Effects of liposomal-curcumin on five opportunistic bacterial strains found in the equine hindgut - preliminary study

The in vitro 24 h batch culture examined the effect of dose on bacteria concentrations when supplementing liposomal-curcumin (LIPC). Sixteen 125 mL Erhlenmeyer flasks were randomly assigned one of the following treatments in quadruplicate: 1) LIPC at the recommended dose of 15 g, (15); 2) 20 g of LIPC, (20); 3) 25 g of LIPC (25); or 4) 30 g of LIPC, (30). Based on the recommended dosage of 500 mg/g of turmeric at 15 g per 454.54 kg horse [10], the selected treatments were increased by 5 g, up to twice the recommended dose.

Composited cecal fluid mixed with McDougall’s buffer, at a 1:4 ratio [12], was poured (50 mL) into 16 separate 125 mL Erlenmeyer flasks, degassed with carbon dioxide (CO₂), and placed in a water bath at 39 °C. The 125 mL Erlenmeyer flasks also contained 0.50 g [14] of ground alfalfa hay. Flasks were manually shaken every 2 h for 24 h.

Samples were collected at 0 and 24 h, pH measured (Oakton pH 110 Advanced Portable Meter (Vernon Hills, IL), stored in a 15 mL conical tube, and frozen at −80 °C for later analysis, including deoxyribonucleic acid (DNA) extraction (PowerSoil Mo Bio DNA Extraction Kits (Mo Bio Laboratories, Carlsbad, CA) and qPCR (Bio-Rad MyiQ Optical System Software 2.0). A Nano Drop ND-1000 Spectrophotometer (Wilmington, DW) assessed all DNA extractions for concentration and quality prior to PCR.

Performed in triplicates, all real-time PCR runs and each reaction mixture was prepared using Maxima SYBR Green/ROX qPCR (Thermo Scientific, Waltham, MA). The five opportunistic bacteria, E. coli general and K-12 [15] C. difficile [16, 17], C. perfringens [18], and SBEC [19] were amplified using a CFX96 Touch Real-Time PCR Detection System (Bio-Rad Laboratories, Inc., Hercules, CA), quantity analysis was performed by calculating the absolute value, using the cycle threshold. The primers sequences used are in Table 1.

Four cecally-cannulated horses were utilized in a 4 × 4 Latin square to evaluate increasing doses of LIPC on the concentrations of the same opportunistic bacteria stated in the in vitro and to examine cecal characteristics, such as volatile fatty acids (VFA) and ammonia nitrate (NH₃) concentrations. One of four treatments: 1) no LIPC, (0); 2) 15 g LIPC, recommended dose, (15); 3) 25 g LIPC (25); or 4) 35 g LIPC (35) for a total of 7500 mg, 12,500 mg, and 17,500 mg, respectively, of the active ingredient dosed daily, were randomly assigned to horses. Horses were fed 0.90-1.36 kg of Strategy® (Purina Mills, St. Louis, MO), once daily at 0600 and the treatments were top-dressed on the grain, for delivery and to maintain a BCS of 5-6. Post grain and treatment consumption, horses were then turned out to pasture (predominantly K31 Tall Fescue) and allowed to graze until 1600. This was the daily procedure with the exception for d 9 of each period, during which they were stalled all day and had ab libitum access to hay and water after complete consumption of Strategy® and treatment.

Each period was 14 days with a 9 d acclimation period and a 5 d withdrawal period [10, 20]. Cecal fluid was collected at 0 h on d 0 and 8, and again on d 9 at 0, 3, 6, 9, 12, 15, 18, and 21 h. Whole cecal contents (100 mL) were collected, pH recorded (Oakton pH 110 Advanced Portable Meter (Vernon Hills, IL), subsampled (15 mL), and immediately frozen for later analysis of opportunistic bacteria. On d nine, after pH was recorded, contents were filtered through eight layers of cheesecloth into a 15 mL collection tube and immediately frozen for later analysis of VFA and ammonia concentrations. Cecal NH₃ concentrations were determined by the phenol-hypochlorite procedure [21]. VFA concentrations were determined [22] using a Shimadzu GC-2010 gas chromatograph (Shimadzu Scientific Instruments, Inc., Columbia, MD) and internal standards made with 2-ethyl butyrate [22].

Blood was also collected via jugular venipuncture on d 0 and 8 into a vacutainer serum separator tube and a 7.5% Ethylenediaminetetraacetic acid (EDTA) tube (Coviden, Mansfield, MA) for chemistry panel analysis, and complete blood count analysis, respectively.

The bacterial concentrations from in vitro experiment were analyzed as a completely randomized design using the MIXED procedure of SAS (SAS 9.4 Inst., Inc., Cary, NC).

For the in vivo experiment, bacterial concentrations, chemistry panel data, and complete blood count data were analyzed using the MIXED procedure of SAS (SAS 9.4 Inst., Inc., Cary, NC) using the model for a Latin square design with a Tukey post-hoc adjustment. Cecal fermentation data (NH₃, pH, and VFA) were analyzed using the MIXED procedure of SAS for repeated measures. An autoregressive covariance structure (AR1 of the MIXED procedure of SAS) was determined to be most appropriate based on Akaike’s Information Criterion. Comparisons of main effects were determined using least square means and Fisher’s protected LSD. Calculation of coefficients for linear orthogonal polynomials with unequal spacing was done using IML of SAS [23]. Significance was set at (P ≤ 0.05) and tendency was set at (P ≤ 0.10).

The bacteria concentrations for the in vitro study are summarized in Table 2. Every flask had a pH within the normal equine cecum pH range of 6.5-7.1 [24]. Concentrations of SBEC were significantly lower (P < 0.0001) at the recommended dose (15) when compared to the 20, 25, and 30 dose treatments. E. coli substrain K-12 concentrations increased (P = 0.01) in the 25 and 30 treatments compared to 15 and 20 treatments. Concentrations of E. coli general were significantly less (P = 0.03) for 15, 20, and 30 compared to the 25 treatment.

Based on the results of the batch culture, the authors decided to investigate 15 g, 25 g, and 35 g of 95% LIPC. SBEC bacterial concentrations increased linearly (P = 0.008) as LIPC dose increased (Table 3). However, as the dose of LIPC increased, the concentration of C. perfringens decreased linearly (P = 0.03).

Cecal fluid pH and ammonia concentration were not significant among treatments (P = 0.82) and (P = 0.21), respectively (Table 3). However, ammonia concentrations decreased numerically in a linear fashion as LIPC dose increased. Valerate was significantly different (P = 0.02) among treatments with 0 having the greatest concentration compared to all other treatments. Moreover, valerate decreased linearly (P = 0.005) as LIPC dose increased. As LIPC dose increased, butyrate and iso-valerate decreased linearly (P ≤ 0.03). However, acetate tended to increase linearly (P < 0.10), as the dose of LIPC increased. Lastly, increasing doses of LIPC tended (P = 0.10) to linearly increase total VFA concentrations when compared to 0.

Previous work, with human subjects, showed E. coli substrain K-12 possesses curcumin-converting activity, allowing this substrain to utilize curcumin as a substrate for growth [8]. It is possible that in the current study, increasing the dosage of LIPC increased the concentration of curcumin that E. coli general and K-12 could utilize as a substrate thus, allowing for an increase in these bacterial concentrations.

Although increasing the dose of LIPC decreased C. perfringens, the observation that increasing the dose also increases SBEC and C. difficile would suggest that there may be no additional benefit of dosing LIPC above the recommended rate and could lead to potential problems, such as an dysbiosis of the hindgut microbiota leading to colic, diarrhea, and enterocolitis. In addition, this would also suggest that the nutraceutical is not compromised in the stomach or small intestine during the digestion process before reaching the cecum.

The tendencies to increase acetate and total VFAs would suggest that a longer dosing period of LIPC might increase fiber digestibility [25]; however, a decrease in butyrate may decrease intestinal lining repair. In addition, when dosing higher than the recommended dose (15 g) for long periods, caretakers should take caution. The numerical decrease in ammonia and isobuytrate along with a decrease in isovalerate suggests that rate of protein degradation may decrease when LIPC is administered above the recommended dose for longer periods.