Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “LACTATION”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 379 records · Page 21Linked to original sources

Induction of lactation: lactational, physiological, and hormonal responses in the bovine.

Milk yields, physiological responses, and concentrations of plasma hormones were evaluated in 24 attempts to induce lactation in nonlactating dairy cows. Subcutaneous injections of estradiol-17beta and progesterone (.10 and .25 mg/kg body weight per day) for 7 consecutive days were used. Dexamethasone injections (.028 mg/kg body weight per day) on days 18 to 20 were given during 12 attempts at induction. Milking was initiated on day 21. All cows showed proestrus activity within 2 days after the first steroid injection; this subsided, then reappeared in many animals between days 16 to 20. In 14 of 24 attempts mean daily milk production was greater than 5 kg. Actual or projected 305-day lactation milk yields were between 1859 and 5354 kg. However, milk yields of seven induced cows averaged only 73% (32% to 136% range) of their previous natural lactations. Dexamethasone injections increased the number of cows that produced more than 5 kg/day; however, milk yields were not improved. Concentrations of estradiol, estrone, and progesterone in plasma were unaffected by dexamethasone, but concentrations of glucocorticoids in plasma were depressed on days 19 to 22. Concentrations of prolactin (peak and mean) in plasma for six cows each that produced greater or less than 5 kg/day did not differ. However, concentrations of prolactin increased in the week following steroid injections (days 8 to 15) only in those cows that produced greater than 5 kg/day but were elevated in all cows during the 3rd wk.

Animals↗

Artificial induction of lactation in cattle: initiation of lactation and estrogen and progesterone concentrations in milk.

Thirty heifers were given 11 subcutaneous injections of 5 mg estradiol benzoate and 200 mg progesterone every 3 d to develop their mammary glands. Three days later groups of animals were treated with 1) 20 mg dexamethasone twice, 2) 500 micrograms cloprostenol thrice, 3) dexamethasone and cloprostenol, 4) oxytocin 4 IU six times, or 5) no further injections. Two further groups of six heifers each (6 and 7) were treated in a manner similar to groups 1 and 3 except the dose of estrogen to develop their mammary glands was doubled to 10 mg/3 d. Six lactating first calf heifers were controls (8). The proportion of animals lactating, combined milk yield for each group (kg), and mean days lactated were 1) 5/6, 3831, 142; 2) 1/6, 912, 195; 3) 6/6, 4898, 194; 4) 3/6, 1066, 128; 5) 1/6, 293, 154; 6) 6/6, 6109, 130; 7) 6/6, 6265, 130; and 8) 6/6, 19, 190, 251. The lactogenic response to dexamethasone and oxytocin is similar to that in sheep, but the response to cloprostenol indicates a species difference. Intensive blood sampling before and after injection of hormones, intended to trigger lactogenesis, showed that plasma prolactin rose to peaks above 210 ng/ml in cows of groups 2, 3, and 4 and were unchanged from the base below 40 ng/ml in groups 1 and 5. Monitoring of steroids after induction treatment showed estradiol-17 beta ranged between 35 and 400 pg/ml and 20 to 80 pg/ml in mammary secretion and plasma and progesterone concentrations were less than at diestrus.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

Lactation curves for first lactation Egyptian buffalo.

First lactation records of 1538 buffalo maintained at the Animal Production Research Institute farms in 1967 to 1990 were used to determine lactation curves for three lactation lengths: > 28 and < 150 d, > 149 d, and > or = 308 d, as well as all records. Daily milk yields were summed by 14-d intervals for analyses. Yields peaked at the first, fifth, sixth, and seventh periods for > 28 and < 150 d, > 149 d, > or = 308 d, and all records. Herd-year-season significantly affected milk yield in all periods. Persistency for all records and three groupings (> 28 d, > 149 d, and > or = 308 d in milk) was highest for the > or = 308-d group (1.02 vs. .85 for > 149 d, .57 for > 28 d, and .47 for all records). Herd-year-season of calving significantly affected persistency in all records and the three subset groupings. Persistency was higher for buffalo calving in spring and summer for all records, records > 28 d, and records > 149 d but in summer and autumn for the > or = 308 d, the correlation coefficient between persistency and milk yield (r = .06) was not significant but was negative with season of calving (r =-.11).

Aging↗

Effectiveness of acidic calcium sulfate with propionic and lactic acid and lactates as postprocessing dipping solutions to control Listeria monocytogenes on frankfurters with or without potassium lactate and stored vacuum packaged at 4.5 degrees C.

The safety of ready-to-eat meat products such as frankfurters can be enhanced by treating with approved antimicrobial substances to control the growth of Listeria monocytogenes. We evaluated the effectiveness of acidic calcium sulfate with propionic and lactic acid, potassium lactate, or lactic acid postprocessing dipping solutions to control L. monocytogenes inoculated (ca. 10(8) CFU/ml) onto the surface of frankfurters with or without potassium lactate and stored in vacuum packages at 4.5 degrees C for up to 12 weeks. Two frankfurter formulations were manufactured without (control) or with potassium lactate (KL, 3.3% of a 60% [wt/wt] commercially available syrup). After cooking, chilling, and peeling, each batch was divided into inoculated (four strains of L. monocytogenes mixture) and noninoculated groups. Each group was treated with four different dips: (i) control (saline solution), (ii) acidic calcium sulfate with propionic and lactic acid (ACS, 1:2 water), (iii) KL, or (iv) lactic acid (LA, 3.4% of a 88% [wt/wt] commercially available syrup) for 30 s. Noninoculated frankfurters were periodically analyzed for pH, water activity, residual nitrite, and aerobic plate counts (APCs), and L. monocytogenes counts (modified Oxford medium) were determined on inoculated samples. Surface APC counts remained at or near the lower limit of detection (<2 log CFU per frank) on franks with or without KL and treated with ACS or LA throughout 12 weeks at 4.5 degrees C. L. monoctogenes counts remained at the minimum level of detection on all franks treated with the ACS dip, which indicated a residual bactericidal effect when L. monocytogenes populations were monitored over 12 weeks. L. monocytogenes numbers were also reduced, but not to the same degree in franks made without or with KL and treated with LA. These results revealed the effectiveness of ACS (bactericidal effect) or LA (bacteriostatic effect) as postprocessing dipping solutions to inhibit or control the growth of L. monocytogenes on vacuum-packaged frankfurters stored at 4.5 degrees C for up to 12 weeks.

Animals↗

[First evaluation of plasma L-lactate measurements by means of the "lactate analyzer 5400"].

The instrument used can measure lactate instantaneously by a semi-automatic method using an electrochemical-enzymatic sensor. In order to test the instrument, 3 series of measurements were carried out simultaneously by the Analyzer and by the conventional enzymatic method (Boehringer, Mannheim): "normal" plasma and "normal" blood was obtained from venous blood of healthy adults; pathological plasma, obtained by addition of a known concentration of lactate to normal plasma, was also tested. The correlation curves for these three series are reported. The coefficient r is between 0.95 and 0.98, which bears out the reliability of the measurements. Since a short period, this lactate analyzer is used in our research laboratory in obstetrics.

Autoanalysis↗

Role of compensatory growth in lactation: a stair-step nutrient regimen modulates differentiation and lactation of bovine mammary gland.

Twenty Holstein heifers were assigned to either a control or test (stair-step compensatory; food restriction, followed by refeeding) growth group. The stair-step growth model was designed to induce distinctive compensatory allometric mammary development during three different hormonal states, coinciding with prepubertal, pubertal, and late gestational stages. Mammary tissues obtained by biopsy from pregnant and lactating cows were used for acini culture and chemical composition analysis. Test mammary tissues from late gestation heifers contained less (P = .067) fat than control counterparts (731 vs. 628 mg/g). DNA, RNA, and protein contents in test mammary tissue from late gestation cows were higher (P = .001 to .088) compared to control tissue. Milk protein secretion of test acini in culture was increased more than 20% over that of the control acini. Lactating mammary acinar cells in culture from test cows exhibited a 14% increase in amino acid uptake over that of the control. RNA dot-blot hybridization analysis revealed that alpha s1- and beta-casein mRNA accumulation in acini from test tissue was increased (P = .027 to .042) as much as 40-50%. During both food restriction and refeeding, concentrations of plasma growth hormone were elevated. Food restriction decreased levels of plasma insulin, whereas levels of insulin were elevated during refeeding. The long-term influence of compensatory growth upon subsequent lactation performance was also evaluated. Milk production data derived from previous two sequential growth trials showed that cows from test groups produced approximately 10% more (P = .001) milk compared to control counterparts. Results reinforce our postulation that compensatory growth induced by nutritional modulation regulates the differentiation and functional activity of the mammary gland.

Animal Nutritional Physiological Phenomena↗

Lactate kinetics estimated by single injection and continuous infusion of [14C-(U)]-lactate in rats.

1 Identical values of the rate of lactate turnover determined with [14C-(U)]-lactate were found with single injection or continuous infusion techniques in anaesthetized and mechanically ventilated rats. 2 The mean transit time and total minimal body mass of lactate determined graphically (Katz et al., 1974 a, b) were higher with single injection than with continuous infusion of the tracer.

Animals↗

Thin-layer agarose electrophoresis of lactate dehydrogenase isoenzymes in serum: a note on the method of reporting and on the lactate dehydrogenase isoenzyme-1/isoenzyme-2 ratio in acute myocardial infarction.

We assessed the clinical efficacy of a thin-layer agarose electrophoresis assay for lactate dehydrogenase isoenzyme estimation in the diagnosis of acute myocardial infarction. From a population of 228 patients admitted to the Coronary Care Unit with suspected acute myocardial infarction, all 101 positive cases (confirmed by clinical presentation and electrocardiographic changes) were correctly identified with lactate dehydrogenase isoenzyme-1 percentage of total activity above the reference range and with a lactate dehydrogenase isoenzyme-1/isoenzyme-2 ratio of 0.76 or above. This ratio was between 0.45 and 0.74 for 250 healthy subjects. No falsely negative, but 12 falsely positive results were obtained from this Coronary Care Unit population, to give a sensitivity of 100% and a specificity of 90.5% for the ratio test.

Clinical Enzyme Tests↗

Prefeeding plasma acetoacetate and glucose in healthy, lactating heifers. Variations related to milk yield, metabolic balances and stage of lactation.

When measured before morning feeding plasma acetoacetate (ACAC) increased and glucose (GL) decreased significantly with increasing milk yield (fat corrected, FCM) within 2 groups of half-sister related heifers which did not suffer from clinical ketosis. The groups received respectively A: 7 kg and B: 4 kg/d of concentrates in addition to grass silage ad libitum (each group 88 animals). Correlation coefficients of the same magnitude between the 3 variables mentioned were obtained in the 1st and 3rd month of lactation in spite of a narrowing of the ACAC range from 0.024-0.66 to 0.019-0.16 mmol/l. Reproducibility of differences between animals in milk yield and in the plasma components was evidenced by significant correlations between measurements in the 1st and 3rd month. The B-animals produced 2.4 kg/d less FCM than the better fed A group (A, 1st month of lactation 19.8 +/- 3.1 kg/d) while the mean values for ACAC and GL remained practically unaffected by the difference in feeding. B cows gave consistently 5-6% lower GL means (p < 0.01) than A animals with identical yields. Animals which showed marked ACAC increment during the first 5-6 weeks of lactation produced 3-4 kg more FCM/d than equally fed animals with constantly low ACAC levels. The estimated energy deficit of this ketonaemic, high-producing category corresponded to the production of 4.5-6 kg FCM/d from body reserves. Low ACAC values (< 0.05 mmol/l) were reproduced with a standard deviation of +/- 4% with the automated nitroprusside method described.

Acetoacetates↗

Vascular architecture of the lactating and non-lactating teat of the bitch: a scanning electron- and light microscope study.

Tissues from fourteen mammary glands of eight bitches were prepared for scanning electron microscopy of vascular corrosion casts and for histology to study the vasculature of the lactating and non-lactating teats. The densely-meshed mammary dermal capillary network formed ridges and troughs. The teat ducts were vascularized by a relatively densely-meshed capillary network which drained into veins longitudinally oriented to the ducts. Between eight and fifteen teat duct openings were seen on the tip of the teat, that were sometimes divided by a septum. The inner vascularization of the teat showed that the main papillary arteries divided into undulating secondary papillary arteries which presented numerous semi-constrictions and loops. Their structure may help during erection of the teat. Arteriovenous anastomoses found at different points may participate in blood flow maintenance during suckling, heat regulation and teat erection. Veins freely anastomosed and ran longitudinally to the axis of the teat. They exhibited numerous bicuspid valves. In non-lactating teats, vessels showed the same main architecture and characteristics mentioned above, although these were considerably less marked. The structure of the vascular elements in the teat of the bitch could favor blood flow during suckling and suggest that vessels adapt to the physiological situation.

Animals↗

Human testis-specific lactate dehydrogenase-C promoter drives overexpression of mouse lactate dehydrogenase-1 cDNA in testes of transgenic mice.

The three isozymes of lactate dehydrogenase, each encoded by a separate gene, are developmentally regulated and differentially expressed in tissue-specific patterns. The lactate dehydrogenase-C (LDHC, mouse Ldh3) gene is temporally expressed exclusively in the germ line during spermatogenesis, whereas lactate dehydrogenase-A (LDHA, mouse Ldh1) and B (LDHB, mouse Ldh2) genes are active in somatic tissues. To determine, therefore, whether overexpression of Ldh1 would perturb spermatogenesis, we constructed a transgene in which a sequence from the promoter region of human LDHC was coupled with mouse Ldh1 cDNA. Among nine (three males, six females) founder lines that were identified as being transgenic for the construct, one male transmitted the gene through its germ line. Homo- and heterotetramers containing the LDH-A subunit were detected in homogenates of testes from transgenic animals. We conclude that the human LDHC promoter contains the necessary regulatory sequence(s) for specific expression of mouse Ldh1 as a transgene during spermatogenesis. The fertility of the founder animal was not impaired.

Animals↗

Improved Cytoplasmic pH Regulation, Increased Lactate Efflux, and Reduced Cytoplasmic Lactate Levels Are Biochemical Traits Expressed in Root Tips of Whole Maize Seedlings Acclimated to a Low-Oxygen Environment.

We tested the hypothesis (J.-H. Xia and P.H. Saglio [1992] Plant Physiol 100: 40-46) that the enhanced ability of maize (Zea mays) root tips to survive anoxia, elicited by a 4-h exposure to 3% O2 ("acclimation"), is due to less cytoplasmic acidosis early in anoxia. Cytoplasmic pH and fermentation reactions were monitored in excised and intact (attached) maize root tips by simultaneous in vivo 13C- and 31P-NMR spectroscopy. We demonstrate that both excised and intact acclimated root tips have significantly higher cytoplasmic pH values under anoxia. This reduction in cytoplasmic acidosis is greater in intact root tips. Remarkably, cytoplasmic pH does not change when root tips are transferred from 3% O2 to anoxia. The earlier observation of considerable lactate efflux and lowered intracellular lactate in excised, acclimated root tips (ibid.) was extended to intact seedlings. The predominant fermentation end product retained in the cells of acclimated root tips is alanine. We discuss the relationship between cytoplasmic pH and levels of intracellular lactate and alanine in sugar-replete roots, and the role of cytoplasmic pH in determining survival under anoxia.

Journal Article↗

Determination of lactate threshold by respiratory gas exchange measures and blood lactate levels during incremental load work.

OBJECTIVE: The purpose of this investigation was the determination of the lactate threshold (LT) by selected respiratory gas exchange measures and venous blood lactate levels during incremental load work on a mechanically braked cycle ergometer. DESIGN: Repeated measures design. SETTING: Human Performance Laboratory. PARTICIPANTS: Eight healthy trained soccer players (mean age 21.9 +/- 3.0 yr, mean VO2max = 59.2 +/- 3.6 ml.kg.min-1). OUTCOME MEASURE: Subjects conducted two incremental load work tests. Incremental load work was increased by 1 kilopond (kp) every third minute at 60 rpm until voluntary exhaustion. Blood samples from a forearm vein were collected during the second trial (T2) only and analyzed for lactic acid [LA-]. RESULTS: One-way analysis of variance (ANOVA) with repeated measures indicated no statistically significant difference between the two tests for maximal oxygen uptake (VO2max), maximal carbon dioxide production (VCO2max), maximal heart rate (HRmax), maximal pulmonary ventilation (VEBTPSmax) and lowest ventilatory equivalent of oxygen (VE/VO2), respectively; however, there was a significant difference among the oxygen uptake (VO2) values at the LT for the four determination methods. In our subjects, the measured (mean +/- SD) VE/VO2 in relation to VO2 for the first trial (T1) of 22.9 +/- 1.9 occurred at VO2 of 1.27 +/- 0.8 l.min-1. The lowest VE/VO2 and the onset of [LA-] accumulation calculated from individual exponential equations relating VE to VO2 yielded VO2 values of 1.77 +/- 0.18 and 1.74 +/- 0.25 l.min-1 for the T2. Utilizing natural log for lactate ln [LA-] to natural log for ln (VO2) equations, the LT for T2 occurred at VO2 of 1.30 +/- 0.70 l.min-1. CONCLUSION: LT was best predicted by the measured lowest VE/VO2 and the plot of the ln [LA-] to ln VO2 relationship. The methods used in this study provide a valid estimate of the LT and support the use of measured lowest VE/VO2 as an indirect measure of the LT.

Acidosis, Lactic↗

Concentrations of lactate and pyruvate and temperature effects on lactate dehydrogenase activity in the tissues of the big brown bat (Eptesicus fuscus) during arousal from hibernation.

1. The rectal temperatures, steady state concentrations of lactate and pyruvate, and the LDH isoenzyme composition in the heart, liver, and pectoral muscle of hibernating and arousing Eptesicus fuscus were measured. 2. Bat rectal temperature increased from 8.86 to 33.1 degrees C during arousal. 3. During arousal, steady state concentrations of pyruvate and lactate increased significantly in the tissues, however they remained generally below the level necessary to saturate LDH at the respective temperature. 4. The activities of the two LDH isoenzymes, M4, the predominant form in bat liver, and H4, the main form in bat heart and pectoral muscle, show substrate-dependent temperature effects described by the equation, mu = (E beta S + E alpha K t)/(K t + S). 5. Temperature effects (mu) on bat LDH activity increased during arousal but remained significantly lower than mu determined at saturating concentrations of substrate (E beta). 6. The parameters E beta-E alpha, E alpha and K tau are particularly important in describing the temperature dependence of LDH activity in tissues of the arousing bat.

Animals↗

Fluid requirements of severely burned children up to 3 years old: hypertonic lactated saline vs. Ringer's lactate-colloid.

Children with burns greater than or equal to 30 per cent of the body surface area were entered into a prospective fluid resuscitation protocol using hypertonic lactated saline (HLS) or Ringer's lactate-colloid. The two resuscitation groups were subdivided into patients less than or equal to 3 years old and children greater than 3 years old. The children under 3 years old required significantly more fluid and sodium during the first 48 h when calculations were made using body weight as the indexing factor. When fluid and sodium needs of paediatric age groups were calculated using body surface area as the indexing factor, significant differences in fluid and sodium requirements were no longer present between age groups. This suggests that these observed differences may reflect the difference in surface area to mass ratio for these age groups. Children resuscitated with HLS require 23 per cent less fluid in the first 24 h. If body weight is used for estimating fluid needs, clinicians should be aware of the differences in fluid requirements for children less than or equal to 3 years old compared with older paediatric patients. Formulas for estimating fluid needs are presented.

Blood Glucose↗

A prospective analysis of hypertonic lactated saline v. Ringer's lactate-colloid for the resuscitation of severely burned children.

Children and young people ranging in age from 5 months to 21 years, with burns covering greater than or equal to 30 per cent of the body surface area, were entered into a prospective study comparing the resuscitative efficacy of hypertonic lactated saline (HLS) and Ringer's lactate-colloid (RL-colloid). The 24- and 48-h fluid requirements of children resuscitated with the RL-colloid were significantly greater than those resuscitated with HLS (P less than 0.02); 2.37 +/- 0.91 ml/kg/per cent burn (HLS) v. 3.43 +/- 1.51 ml/kg/per cent burn (RL-colloid) at 24 h post-burn and 4.18 +/- 1.37 ml/kg/per cent burn (HLS) v. 6.32 +/- ml/kg/per cent burn (RL-colloid) at 48 h (P less than 0.01). The urine output between the two groups was not significantly different, and the haematocrits were equally maintained. Patients in the RL-colloid group gained significantly more weight at 48 h (P less than 0.05). The sodium requirements and resulting sodium balances were not significantly different. The desired and significant elevation (P less than 0.001) of serum sodium in the HLS group was maintained for the 5 days of the study. Colloid oncotic pressures, serum albumin and albumin/globulin (A/G) ratios were not significantly different between the two groups until 48 h post-burn. The RL-colloid group received plasmanate during the second 24-h period. The significant elevation in serum albumin, A/G ratio and colloid oncotic pressure persisted for only 2 days--by 96 h post-burn these values were no longer significantly different.(ABSTRACT TRUNCATED AT 250 WORDS)

Adolescent↗

The kinetics of the interconversion of intermediates of the reaction of pig muscle lactate dehydrogenase with oxidized nicotinamide-adenine dinucleotide and lactate.

Oxamate competes with pyruvate for the substrate binding site on the E(NADH) complex of pig skeletal muscle lactate dehydrogenase. When this enzyme was mixed with saturating concentrations of NAD(+) and lactate in a stopped-flow rapid-reaction spectrophotometer there was no transient accumulation of enzyme complexes with the reduced nucleotide. The steady-state rate of formation of free NADH was reached within the dead-time of the instrument (3ms). When oxamate was added to inhibit the steady state and to uncouple the equilibration: [Formula: see text] through the rapid formation of E(NADH) (Oxamate), the rate of formation of E(NADH) could be measured by observation of the first turnover. This pH-dependent transient is controlled by the rate of dissociation of pyruvate and the fraction of the enzyme in the form E(NADH) (Pyruvate).

Animals↗