. 1979. Chronic intracerebroventricular infusion of insulin reduces food intake and body weight of baboons. Nature 282:503-505.

Woods, S. C. and D. J. Porte. 1977. Relationship between plasma and cerebrospinal fluid levels of dogs. Am. J. Physiol. 233:331-334.

Woods, S. C. 2005. Signals that influence food intake and body weight. Physiol. Behav. 86:709-716.

Moslemipur F. *, Torbatinejad N. M., Khazali H. (1), Hassani S. and Ghoorchi T.

Department of Animal Science, Gorgan University of Agricultural Sciences and Natural Resources, Gorgan, Iran

* Corresponding Author: Moslemipur F. Tel: +98-171-2220320, Fax: +98-171-4420981, E-mail: moslemipurf@gau.ac.ir

(1) Division of Physiology, Department of Biology, Shahid Beheshti University, Tehran, Iran.
Table 1. Composition of liver (cranial lobe) and meat (fillet of
vertebra 12) of experimental lambs in terms of DM, and CP and fat
contents as a percent of DM (1)

Variable p value Means (2)

 C L M

Liver DM (%) 0.0061 36.23 (a) 29.68 (a) 19.20 (b)
 CP (% DM) 0.3464 58.72 (a) 60.44 (a) 60.36 (a)
 Fat (%DM) 0.3964 10.83 (a) 12.14 (a) 10.42 (a)
Meat DM (%) 0.1346 42.90 (b) 41.64 (b) 44.61 (a)
 CP (% DM) 0.4643 55.22 (a) 50.83 (a) 54.66 (a)
 Fat (% DM) 0.9232 35.15 (a) 36.22 (a) 35.96 (a)

(1) Group H could not continue the experiment.

(2) Comparison was performed by Duncan's multiple range test after
ANOVA. Means within rows with no common superscript letters are
significantly different.
COPYRIGHT 2009 Asian - Australasian Association of Animal Production Societies
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2009 Gale, Cengage Learning. All rights reserved.

Article Details
Printer friendly Cite/link Email Feedback
Author:Moslemipur, F.; Torbatinejad, N.M.; Khazali, H.; Hassani, S.; Ghoorchi, T.
Publication:Asian - Australasian Journal of Animal Sciences
Article Type:Report
Geographic Code:7IRAN
Date:Jun 1, 2009
Words:5087
Previous Article:Linolenic acid in association with malate or fumarate increased CLA production and reduced methane generation by rumen microbes.
Next Article:Potential benefits of intercropping corn with runner bean for small-sized farming system.
Topics:


Related Articles
The hunger hormone? An appetite stimulant produced by the stomach may lead to treatments for obesity and wasting syndromes.
The body weight-related differences of leptin and neuropeptide Y (NPY) gene expression in pigs *.
Effect of monensin and live yeast supplementation on growth performance, nutrient digestibility, carcass characteristics and ruminal fermentation...
Effects of dietary copper source and level on performance, carcass characteristics and lipid metabolism in lambs *.
Effects of chromium yeast on performance, insulin activity, and lipid metabolism in lambs fed different dietary protein levels *.
Development of bovine specific leptin radioimmunoassay and relationship of plasma leptin with vitamin A and age of Wagyu.
SNP discovery in the leptin promoter gene and association with meat quality and carcass traits in Korean cattle.
The effects of docking on growth traits, carcass characteristics and blood biochemical parameters of Sanjabi fat-tailed lambs.
Endocrine regulation of energy metabolism: review of pathobiochemical and clinical chemical aspects of leptin, ghrelin, adiponectin, and resistin.
Adiponectin and leptin in maternal serum, cord blood, and breast milk.

Terms of use | Privacy policy | Copyright © 2019 Farlex, Inc. | Feedback | For webmasters